http://togogenome.org/gene/1863:CKV89_RS08890 ^@ http://purl.uniprot.org/uniprot/A0A239VMT5 ^@ Similarity ^@ Belongs to the glutamine synthetase family. http://togogenome.org/gene/1863:CKV89_RS05205 ^@ http://purl.uniprot.org/uniprot/A0A239VEP2 ^@ Similarity ^@ Belongs to the bacterial ribosomal protein bS16 family. http://togogenome.org/gene/1863:CKV89_RS05495 ^@ http://purl.uniprot.org/uniprot/A0A239VF83 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the RbfA family.|||Cytoplasm|||Monomer. Binds 30S ribosomal subunits, but not 50S ribosomal subunits or 70S ribosomes.|||One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA. http://togogenome.org/gene/1863:CKV89_RS09740 ^@ http://purl.uniprot.org/uniprot/A0A239VR56 ^@ Function|||Similarity ^@ Belongs to the RmuC family.|||Involved in DNA recombination. http://togogenome.org/gene/1863:CKV89_RS09985 ^@ http://purl.uniprot.org/uniprot/A0A239VS13 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. EF-G/EF-2 subfamily.|||Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post-translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS05860 ^@ http://purl.uniprot.org/uniprot/A0A239VHC9 ^@ Function|||Similarity ^@ Belongs to the RecN family.|||May be involved in recombinational repair of damaged DNA. http://togogenome.org/gene/1863:CKV89_RS02625 ^@ http://purl.uniprot.org/uniprot/A0A239V9S9 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS06950 ^@ http://purl.uniprot.org/uniprot/A0A239VJ95 ^@ Cofactor ^@ Binds 1 zinc ion per subunit. http://togogenome.org/gene/1863:CKV89_RS01890 ^@ http://purl.uniprot.org/uniprot/A0A239V7Y7 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the UreE family.|||Cytoplasm|||Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly. http://togogenome.org/gene/1863:CKV89_RS09900 ^@ http://purl.uniprot.org/uniprot/A0A239VRE0 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS8 family.|||One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit.|||Part of the 30S ribosomal subunit. Contacts proteins S5 and S12. http://togogenome.org/gene/1863:CKV89_RS09950 ^@ http://purl.uniprot.org/uniprot/A0A239VQ98 ^@ Function|||Similarity ^@ Belongs to the universal ribosomal protein uS19 family.|||Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA. http://togogenome.org/gene/1863:CKV89_RS09320 ^@ http://purl.uniprot.org/uniprot/A0A239VQ77 ^@ Similarity ^@ Belongs to the CobH/CbiC family. http://togogenome.org/gene/1863:CKV89_RS05775 ^@ http://purl.uniprot.org/uniprot/A0A239VHR8 ^@ Similarity ^@ Belongs to the bacterial ribosomal protein bL35 family. http://togogenome.org/gene/1863:CKV89_RS06035 ^@ http://purl.uniprot.org/uniprot/A0A239VGQ8 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the elongation factor P family.|||Cytoplasm|||Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase. http://togogenome.org/gene/1863:CKV89_RS05300 ^@ http://purl.uniprot.org/uniprot/A0A239VFV4 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF-Tu.GTP complex up to the GTP hydrolysis stage on the ribosome.|||Belongs to the EF-Ts family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS02225 ^@ http://purl.uniprot.org/uniprot/A0A239V928 ^@ Function|||Similarity|||Subunit ^@ Belongs to the bacterial ribosomal protein bS18 family.|||Binds as a heterodimer with protein bS6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit.|||Part of the 30S ribosomal subunit. Forms a tight heterodimer with protein bS6. http://togogenome.org/gene/1863:CKV89_RS05295 ^@ http://purl.uniprot.org/uniprot/A0A239VGC9 ^@ Similarity ^@ Belongs to the universal ribosomal protein uS2 family. http://togogenome.org/gene/1863:CKV89_RS09825 ^@ http://purl.uniprot.org/uniprot/A0A239VPV5 ^@ Caution|||Function|||Similarity|||Subunit ^@ Belongs to the tRNA pseudouridine synthase TruA family.|||Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs.|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS01080 ^@ http://purl.uniprot.org/uniprot/A0A239V6H2 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family.|||Cell membrane http://togogenome.org/gene/1863:CKV89_RS10600 ^@ http://purl.uniprot.org/uniprot/A0A239VSB7 ^@ Similarity ^@ Belongs to the NAD synthetase family. http://togogenome.org/gene/1863:CKV89_RS10290 ^@ http://purl.uniprot.org/uniprot/A0A239VSM2 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the complex I 30 kDa subunit family.|||Cell membrane|||NDH-1 is composed of 14 different subunits. Subunits NuoB, C, D, E, F, and G constitute the peripheral sector of the complex.|||NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be a menaquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. http://togogenome.org/gene/1863:CKV89_RS03320 ^@ http://purl.uniprot.org/uniprot/A0A239VC48 ^@ Function|||Similarity ^@ Belongs to the uroporphyrinogen-III synthase family.|||Catalyzes cyclization of the linear tetrapyrrole, hydroxymethylbilane, to the macrocyclic uroporphyrinogen III. http://togogenome.org/gene/1863:CKV89_RS08000 ^@ http://purl.uniprot.org/uniprot/A0A239VM17 ^@ Similarity|||Subunit ^@ Belongs to the class-II aminoacyl-tRNA synthetase family.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS04970 ^@ http://purl.uniprot.org/uniprot/A0A239VEH2 ^@ Similarity ^@ Belongs to the phosphohexose mutase family. http://togogenome.org/gene/1863:CKV89_RS08700 ^@ http://purl.uniprot.org/uniprot/A0A239VNL6 ^@ Similarity ^@ Belongs to the acetyl-CoA hydrolase/transferase family. http://togogenome.org/gene/1863:CKV89_RS03650 ^@ http://purl.uniprot.org/uniprot/A0A239VDA4 ^@ Similarity ^@ Belongs to the peptidase A24 family. http://togogenome.org/gene/1863:CKV89_RS09600 ^@ http://purl.uniprot.org/uniprot/A0A239VPE6 ^@ Subcellular Location Annotation ^@ Endoplasmic reticulum membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS04630 ^@ http://purl.uniprot.org/uniprot/A0A239VDG3 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the ATPase gamma chain family.|||Cell membrane|||F-type ATPases have 2 components, CF(1) - the catalytic core - and CF(0) - the membrane proton channel. CF(1) has five subunits: alpha(3), beta(3), gamma(1), delta(1), epsilon(1). CF(0) has three main subunits: a, b and c.|||Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex. http://togogenome.org/gene/1863:CKV89_RS07440 ^@ http://purl.uniprot.org/uniprot/A0A239VL47 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation ^@ Cytoplasm|||In the C-terminal section; belongs to the phosphate acetyltransferase and butyryltransferase family.|||In the N-terminal section; belongs to the CobB/CobQ family.|||Involved in acetate metabolism.|||The N-terminal region seems to be important for proper quaternary structure. The C-terminal region contains the substrate-binding site. http://togogenome.org/gene/1863:CKV89_RS07915 ^@ http://purl.uniprot.org/uniprot/A0A239VKZ4 ^@ Caution|||Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the CDP-alcohol phosphatidyltransferase class-I family.|||Catalyzes the conjugation of the 1'-hydroxyl group of D-myo-inositol-3-phosphate (also named L-myo-inositol-1-phosphate) with a lipid tail of cytidine diphosphate diacylglycerol (CDP-DAG), forming phosphatidylinositol phosphate (PIP) and CMP. PIP is a precursor of phosphatidylinositol (PI) which is an essential lipid required for cell wall formation.|||Cell membrane|||Contains a di-nuclear catalytic Mg(2+) center.|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Membrane http://togogenome.org/gene/1863:CKV89_RS10565 ^@ http://purl.uniprot.org/uniprot/A0A239VSJ7 ^@ Similarity ^@ Belongs to the CsoR family. http://togogenome.org/gene/1863:CKV89_RS04270 ^@ http://purl.uniprot.org/uniprot/A0A239VD01 ^@ Function|||Similarity ^@ Belongs to the phosphoglycerate mutase family. BPG-dependent PGAM subfamily.|||Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate. http://togogenome.org/gene/1863:CKV89_RS07185 ^@ http://purl.uniprot.org/uniprot/A0A239VJL1 ^@ Caution|||Similarity|||Subcellular Location Annotation ^@ Belongs to the class-I aminoacyl-tRNA synthetase family.|||Cytoplasm|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS00315 ^@ http://purl.uniprot.org/uniprot/A0A239V5K6 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily.|||Membrane http://togogenome.org/gene/1863:CKV89_RS05125 ^@ http://purl.uniprot.org/uniprot/A0A239VG03 ^@ Caution|||Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the FPG family.|||Binds 1 zinc ion per subunit.|||Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic/apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Monomer. http://togogenome.org/gene/1863:CKV89_RS05175 ^@ http://purl.uniprot.org/uniprot/A0A239VFW5 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the GTP-binding SRP family. SRP54 subfamily.|||Composed of three domains: the N-terminal N domain, which is responsible for interactions with the ribosome, the central G domain, which binds GTP, and the C-terminal M domain, which binds the RNA and the signal sequence of the RNC.|||Cytoplasm|||Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY.|||Part of the signal recognition particle protein translocation system, which is composed of SRP and FtsY. http://togogenome.org/gene/1863:CKV89_RS09870 ^@ http://purl.uniprot.org/uniprot/A0A239VRG0 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the SecY/SEC61-alpha family.|||Cell membrane|||Component of the Sec protein translocase complex. Heterotrimer consisting of SecY, SecE and SecG subunits. The heterotrimers can form oligomers, although 1 heterotrimer is thought to be able to translocate proteins. Interacts with the ribosome. Interacts with SecDF, and other proteins may be involved. Interacts with SecA.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Membrane|||The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently. http://togogenome.org/gene/1863:CKV89_RS10025 ^@ http://purl.uniprot.org/uniprot/A0A239VRP4 ^@ Function|||PTM|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL11 family.|||Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors.|||One or more lysine residues are methylated.|||Part of the ribosomal stalk of the 50S ribosomal subunit. Interacts with L10 and the large rRNA to form the base of the stalk. L10 forms an elongated spine to which L12 dimers bind in a sequential fashion forming a multimeric L10(L12)X complex. http://togogenome.org/gene/1863:CKV89_RS04200 ^@ http://purl.uniprot.org/uniprot/A0A239VDK0 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family. CysTW subfamily.|||Cell membrane|||Membrane|||Part of the binding-protein-dependent transport system for phosphate; probably responsible for the translocation of the substrate across the membrane. http://togogenome.org/gene/1863:CKV89_RS09885 ^@ http://purl.uniprot.org/uniprot/A0A239VRC2 ^@ Domain|||Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS5 family.|||Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body.|||Part of the 30S ribosomal subunit. Contacts proteins S4 and S8.|||The N-terminal domain interacts with the head of the 30S subunit; the C-terminal domain interacts with the body and contacts protein S4. The interaction surface between S4 and S5 is involved in control of translational fidelity.|||With S4 and S12 plays an important role in translational accuracy. http://togogenome.org/gene/1863:CKV89_RS10760 ^@ http://purl.uniprot.org/uniprot/A0A239VSS1 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the MscL family.|||Cell membrane|||Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell.|||Homopentamer.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Membrane http://togogenome.org/gene/1863:CKV89_RS00040 ^@ http://purl.uniprot.org/uniprot/A0A239V2H3 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the ClpA/ClpB family.|||Cytoplasm|||Homohexamer. The oligomerization is ATP-dependent.|||Homohexamer; The oligomerization is ATP-dependent.|||Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE. http://togogenome.org/gene/1863:CKV89_RS00850 ^@ http://purl.uniprot.org/uniprot/A0A239V5V5 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS08925 ^@ http://purl.uniprot.org/uniprot/A0A239VND8 ^@ Function ^@ Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle. http://togogenome.org/gene/1863:CKV89_RS12490 ^@ http://purl.uniprot.org/uniprot/A0A239VCG6 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS05210 ^@ http://purl.uniprot.org/uniprot/A0A239VFB2 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ A probable RNA-binding protein.|||Belongs to the KhpA RNA-binding protein family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS07580 ^@ http://purl.uniprot.org/uniprot/A0A239VKA7 ^@ Subcellular Location Annotation ^@ Cytoplasm http://togogenome.org/gene/1863:CKV89_RS05795 ^@ http://purl.uniprot.org/uniprot/A0A239VGG1 ^@ Cofactor|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily.|||Binds 2 magnesium ions per tetramer.|||Cytoplasm|||Tetramer of two alpha and two beta subunits. http://togogenome.org/gene/1863:CKV89_RS01465 ^@ http://purl.uniprot.org/uniprot/A0A239V708 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS10170 ^@ http://purl.uniprot.org/uniprot/A0A239VQY8 ^@ Similarity ^@ Belongs to the bacterial ribosomal protein bL28 family. http://togogenome.org/gene/1863:CKV89_RS09920 ^@ http://purl.uniprot.org/uniprot/A0A239VRW5 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL14 family.|||Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome.|||Part of the 50S ribosomal subunit. Forms a cluster with proteins L3 and L19. In the 70S ribosome, L14 and L19 interact and together make contacts with the 16S rRNA in bridges B5 and B8. http://togogenome.org/gene/1863:CKV89_RS04765 ^@ http://purl.uniprot.org/uniprot/A0A239VE09 ^@ Similarity ^@ Belongs to the AB hydrolase superfamily. Lipase family. http://togogenome.org/gene/1863:CKV89_RS02190 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UGI1 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS03475 ^@ http://purl.uniprot.org/uniprot/A0A239VBH9 ^@ Function|||Similarity|||Subunit ^@ Belongs to the dTDP-4-dehydrorhamnose 3,5-epimerase family.|||Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4-hexulose.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS08620 ^@ http://purl.uniprot.org/uniprot/A0A239VNA6 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the transaldolase family. Type 2 subfamily.|||Cytoplasm|||Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway. http://togogenome.org/gene/1863:CKV89_RS01870 ^@ http://purl.uniprot.org/uniprot/A0A239V7G4 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the urea transporter family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS01990 ^@ http://purl.uniprot.org/uniprot/A0A239V7N9 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family.|||Cell membrane http://togogenome.org/gene/1863:CKV89_RS01140 ^@ http://purl.uniprot.org/uniprot/A0A239V878 ^@ Function ^@ Catalyzes the phosphorylation of hydroxymethylpyrimidine phosphate (HMP-P) to HMP-PP, and of HMP to HMP-P. http://togogenome.org/gene/1863:CKV89_RS02355 ^@ http://purl.uniprot.org/uniprot/A0A239V8W3 ^@ Similarity ^@ Belongs to the GMC oxidoreductase family. http://togogenome.org/gene/1863:CKV89_RS07180 ^@ http://purl.uniprot.org/uniprot/A0A239VKI7 ^@ Function|||Similarity ^@ Belongs to the bacterial ribosomal protein bS20 family.|||Binds directly to 16S ribosomal RNA. http://togogenome.org/gene/1863:CKV89_RS08235 ^@ http://purl.uniprot.org/uniprot/A0A239VN08 ^@ Similarity ^@ Belongs to the peptidase T1A family. http://togogenome.org/gene/1863:CKV89_RS06525 ^@ http://purl.uniprot.org/uniprot/A0A239VIP8 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the metallo-dependent hydrolases superfamily. HutI family.|||Binds 1 zinc or iron ion per subunit.|||Catalyzes the hydrolytic cleavage of the carbon-nitrogen bond in imidazolone-5-propanoate to yield N-formimidoyl-L-glutamate. It is the third step in the universal histidine degradation pathway.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS08655 ^@ http://purl.uniprot.org/uniprot/A0A239VN48 ^@ Function|||Similarity ^@ Belongs to the WhiA family.|||Involved in cell division and chromosome segregation. http://togogenome.org/gene/1863:CKV89_RS06335 ^@ http://purl.uniprot.org/uniprot/A0A239VIT7 ^@ Cofactor|||Similarity ^@ Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family.|||Binds 1 FAD per subunit. http://togogenome.org/gene/1863:CKV89_RS00050 ^@ http://purl.uniprot.org/uniprot/A0A239V2T6 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the MetA family.|||Cytoplasm|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Transfers an acetyl group from acetyl-CoA to L-homoserine, forming acetyl-L-homoserine. http://togogenome.org/gene/1863:CKV89_RS06955 ^@ http://purl.uniprot.org/uniprot/A0A239VKE7 ^@ Similarity ^@ Belongs to the Mg-chelatase subunits D/I family. http://togogenome.org/gene/1863:CKV89_RS09940 ^@ http://purl.uniprot.org/uniprot/A0A239VRX6 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS3 family.|||Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation.|||Part of the 30S ribosomal subunit. Forms a tight complex with proteins S10 and S14. http://togogenome.org/gene/1863:CKV89_RS07050 ^@ http://purl.uniprot.org/uniprot/A0A239VKE4 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the thymidylate synthase family. Bacterial-type ThyA subfamily.|||Catalyzes the reductive methylation of 2'-deoxyuridine-5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis.|||Cytoplasm|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS06520 ^@ http://purl.uniprot.org/uniprot/A0A239VIU7 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the urocanase family.|||Binds 1 NAD(+) per subunit.|||Catalyzes the conversion of urocanate to 4-imidazolone-5-propionate.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS09975 ^@ http://purl.uniprot.org/uniprot/A0A239VS05 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS10 family.|||Involved in the binding of tRNA to the ribosomes.|||Part of the 30S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS06585 ^@ http://purl.uniprot.org/uniprot/A0A239VIZ1 ^@ Function|||Similarity|||Subunit ^@ Belongs to the RNase PH family.|||Homohexameric ring arranged as a trimer of dimers.|||Phosphorolytic 3'-5' exoribonuclease that plays an important role in tRNA 3'-end maturation. Removes nucleotide residues following the 3'-CCA terminus of tRNAs; can also add nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates, but this may not be physiologically important. Probably plays a role in initiation of 16S rRNA degradation (leading to ribosome degradation) during starvation. http://togogenome.org/gene/1863:CKV89_RS09250 ^@ http://purl.uniprot.org/uniprot/A0A239VNI3 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Associates with subunits I, II and III to form cytochrome c oxidase.|||Belongs to the cytochrome c oxidase bacterial subunit CtaF family.|||Cell membrane|||Membrane|||Part of cytochrome c oxidase, its function is unknown. http://togogenome.org/gene/1863:CKV89_RS01730 ^@ http://purl.uniprot.org/uniprot/A0A239V750 ^@ Similarity|||Subunit ^@ Belongs to the glutaminase family.|||Homotetramer. http://togogenome.org/gene/1863:CKV89_RS01580 ^@ http://purl.uniprot.org/uniprot/A0A239V952 ^@ Function ^@ Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate. http://togogenome.org/gene/1863:CKV89_RS07955 ^@ http://purl.uniprot.org/uniprot/A0A239VM05 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the RuvC family.|||Binds 2 Mg(2+) ion per subunit.|||Cytoplasm|||Homodimer which binds Holliday junction (HJ) DNA. The HJ becomes 2-fold symmetrical on binding to RuvC with unstacked arms; it has a different conformation from HJ DNA in complex with RuvA. In the full resolvosome a probable DNA-RuvA(4)-RuvB(12)-RuvC(2) complex forms which resolves the HJ.|||The RuvA-RuvB-RuvC complex processes Holliday junction (HJ) DNA during genetic recombination and DNA repair. Endonuclease that resolves HJ intermediates. Cleaves cruciform DNA by making single-stranded nicks across the HJ at symmetrical positions within the homologous arms, yielding a 5'-phosphate and a 3'-hydroxyl group; requires a central core of homology in the junction. The consensus cleavage sequence is 5'-(A/T)TT(C/G)-3'. Cleavage occurs on the 3'-side of the TT dinucleotide at the point of strand exchange. HJ branch migration catalyzed by RuvA-RuvB allows RuvC to scan DNA until it finds its consensus sequence, where it cleaves and resolves the cruciform DNA. http://togogenome.org/gene/1863:CKV89_RS10605 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YT91 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS03510 ^@ http://purl.uniprot.org/uniprot/A0A239VBI5 ^@ Similarity ^@ Belongs to the carotenoid/retinoid oxidoreductase family. http://togogenome.org/gene/1863:CKV89_RS03430 ^@ http://purl.uniprot.org/uniprot/A0A239VBY6 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the chaperonin (HSP60) family.|||Cell surface|||Cytoplasm|||Forms a cylinder of 14 subunits composed of two heptameric rings stacked back-to-back. Interacts with the co-chaperonin GroES.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Together with its co-chaperonin GroES, plays an essential role in assisting protein folding. The GroEL-GroES system forms a nano-cage that allows encapsulation of the non-native substrate proteins and provides a physical environment optimized to promote and accelerate protein folding.|||capsule|||cell wall http://togogenome.org/gene/1863:CKV89_RS01845 ^@ http://purl.uniprot.org/uniprot/A0A239V7G7 ^@ Caution ^@ Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS05540 ^@ http://purl.uniprot.org/uniprot/A0A239VHR5 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS02240 ^@ http://purl.uniprot.org/uniprot/A0A239V8P3 ^@ Function|||Similarity ^@ Belongs to the helicase family. DnaB subfamily.|||Participates in initiation and elongation during chromosome replication; it exhibits DNA-dependent ATPase activity. http://togogenome.org/gene/1863:CKV89_RS09880 ^@ http://purl.uniprot.org/uniprot/A0A239VQ40 ^@ Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL30 family.|||Part of the 50S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS05890 ^@ http://purl.uniprot.org/uniprot/A0A239VGQ6 ^@ Similarity ^@ Belongs to the GMC oxidoreductase family. http://togogenome.org/gene/1863:CKV89_RS10330 ^@ http://purl.uniprot.org/uniprot/A0A239VRI8 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the KAE1 / TsaD family.|||Binds 1 Fe(2+) ion per subunit.|||Cytoplasm|||Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction. http://togogenome.org/gene/1863:CKV89_RS09690 ^@ http://purl.uniprot.org/uniprot/A0A239VPG0 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the UPF0126 family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS08885 ^@ http://purl.uniprot.org/uniprot/A0A239VPC6 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS12085 ^@ http://purl.uniprot.org/uniprot/A0A239VJE4 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the DapA family.|||Catalyzes the condensation of (S)-aspartate-beta-semialdehyde [(S)-ASA] and pyruvate to 4-hydroxy-tetrahydrodipicolinate (HTPA).|||Cytoplasm|||Homotetramer; dimer of dimers.|||Was originally thought to be a dihydrodipicolinate synthase (DHDPS), catalyzing the condensation of (S)-aspartate-beta-semialdehyde [(S)-ASA] and pyruvate to dihydrodipicolinate (DHDP). However, it was shown in E.coli that the product of the enzymatic reaction is not dihydrodipicolinate but in fact (4S)-4-hydroxy-2,3,4,5-tetrahydro-(2S)-dipicolinic acid (HTPA), and that the consecutive dehydration reaction leading to DHDP is not spontaneous but catalyzed by DapB. http://togogenome.org/gene/1863:CKV89_RS05715 ^@ http://purl.uniprot.org/uniprot/A0A239VHU0 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS08085 ^@ http://purl.uniprot.org/uniprot/A0A239VMI2 ^@ Function|||Similarity|||Subunit ^@ Belongs to the GcvP family.|||The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein.|||The glycine cleavage system is composed of four proteins: P, T, L and H. http://togogenome.org/gene/1863:CKV89_RS10675 ^@ http://purl.uniprot.org/uniprot/A0A239VUE2 ^@ Function|||Similarity ^@ Belongs to the GHMP kinase family. IspE subfamily.|||Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol. http://togogenome.org/gene/1863:CKV89_RS01285 ^@ http://purl.uniprot.org/uniprot/A0A239V6L0 ^@ Similarity ^@ Belongs to the Dps family. http://togogenome.org/gene/1863:CKV89_RS07675 ^@ http://purl.uniprot.org/uniprot/A0A239VLI9 ^@ Similarity ^@ Belongs to the thioesterase family. http://togogenome.org/gene/1863:CKV89_RS02180 ^@ http://purl.uniprot.org/uniprot/A0A239VA45 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS04155 ^@ http://purl.uniprot.org/uniprot/A0A239VCN8 ^@ Similarity ^@ Belongs to the aldehyde dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS07080 ^@ http://purl.uniprot.org/uniprot/A0A239VKI9 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the methylthiotransferase family. RimO subfamily.|||Binds 2 [4Fe-4S] clusters. One cluster is coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine.|||Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein uS12.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS03550 ^@ http://purl.uniprot.org/uniprot/A0A239VBS6 ^@ Similarity ^@ Belongs to the IMPDH/GMPR family. http://togogenome.org/gene/1863:CKV89_RS04720 ^@ http://purl.uniprot.org/uniprot/A0A239VDV6 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the NucS endonuclease family.|||Cleaves both 3' and 5' ssDNA extremities of branched DNA structures.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS04700 ^@ http://purl.uniprot.org/uniprot/A0A239VDP5 ^@ Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the ATPase epsilon chain family.|||Cell membrane|||F-type ATPases have 2 components, CF(1) - the catalytic core - and CF(0) - the membrane proton channel. CF(1) has five subunits: alpha(3), beta(3), gamma(1), delta(1), epsilon(1). CF(0) has three main subunits: a, b and c. http://togogenome.org/gene/1863:CKV89_RS04465 ^@ http://purl.uniprot.org/uniprot/A0A239VE88 ^@ Similarity ^@ Belongs to the helicase family. RAD25/XPB subfamily. http://togogenome.org/gene/1863:CKV89_RS09815 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YTG3 ^@ Caution|||Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL13 family.|||Part of the 50S ribosomal subunit.|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data.|||This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly. http://togogenome.org/gene/1863:CKV89_RS00735 ^@ http://purl.uniprot.org/uniprot/A0A239V4Q5 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS00895 ^@ http://purl.uniprot.org/uniprot/A0A239V776 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the NrfD family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS05500 ^@ http://purl.uniprot.org/uniprot/A0A239VFT2 ^@ Function|||Similarity ^@ Belongs to the pseudouridine synthase TruB family. Type 1 subfamily.|||Responsible for synthesis of pseudouridine from uracil-55 in the psi GC loop of transfer RNAs. http://togogenome.org/gene/1863:CKV89_RS06330 ^@ http://purl.uniprot.org/uniprot/A0A239VI96 ^@ Similarity ^@ Belongs to the PGI/PMI family. http://togogenome.org/gene/1863:CKV89_RS05360 ^@ http://purl.uniprot.org/uniprot/A0A239VEU8 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the peptidase M50B family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS09665 ^@ http://purl.uniprot.org/uniprot/A0A239VQW6 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ A 50S ribosomal subunit assembly protein with GTPase activity, required for 50S subunit assembly at low temperatures, may also play a role in translation. Binds GTP and analogs. Binds the 70S ribosome between the 30S and 50S subunits, in a similar position as ribosome-bound EF-G; it contacts a number of ribosomal proteins, both rRNAs and the A-site tRNA.|||Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. BipA subfamily.|||Cytoplasm|||Monomer. http://togogenome.org/gene/1863:CKV89_RS02605 ^@ http://purl.uniprot.org/uniprot/A0A239VAP0 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS00865 ^@ http://purl.uniprot.org/uniprot/A0A239V549 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS11310 ^@ http://purl.uniprot.org/uniprot/A0A239VVT4 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Bacterial flagellum|||Belongs to the bacterial flagellin family.|||Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella.|||Secreted http://togogenome.org/gene/1863:CKV89_RS03200 ^@ http://purl.uniprot.org/uniprot/A0A239VAS2 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the tRNA(Ile)-lysidine synthase family.|||Cytoplasm|||Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine.|||The N-terminal region contains the highly conserved SGGXDS motif, predicted to be a P-loop motif involved in ATP binding. http://togogenome.org/gene/1863:CKV89_RS10185 ^@ http://purl.uniprot.org/uniprot/A0A239VSC0 ^@ Similarity ^@ Belongs to the bacterial ribosomal protein bL36 family. http://togogenome.org/gene/1863:CKV89_RS09980 ^@ http://purl.uniprot.org/uniprot/A0A239VS21 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. EF-Tu/EF-1A subfamily.|||Cytoplasm|||Monomer.|||This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis. http://togogenome.org/gene/1863:CKV89_RS04005 ^@ http://purl.uniprot.org/uniprot/A0A239VD14 ^@ Similarity ^@ Belongs to the Orn/Lys/Arg decarboxylase class-II family. http://togogenome.org/gene/1863:CKV89_RS00995 ^@ http://purl.uniprot.org/uniprot/A0A239V607 ^@ Function|||Similarity ^@ Belongs to the catalase family. HPII subfamily.|||Serves to protect cells from the toxic effects of hydrogen peroxide. http://togogenome.org/gene/1863:CKV89_RS08595 ^@ http://purl.uniprot.org/uniprot/A0A239VLU4 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the ABC-2 integral membrane protein family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS04625 ^@ http://purl.uniprot.org/uniprot/A0A239VDD6 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the ATPase alpha/beta chains family.|||Cell membrane|||Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit. http://togogenome.org/gene/1863:CKV89_RS04635 ^@ http://purl.uniprot.org/uniprot/A0A239VEY7 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the ATPase alpha/beta chains family.|||Cell membrane|||Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits. http://togogenome.org/gene/1863:CKV89_RS02455 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UEM7 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS04830 ^@ http://purl.uniprot.org/uniprot/A0A239VE48 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the MIP/aquaporin (TC 1.A.8) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS05010 ^@ http://purl.uniprot.org/uniprot/A0A239VEM2 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS06110 ^@ http://purl.uniprot.org/uniprot/A0A239VIU0 ^@ Caution|||Cofactor|||Similarity|||Subunit ^@ Belongs to the CarB family.|||Binds 4 Mg(2+) or Mn(2+) ions per subunit.|||Composed of two chains; the small (or glutamine) chain promotes the hydrolysis of glutamine to ammonia, which is used by the large (or ammonia) chain to synthesize carbamoyl phosphate.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS06555 ^@ http://purl.uniprot.org/uniprot/A0A239VIA3 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS04920 ^@ http://purl.uniprot.org/uniprot/A0A239VE94 ^@ Similarity ^@ Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family. http://togogenome.org/gene/1863:CKV89_RS07140 ^@ http://purl.uniprot.org/uniprot/A0A239VKA1 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the RecX family.|||Cytoplasm|||Modulates RecA activity. http://togogenome.org/gene/1863:CKV89_RS09845 ^@ http://purl.uniprot.org/uniprot/A0A239VQH0 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS11 family.|||Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome.|||Part of the 30S ribosomal subunit. Interacts with proteins S7 and S18. Binds to IF-3. http://togogenome.org/gene/1863:CKV89_RS01120 ^@ http://purl.uniprot.org/uniprot/A0A239V5S0 ^@ Similarity ^@ Belongs to the glycosyl hydrolase 65 family. http://togogenome.org/gene/1863:CKV89_RS06205 ^@ http://purl.uniprot.org/uniprot/A0A239VI58 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the nicotinamide ribonucleoside (NR) uptake permease (TC 4.B.1) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS04815 ^@ http://purl.uniprot.org/uniprot/A0A239VE10 ^@ Similarity ^@ Belongs to the peptidase M1 family. http://togogenome.org/gene/1863:CKV89_RS04825 ^@ http://purl.uniprot.org/uniprot/A0A239VE08 ^@ Similarity ^@ Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS05480 ^@ http://purl.uniprot.org/uniprot/A0A239VGS0 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the NusA family.|||Cytoplasm|||Monomer. Binds directly to the core enzyme of the DNA-dependent RNA polymerase and to nascent RNA.|||Participates in both transcription termination and antitermination. http://togogenome.org/gene/1863:CKV89_RS02230 ^@ http://purl.uniprot.org/uniprot/A0A239VAH7 ^@ Function|||Similarity ^@ Belongs to the bacterial ribosomal protein bL9 family.|||Binds to the 23S rRNA. http://togogenome.org/gene/1863:CKV89_RS07335 ^@ http://purl.uniprot.org/uniprot/A0A239VL74 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. LepA subfamily.|||Cell membrane|||Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back-translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner. http://togogenome.org/gene/1863:CKV89_RS03210 ^@ http://purl.uniprot.org/uniprot/A0A239VAW8 ^@ Caution|||Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins.|||Belongs to the AAA ATPase family.|||Binds 1 zinc ion per subunit.|||Cell membrane|||Homohexamer.|||In the C-terminal section; belongs to the peptidase M41 family.|||In the central section; belongs to the AAA ATPase family.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS03975 ^@ http://purl.uniprot.org/uniprot/A0A239VD38 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily.|||Membrane http://togogenome.org/gene/1863:CKV89_RS07225 ^@ http://purl.uniprot.org/uniprot/A0A239VJD4 ^@ Cofactor|||Function|||Similarity ^@ Belongs to the NrdR family.|||Binds 1 zinc ion.|||Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR-boxes. http://togogenome.org/gene/1863:CKV89_RS09580 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YT45 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS06860 ^@ http://purl.uniprot.org/uniprot/A0A239VJF1 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-I aminoacyl-tRNA synthetase family. IleS type 2 subfamily.|||Catalyzes the attachment of isoleucine to tRNA(Ile). As IleRS can inadvertently accommodate and process structurally similar amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile).|||Cytoplasm|||IleRS has two distinct active sites: one for aminoacylation and one for editing. The misactivated valine is translocated from the active site to the editing site, which sterically excludes the correctly activated isoleucine. The single editing site contains two valyl binding pockets, one specific for each substrate (Val-AMP or Val-tRNA(Ile)).|||Monomer. http://togogenome.org/gene/1863:CKV89_RS01905 ^@ http://purl.uniprot.org/uniprot/A0A239V814 ^@ Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the urease gamma subunit family.|||Cytoplasm|||Heterotrimer of UreA (gamma), UreB (beta) and UreC (alpha) subunits. Three heterotrimers associate to form the active enzyme. http://togogenome.org/gene/1863:CKV89_RS03595 ^@ http://purl.uniprot.org/uniprot/A0A239VC96 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS05250 ^@ http://purl.uniprot.org/uniprot/A0A239VG33 ^@ Function|||Similarity ^@ Belongs to the bacterial ribosomal protein bL19 family.|||This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site. http://togogenome.org/gene/1863:CKV89_RS07295 ^@ http://purl.uniprot.org/uniprot/A0A239VKQ1 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the CPA3 antiporters (TC 2.A.63) subunit E family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS04835 ^@ http://purl.uniprot.org/uniprot/A0A239VFM1 ^@ Activity Regulation|||Caution|||Function|||Similarity ^@ Belongs to the FGGY kinase family.|||Inhibited by fructose 1,6-bisphosphate (FBP).|||Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn-glycerol 3-phosphate.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS01880 ^@ http://purl.uniprot.org/uniprot/A0A239V9P3 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the SIMIBI class G3E GTPase family. UreG subfamily.|||Cytoplasm|||Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG.|||Homodimer. UreD, UreF and UreG form a complex that acts as a GTP-hydrolysis-dependent molecular chaperone, activating the urease apoprotein by helping to assemble the nickel containing metallocenter of UreC. The UreE protein probably delivers the nickel. http://togogenome.org/gene/1863:CKV89_RS10180 ^@ http://purl.uniprot.org/uniprot/A0A239VSM9 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS14 family.|||Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site.|||Part of the 30S ribosomal subunit. Contacts proteins S3 and S10. http://togogenome.org/gene/1863:CKV89_RS03585 ^@ http://purl.uniprot.org/uniprot/A0A239VD64 ^@ Caution|||Function|||Similarity|||Subunit ^@ Belongs to the MurCDEF family. MurT subfamily.|||Forms a heterodimer with GatD.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||The lipid II isoglutaminyl synthase complex catalyzes the formation of alpha-D-isoglutamine in the cell wall lipid II stem peptide. The MurT subunit catalyzes the ATP-dependent amidation of D-glutamate residue of lipid II, converting it to an isoglutamine residue. http://togogenome.org/gene/1863:CKV89_RS00420 ^@ http://purl.uniprot.org/uniprot/A0A239V4N7 ^@ Cofactor|||Similarity ^@ Belongs to the mannose-6-phosphate isomerase type 1 family.|||Binds 1 zinc ion per subunit. http://togogenome.org/gene/1863:CKV89_RS04485 ^@ http://purl.uniprot.org/uniprot/A0A239VD20 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the nucleobase:cation symporter-2 (NCS2) (TC 2.A.40) family. Azg-like subfamily.|||Membrane http://togogenome.org/gene/1863:CKV89_RS05635 ^@ http://purl.uniprot.org/uniprot/A0A239VHM8 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the MurCDEF family. MurF subfamily.|||Cytoplasm|||Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein. http://togogenome.org/gene/1863:CKV89_RS10255 ^@ http://purl.uniprot.org/uniprot/A0A239VR91 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the complex I subunit 6 family.|||Cell membrane|||NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. http://togogenome.org/gene/1863:CKV89_RS11150 ^@ http://purl.uniprot.org/uniprot/A0A239VUC5 ^@ Similarity ^@ Belongs to the MotB family. http://togogenome.org/gene/1863:CKV89_RS03090 ^@ http://purl.uniprot.org/uniprot/A0A239VAH6 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS05380 ^@ http://purl.uniprot.org/uniprot/A0A239VEY5 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the 4-toluene sulfonate uptake permease (TSUP) (TC 2.A.102) family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS08675 ^@ http://purl.uniprot.org/uniprot/A0A239VM07 ^@ Function ^@ Iron-sulfur subunit of the cytochrome bc1 complex, an essential component of the respiratory electron transport chain required for ATP synthesis. The bc1 complex catalyzes the oxidation of menaquinol and the reduction of cytochrome c in the respiratory chain. The bc1 complex operates through a Q-cycle mechanism that couples electron transfer to generation of the proton gradient that drives ATP synthesis. http://togogenome.org/gene/1863:CKV89_RS01415 ^@ http://purl.uniprot.org/uniprot/A0A239V8V1 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the amino acid-polyamine-organocation (APC) superfamily. Amino acid transporter (AAT) (TC 2.A.3.1) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS07660 ^@ http://purl.uniprot.org/uniprot/A0A239VLL0 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS04570 ^@ http://purl.uniprot.org/uniprot/A0A239VDH6 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the bacterial ribosomal protein bL31 family. Type A subfamily.|||Binds 1 zinc ion per subunit.|||Binds the 23S rRNA.|||Part of the 50S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS03190 ^@ http://purl.uniprot.org/uniprot/A0A239VAH1 ^@ Similarity ^@ Belongs to the peptidase S13 family. http://togogenome.org/gene/1863:CKV89_RS03185 ^@ http://purl.uniprot.org/uniprot/A0A239VB56 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the PPase family.|||Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions.|||Cytoplasm|||Homohexamer. http://togogenome.org/gene/1863:CKV89_RS01290 ^@ http://purl.uniprot.org/uniprot/A0A239V674 ^@ Similarity ^@ Belongs to the peptidase S8 family. http://togogenome.org/gene/1863:CKV89_RS09765 ^@ http://purl.uniprot.org/uniprot/A0A239VPQ5 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the XseB family.|||Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides.|||Cytoplasm|||Heterooligomer composed of large and small subunits. http://togogenome.org/gene/1863:CKV89_RS02560 ^@ http://purl.uniprot.org/uniprot/A0A239V9C9 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the UPF0410 family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS04440 ^@ http://purl.uniprot.org/uniprot/A0A239VEK2 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09330 ^@ http://purl.uniprot.org/uniprot/A0A239VQJ5 ^@ Similarity ^@ Belongs to the precorrin methyltransferase family. http://togogenome.org/gene/1863:CKV89_RS05765 ^@ http://purl.uniprot.org/uniprot/A0A239VG57 ^@ Similarity ^@ Belongs to the class-II fumarase/aspartase family. Aspartase subfamily. http://togogenome.org/gene/1863:CKV89_RS09935 ^@ http://purl.uniprot.org/uniprot/A0A239VQT0 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL16 family.|||Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs.|||Part of the 50S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS05670 ^@ http://purl.uniprot.org/uniprot/A0A239VHY6 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the FtsZ family.|||Cytoplasm|||Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity.|||Homodimer. Polymerizes to form a dynamic ring structure in a strictly GTP-dependent manner. Interacts directly with several other division proteins. http://togogenome.org/gene/1863:CKV89_RS10250 ^@ http://purl.uniprot.org/uniprot/A0A239VR93 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the complex I subunit 4L family.|||Cell membrane|||Membrane|||NDH-1 is composed of 14 different subunits. Subunits NuoA, H, J, K, L, M, N constitute the membrane sector of the complex.|||NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be a menaquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. http://togogenome.org/gene/1863:CKV89_RS01470 ^@ http://purl.uniprot.org/uniprot/A0A239V6K7 ^@ Activity Regulation|||Caution|||Function|||Similarity ^@ Allosterically activated by N-acetylglucosamine 6-phosphate (GlcNAc6P).|||Belongs to the glucosamine/galactosamine-6-phosphate isomerase family. NagB subfamily.|||Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS10225 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UEV2 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS01340 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YRT2 ^@ Caution|||Similarity|||Subcellular Location Annotation ^@ Belongs to the DedA family.|||Cell membrane|||Membrane|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS11155 ^@ http://purl.uniprot.org/uniprot/A0A239VU23 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the MotA family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS04775 ^@ http://purl.uniprot.org/uniprot/A0A239VDY0 ^@ Similarity ^@ Belongs to the glycosyl hydrolase 13 family. TreS subfamily. http://togogenome.org/gene/1863:CKV89_RS06895 ^@ http://purl.uniprot.org/uniprot/A0A239VJG6 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the NDK family.|||Cytoplasm|||Homotetramer.|||Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate. http://togogenome.org/gene/1863:CKV89_RS06145 ^@ http://purl.uniprot.org/uniprot/A0A239VIG2 ^@ Function|||Similarity|||Subunit ^@ Belongs to the RNA polymerase subunit omega family.|||Promotes RNA polymerase assembly. Latches the N- and C-terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits.|||The RNAP catalytic core consists of 2 alpha, 1 beta, 1 beta' and 1 omega subunit. When a sigma factor is associated with the core the holoenzyme is formed, which can initiate transcription. http://togogenome.org/gene/1863:CKV89_RS04100 ^@ http://purl.uniprot.org/uniprot/A0A239VCK6 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the cation transport ATPase (P-type) (TC 3.A.3) family. Type IA subfamily.|||Cell membrane|||Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit is responsible for energy coupling to the transport system and for the release of the potassium ions to the cytoplasm.|||The system is composed of three essential subunits: KdpA, KdpB and KdpC. http://togogenome.org/gene/1863:CKV89_RS07105 ^@ http://purl.uniprot.org/uniprot/A0A239VL05 ^@ Similarity ^@ Belongs to the FPG family. http://togogenome.org/gene/1863:CKV89_RS03940 ^@ http://purl.uniprot.org/uniprot/A0A239VCC0 ^@ Similarity ^@ In the N-terminal section; belongs to the cytochrome P450 family. http://togogenome.org/gene/1863:CKV89_RS11485 ^@ http://purl.uniprot.org/uniprot/A0A239VVD9 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the LemA family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS08295 ^@ http://purl.uniprot.org/uniprot/A0A239VMJ4 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the radical SAM superfamily. Biotin synthase family.|||Binds 1 [2Fe-2S] cluster. The cluster is coordinated with 3 cysteines and 1 arginine.|||Binds 1 [4Fe-4S] cluster. The cluster is coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine.|||Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical-based mechanism.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS08760 ^@ http://purl.uniprot.org/uniprot/A0A239VM81 ^@ Similarity ^@ Belongs to the glutamate synthase family. http://togogenome.org/gene/1863:CKV89_RS05155 ^@ http://purl.uniprot.org/uniprot/A0A239VF46 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the SMC family.|||Contains large globular domains required for ATP hydrolysis at each terminus and a third globular domain forming a flexible hinge near the middle of the molecule. These domains are separated by coiled-coil structures.|||Cytoplasm|||Homodimer.|||Required for chromosome condensation and partitioning. http://togogenome.org/gene/1863:CKV89_RS05005 ^@ http://purl.uniprot.org/uniprot/A0A239VEF8 ^@ Function ^@ Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second. http://togogenome.org/gene/1863:CKV89_RS04840 ^@ http://purl.uniprot.org/uniprot/A0A239VF28 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS08460 ^@ http://purl.uniprot.org/uniprot/A0A239VN80 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the radical SAM superfamily. MoaA family.|||Binds 2 [4Fe-4S] clusters. Binds 1 [4Fe-4S] cluster coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine and 1 [4Fe-4S] cluster coordinated with 3 cysteines and the GTP-derived substrate.|||Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8-dihydroguanosine 5'-triphosphate.|||Monomer and homodimer. http://togogenome.org/gene/1863:CKV89_RS02610 ^@ http://purl.uniprot.org/uniprot/A0A239VB25 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS04940 ^@ http://purl.uniprot.org/uniprot/A0A239VFL6 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS10860 ^@ http://purl.uniprot.org/uniprot/A0A239VU75 ^@ Similarity ^@ Belongs to the DegT/DnrJ/EryC1 family. http://togogenome.org/gene/1863:CKV89_RS08110 ^@ http://purl.uniprot.org/uniprot/A0A239VKR2 ^@ Similarity ^@ Belongs to the heat shock protein 70 family. http://togogenome.org/gene/1863:CKV89_RS07420 ^@ http://purl.uniprot.org/uniprot/A0A239VL37 ^@ Function|||Similarity ^@ Belongs to the RecO family.|||Involved in DNA repair and RecF pathway recombination. http://togogenome.org/gene/1863:CKV89_RS07365 ^@ http://purl.uniprot.org/uniprot/A0A239VJG5 ^@ Cofactor|||Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the DnaJ family.|||Binds 2 Zn(2+) ions per monomer.|||Cytoplasm|||Homodimer.|||Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins and by disaggregating proteins, also in an autonomous, DnaK-independent fashion. Unfolded proteins bind initially to DnaJ; upon interaction with the DnaJ-bound protein, DnaK hydrolyzes its bound ATP, resulting in the formation of a stable complex. GrpE releases ADP from DnaK; ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins.|||The J domain is necessary and sufficient to stimulate DnaK ATPase activity. Zinc center 1 plays an important role in the autonomous, DnaK-independent chaperone activity of DnaJ. Zinc center 2 is essential for interaction with DnaK and for DnaJ activity. http://togogenome.org/gene/1863:CKV89_RS08865 ^@ http://purl.uniprot.org/uniprot/A0A239VMR4 ^@ Similarity ^@ Belongs to the 2-oxoacid dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS11040 ^@ http://purl.uniprot.org/uniprot/A0A239VTZ6 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS07325 ^@ http://purl.uniprot.org/uniprot/A0A239VLB9 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the sigma-70 factor family. RpoD/SigA subfamily.|||Cytoplasm|||Interacts transiently with the RNA polymerase catalytic core.|||Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth. http://togogenome.org/gene/1863:CKV89_RS09960 ^@ http://purl.uniprot.org/uniprot/A0A239VRP8 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL23 family.|||One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome.|||Part of the 50S ribosomal subunit. Contacts protein L29, and trigger factor when it is bound to the ribosome. http://togogenome.org/gene/1863:CKV89_RS00570 ^@ http://purl.uniprot.org/uniprot/A0A239V439 ^@ Similarity ^@ Belongs to the PEP-utilizing enzyme family. http://togogenome.org/gene/1863:CKV89_RS02785 ^@ http://purl.uniprot.org/uniprot/A0A239V9U7 ^@ Similarity ^@ Belongs to the peptidase S13 family. http://togogenome.org/gene/1863:CKV89_RS04610 ^@ http://purl.uniprot.org/uniprot/A0A239VDK6 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the ATPase C chain family.|||Cell membrane|||F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation.|||Key component of the F(0) channel; it plays a direct role in translocation across the membrane. A homomeric c-ring of between 10-14 subunits forms the central stalk rotor element with the F(1) delta and epsilon subunits.|||Membrane http://togogenome.org/gene/1863:CKV89_RS06095 ^@ http://purl.uniprot.org/uniprot/A0A239VHZ2 ^@ Similarity ^@ Belongs to the aspartate/ornithine carbamoyltransferase superfamily. ATCase family. http://togogenome.org/gene/1863:CKV89_RS05610 ^@ http://purl.uniprot.org/uniprot/A0A239VHD8 ^@ Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the MraZ family.|||Forms oligomers.|||nucleoid http://togogenome.org/gene/1863:CKV89_RS02165 ^@ http://purl.uniprot.org/uniprot/A0A239VAC1 ^@ Similarity ^@ Belongs to the thioredoxin family. http://togogenome.org/gene/1863:CKV89_RS04575 ^@ http://purl.uniprot.org/uniprot/A0A239VF54 ^@ Function|||PTM|||Similarity|||Subcellular Location Annotation ^@ Belongs to the prokaryotic/mitochondrial release factor family.|||Cytoplasm|||Methylated by PrmC. Methylation increases the termination efficiency of RF1.|||Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA. http://togogenome.org/gene/1863:CKV89_RS05415 ^@ http://purl.uniprot.org/uniprot/A0A239VF10 ^@ Similarity ^@ Belongs to the carbamate kinase family. http://togogenome.org/gene/1863:CKV89_RS08650 ^@ http://purl.uniprot.org/uniprot/A0A239VNQ0 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the glyceraldehyde-3-phosphate dehydrogenase family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS09575 ^@ http://purl.uniprot.org/uniprot/A0A239VQK2 ^@ Function|||Similarity|||Subunit ^@ Belongs to the Mrp/NBP35 ATP-binding proteins family.|||Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS10205 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UCX1 ^@ Caution|||Cofactor|||Similarity|||Subcellular Location Annotation ^@ Belongs to the peptidase M48B family.|||Binds 1 zinc ion per subunit.|||Cell membrane|||Membrane|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS08635 ^@ http://purl.uniprot.org/uniprot/A0A239VLX5 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the SecG family.|||Cell membrane|||Involved in protein export. Participates in an early event of protein translocation.|||Membrane http://togogenome.org/gene/1863:CKV89_RS10300 ^@ http://purl.uniprot.org/uniprot/A0A239VT10 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the complex I subunit 3 family.|||Cell membrane|||NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. http://togogenome.org/gene/1863:CKV89_RS01505 ^@ http://purl.uniprot.org/uniprot/A0A239V6P7 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS06005 ^@ http://purl.uniprot.org/uniprot/A0A239VHT9 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the transglycosylase MltG family.|||Cell membrane|||Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation. http://togogenome.org/gene/1863:CKV89_RS05425 ^@ http://purl.uniprot.org/uniprot/A0A239VF21 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the arginine deiminase family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS10175 ^@ http://purl.uniprot.org/uniprot/A0A239VR20 ^@ Similarity ^@ Belongs to the bacterial ribosomal protein bL33 family. http://togogenome.org/gene/1863:CKV89_RS04550 ^@ http://purl.uniprot.org/uniprot/A0A239VDD9 ^@ Similarity ^@ Belongs to the homoserine dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS00985 ^@ http://purl.uniprot.org/uniprot/A0A239V5F4 ^@ Similarity ^@ Belongs to the zinc-containing alcohol dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS04975 ^@ http://purl.uniprot.org/uniprot/A0A239VFZ0 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-I aminoacyl-tRNA synthetase family. Glutamate--tRNA ligase type 1 subfamily.|||Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction: glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu).|||Cytoplasm|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Monomer. http://togogenome.org/gene/1863:CKV89_RS07390 ^@ http://purl.uniprot.org/uniprot/A0A239VJM7 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the endoribonuclease YbeY family.|||Binds 1 zinc ion.|||Cytoplasm|||Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA. http://togogenome.org/gene/1863:CKV89_RS08870 ^@ http://purl.uniprot.org/uniprot/A0A239VMK3 ^@ Function|||Miscellaneous|||Similarity|||Subcellular Location Annotation ^@ Belongs to the LipB family.|||Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate.|||Cytoplasm|||In the reaction, the free carboxyl group of octanoic acid is attached via an amide linkage to the epsilon-amino group of a specific lysine residue of lipoyl domains of lipoate-dependent enzymes. http://togogenome.org/gene/1863:CKV89_RS08940 ^@ http://purl.uniprot.org/uniprot/A0A239VPM4 ^@ Function|||Similarity ^@ Belongs to the aconitase/IPM isomerase family.|||Catalyzes the isomerization of citrate to isocitrate via cis-aconitate. http://togogenome.org/gene/1863:CKV89_RS10020 ^@ http://purl.uniprot.org/uniprot/A0A239VQG2 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL1 family.|||Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release.|||Part of the 50S ribosomal subunit.|||Protein L1 is also a translational repressor protein, it controls the translation of the L11 operon by binding to its mRNA. http://togogenome.org/gene/1863:CKV89_RS06805 ^@ http://purl.uniprot.org/uniprot/A0A239VK31 ^@ Similarity ^@ Belongs to the peptidase M1 family. http://togogenome.org/gene/1863:CKV89_RS01600 ^@ http://purl.uniprot.org/uniprot/A0A239V7A1 ^@ Function|||Miscellaneous|||Similarity|||Subcellular Location Annotation ^@ Bacitracin is thought to be involved in the inhibition of peptidoglycan synthesis by sequestering undecaprenyl diphosphate, thereby reducing the pool of lipid carrier available.|||Belongs to the UppP family.|||Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS10640 ^@ http://purl.uniprot.org/uniprot/A0A239VTW5 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the ribose-phosphate pyrophosphokinase family. Class I subfamily.|||Binds 2 Mg(2+) ions per subunit.|||Cytoplasm|||Homohexamer.|||Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P). http://togogenome.org/gene/1863:CKV89_RS03555 ^@ http://purl.uniprot.org/uniprot/A0A239VDK3 ^@ Caution|||Similarity|||Subcellular Location Annotation ^@ Belongs to the SURF1 family.|||Cell membrane|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS00260 ^@ http://purl.uniprot.org/uniprot/A0A239V3T3 ^@ Similarity ^@ Belongs to the glycosyl hydrolase 26 family. http://togogenome.org/gene/1863:CKV89_RS02215 ^@ http://purl.uniprot.org/uniprot/A0A239V8C9 ^@ Function|||Similarity ^@ Belongs to the bacterial ribosomal protein bS6 family.|||Binds together with bS18 to 16S ribosomal RNA. http://togogenome.org/gene/1863:CKV89_RS07120 ^@ http://purl.uniprot.org/uniprot/A0A239VJ74 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the 4-toluene sulfonate uptake permease (TSUP) (TC 2.A.102) family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS00320 ^@ http://purl.uniprot.org/uniprot/A0A239V4D2 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily.|||Membrane http://togogenome.org/gene/1863:CKV89_RS02810 ^@ http://purl.uniprot.org/uniprot/A0A239VB60 ^@ Subcellular Location Annotation ^@ Cytoplasm http://togogenome.org/gene/1863:CKV89_RS10740 ^@ http://purl.uniprot.org/uniprot/A0A239VUA8 ^@ Function|||Similarity|||Subunit ^@ Belongs to the MoaC family.|||Catalyzes the conversion of (8S)-3',8-cyclo-7,8-dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP).|||Homohexamer; trimer of dimers. http://togogenome.org/gene/1863:CKV89_RS01380 ^@ http://purl.uniprot.org/uniprot/A0A239V8T2 ^@ Similarity ^@ Belongs to the 5'-nucleotidase family. http://togogenome.org/gene/1863:CKV89_RS10230 ^@ http://purl.uniprot.org/uniprot/A0A239VSU2 ^@ Similarity ^@ Belongs to the FPP/GGPP synthase family. http://togogenome.org/gene/1863:CKV89_RS06710 ^@ http://purl.uniprot.org/uniprot/A0A239VJ47 ^@ Caution|||Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ A translation factor that gates the progression of the 70S ribosomal initiation complex (IC, containing tRNA(fMet) in the P-site) into the translation elongation cycle by using a mechanism sensitive to the ATP/ADP ratio. Binds to the 70S ribosome E-site where it modulates the state of the translating ribosome during subunit translocation. ATP hydrolysis probably frees it from the ribosome, which can enter the elongation phase.|||Belongs to the ABC transporter superfamily. ABCF family. Translational throttle EttA subfamily.|||Cytoplasm|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Monomer. Probably contacts ribosomal proteins L1, L5, L33 and S7, the 16S and 23S rRNA and the P-site containing tRNA(fMet).|||The P-site tRNA interaction motif (PtIM domain) probably interacts with the P-site tRNA(fMet) as well as the 23S rRNA.|||The arm domain is inserted in the first ABC transporter domain. Probably contacts ribosomal protein L1. http://togogenome.org/gene/1863:CKV89_RS09930 ^@ http://purl.uniprot.org/uniprot/A0A239VRY9 ^@ Similarity ^@ Belongs to the universal ribosomal protein uL29 family. http://togogenome.org/gene/1863:CKV89_RS09830 ^@ http://purl.uniprot.org/uniprot/A0A239VRB8 ^@ Similarity|||Subunit ^@ Belongs to the bacterial ribosomal protein bL17 family.|||Part of the 50S ribosomal subunit. Contacts protein L32. http://togogenome.org/gene/1863:CKV89_RS00410 ^@ http://purl.uniprot.org/uniprot/A0A239V591 ^@ Caution ^@ Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS10295 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UET5 ^@ Caution|||Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the complex I 20 kDa subunit family.|||Binds 1 [4Fe-4S] cluster.|||Cell membrane|||NDH-1 is composed of 14 different subunits. Subunits NuoB, C, D, E, F, and G constitute the peripheral sector of the complex.|||NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be a menaquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient.|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS05690 ^@ http://purl.uniprot.org/uniprot/A0A239VHK0 ^@ Similarity ^@ Belongs to the YggT family. http://togogenome.org/gene/1863:CKV89_RS09715 ^@ http://purl.uniprot.org/uniprot/A0A239VRI1 ^@ Similarity ^@ Belongs to the helicase family. RecQ subfamily. http://togogenome.org/gene/1863:CKV89_RS10035 ^@ http://purl.uniprot.org/uniprot/A0A239VSE9 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the SecE/SEC61-gamma family.|||Cell membrane|||Component of the Sec protein translocase complex. Heterotrimer consisting of SecY, SecE and SecG subunits. The heterotrimers can form oligomers, although 1 heterotrimer is thought to be able to translocate proteins. Interacts with the ribosome. Interacts with SecDF, and other proteins may be involved. Interacts with SecA.|||Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation. http://togogenome.org/gene/1863:CKV89_RS01895 ^@ http://purl.uniprot.org/uniprot/A0A239V907 ^@ Cofactor|||PTM|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family.|||Binds 2 nickel ions per subunit.|||Carbamylation allows a single lysine to coordinate two nickel ions.|||Carboxylation allows a single lysine to coordinate two nickel ions.|||Cytoplasm|||Heterotrimer of UreA (gamma), UreB (beta) and UreC (alpha) subunits. Three heterotrimers associate to form the active enzyme. http://togogenome.org/gene/1863:CKV89_RS09710 ^@ http://purl.uniprot.org/uniprot/A0A239VQW2 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09540 ^@ http://purl.uniprot.org/uniprot/A0A239VQD5 ^@ Cofactor|||Miscellaneous|||Similarity ^@ Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family.|||Binds 1 FAD per subunit.|||The active site is a redox-active disulfide bond. http://togogenome.org/gene/1863:CKV89_RS05335 ^@ http://purl.uniprot.org/uniprot/A0A239VF51 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the lactate permease family.|||Cell membrane|||Membrane|||Uptake of L-lactate across the membrane. Can also transport D-lactate and glycolate. http://togogenome.org/gene/1863:CKV89_RS08830 ^@ http://purl.uniprot.org/uniprot/A0A239VNL8 ^@ Function|||Similarity ^@ Belongs to the CobU/CobP family.|||Catalyzes ATP-dependent phosphorylation of adenosylcobinamide and addition of GMP to adenosylcobinamide phosphate. http://togogenome.org/gene/1863:CKV89_RS05445 ^@ http://purl.uniprot.org/uniprot/A0A239VGV1 ^@ Function|||Miscellaneous|||Similarity|||Subunit ^@ Belongs to the peroxiredoxin family. Tpx subfamily.|||Homodimer.|||The active site is a conserved redox-active cysteine residue, the peroxidatic cysteine (C(P)), which makes the nucleophilic attack on the peroxide substrate. The peroxide oxidizes the C(P)-SH to cysteine sulfenic acid (C(P)-SOH), which then reacts with another cysteine residue, the resolving cysteine (C(R)), to form a disulfide bridge. The disulfide is subsequently reduced by an appropriate electron donor to complete the catalytic cycle. In this atypical 2-Cys peroxiredoxin, C(R) is present in the same subunit to form an intramolecular disulfide. The disulfide is subsequently reduced by thioredoxin.|||Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides. http://togogenome.org/gene/1863:CKV89_RS07515 ^@ http://purl.uniprot.org/uniprot/A0A239VLL7 ^@ Function|||PTM|||Similarity|||Subcellular Location Annotation ^@ 4'-phosphopantetheine is transferred from CoA to a specific serine of apo-ACP by AcpS. This modification is essential for activity because fatty acids are bound in thioester linkage to the sulfhydryl of the prosthetic group.|||Belongs to the acyl carrier protein (ACP) family.|||Carrier of the growing fatty acid chain in fatty acid biosynthesis.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS09040 ^@ http://purl.uniprot.org/uniprot/A0A239VPY7 ^@ Similarity ^@ Belongs to the peptidase C40 family. http://togogenome.org/gene/1863:CKV89_RS06380 ^@ http://purl.uniprot.org/uniprot/A0A239VHY3 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the SecA family.|||Cell membrane|||Cytoplasm|||Monomer and homodimer. Part of the essential Sec protein translocation apparatus which comprises SecA, SecYEG and auxiliary proteins SecDF. Other proteins may also be involved.|||Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane. http://togogenome.org/gene/1863:CKV89_RS08780 ^@ http://purl.uniprot.org/uniprot/A0A239VMB1 ^@ Function|||Similarity|||Subunit ^@ Belongs to the TrpA family.|||Tetramer of two alpha and two beta chains.|||The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3-phosphate. http://togogenome.org/gene/1863:CKV89_RS06830 ^@ http://purl.uniprot.org/uniprot/A0A239VJL9 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the FKBP-type PPIase family. Tig subfamily.|||Consists of 3 domains; the N-terminus binds the ribosome, the middle domain has PPIase activity, while the C-terminus has intrinsic chaperone activity on its own.|||Cytoplasm|||Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase. http://togogenome.org/gene/1863:CKV89_RS02170 ^@ http://purl.uniprot.org/uniprot/A0A239V9J2 ^@ Cofactor|||Similarity|||Subunit ^@ Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family.|||Binds 1 FAD per subunit.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS08525 ^@ http://purl.uniprot.org/uniprot/A0A239VMU4 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS05705 ^@ http://purl.uniprot.org/uniprot/A0A239VG23 ^@ Function|||Similarity ^@ Belongs to the pseudouridine synthase RluA family.|||Responsible for synthesis of pseudouridine from uracil. http://togogenome.org/gene/1863:CKV89_RS03370 ^@ http://purl.uniprot.org/uniprot/A0A239VB72 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS08640 ^@ http://purl.uniprot.org/uniprot/A0A239VNV3 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the triosephosphate isomerase family.|||Cytoplasm|||Homodimer.|||Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P). http://togogenome.org/gene/1863:CKV89_RS10000 ^@ http://purl.uniprot.org/uniprot/A0A239VQD8 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the RNA polymerase beta' chain family.|||Binds 1 Mg(2+) ion per subunit.|||Binds 2 Zn(2+) ions per subunit.|||DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates.|||The RNAP catalytic core consists of 2 alpha, 1 beta, 1 beta' and 1 omega subunit. When a sigma factor is associated with the core the holoenzyme is formed, which can initiate transcription. http://togogenome.org/gene/1863:CKV89_RS03840 ^@ http://purl.uniprot.org/uniprot/A0A239VDJ6 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS05800 ^@ http://purl.uniprot.org/uniprot/A0A239VHT8 ^@ Cofactor|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily.|||Binds 2 magnesium ions per tetramer.|||Cytoplasm|||Tetramer of two alpha and two beta subunits. http://togogenome.org/gene/1863:CKV89_RS10715 ^@ http://purl.uniprot.org/uniprot/A0A239VU43 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the methyltransferase superfamily. RsmI family.|||Belongs to the precorrin methyltransferase family.|||Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS10635 ^@ http://purl.uniprot.org/uniprot/A0A239VUA2 ^@ Function|||Similarity|||Subunit ^@ Belongs to the bacterial ribosomal protein bL25 family. CTC subfamily.|||Part of the 50S ribosomal subunit; part of the 5S rRNA/L5/L18/L25 subcomplex. Contacts the 5S rRNA. Binds to the 5S rRNA independently of L5 and L18.|||This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance. http://togogenome.org/gene/1863:CKV89_RS02060 ^@ http://purl.uniprot.org/uniprot/A0A239V8A9 ^@ Function|||Similarity ^@ Belongs to the cyclophilin-type PPIase family.|||PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. http://togogenome.org/gene/1863:CKV89_RS10365 ^@ http://purl.uniprot.org/uniprot/A0A239VRL6 ^@ Function|||Subcellular Location Annotation|||Subunit ^@ Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source.|||Cytoplasm|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS01865 ^@ http://purl.uniprot.org/uniprot/A0A239V7W1 ^@ Similarity ^@ Belongs to the 4-hydroxybenzoyl-CoA thioesterase family. http://togogenome.org/gene/1863:CKV89_RS06050 ^@ http://purl.uniprot.org/uniprot/A0A239VHP9 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the acetokinase family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS08270 ^@ http://purl.uniprot.org/uniprot/A0A239VMH5 ^@ Similarity|||Subunit ^@ Belongs to the AAA ATPase family.|||Homohexamer. Assembles into a hexameric ring structure. http://togogenome.org/gene/1863:CKV89_RS07215 ^@ http://purl.uniprot.org/uniprot/A0A239VKN5 ^@ Function|||Similarity|||Subunit ^@ Belongs to the peptidase S24 family.|||Homodimer.|||Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair. http://togogenome.org/gene/1863:CKV89_RS04340 ^@ http://purl.uniprot.org/uniprot/A0A239VD55 ^@ Function|||Similarity ^@ Belongs to the trehalose phosphatase family.|||Removes the phosphate from trehalose 6-phosphate to produce free trehalose. http://togogenome.org/gene/1863:CKV89_RS03325 ^@ http://purl.uniprot.org/uniprot/A0A239VB00 ^@ Similarity|||Subunit ^@ Belongs to the ALAD family.|||Homooctamer. http://togogenome.org/gene/1863:CKV89_RS01585 ^@ http://purl.uniprot.org/uniprot/A0A239V8B9 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS10135 ^@ http://purl.uniprot.org/uniprot/A0A239VSP0 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS00880 ^@ http://purl.uniprot.org/uniprot/A0A239V559 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the selenophosphate synthase 1 family. Class I subfamily.|||Binds 1 Mg(2+) ion per monomer.|||Homodimer.|||Synthesizes selenophosphate from selenide and ATP. http://togogenome.org/gene/1863:CKV89_RS09590 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YRB2 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS10405 ^@ http://purl.uniprot.org/uniprot/A0A239VSZ3 ^@ Function|||Similarity ^@ Belongs to the MsrA Met sulfoxide reductase family.|||Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine. http://togogenome.org/gene/1863:CKV89_RS08580 ^@ http://purl.uniprot.org/uniprot/A0A239VNS0 ^@ Similarity ^@ Belongs to the UPF0051 (ycf24) family. http://togogenome.org/gene/1863:CKV89_RS01915 ^@ http://purl.uniprot.org/uniprot/A0A239V7Q0 ^@ Similarity ^@ Belongs to the FPG family. http://togogenome.org/gene/1863:CKV89_RS03300 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YQ84 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS00805 ^@ http://purl.uniprot.org/uniprot/A0A239V5R2 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-II aminoacyl-tRNA synthetase family. Type-1 seryl-tRNA synthetase subfamily.|||Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec).|||Consists of two distinct domains, a catalytic core and a N-terminal extension that is involved in tRNA binding.|||Cytoplasm|||Homodimer. The tRNA molecule binds across the dimer. http://togogenome.org/gene/1863:CKV89_RS10690 ^@ http://purl.uniprot.org/uniprot/A0A239VU11 ^@ Caution|||Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-I aminoacyl-tRNA synthetase family. MetG type 1 subfamily.|||Binds 1 zinc ion per subunit.|||Cytoplasm|||Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Monomer. http://togogenome.org/gene/1863:CKV89_RS03025 ^@ http://purl.uniprot.org/uniprot/A0A239VAU1 ^@ Function|||Similarity ^@ Belongs to the glutaredoxin family.|||Electron transport system for the ribonucleotide reductase system NrdEF. http://togogenome.org/gene/1863:CKV89_RS05355 ^@ http://purl.uniprot.org/uniprot/A0A239VF69 ^@ Caution|||Function|||Similarity ^@ Belongs to the DXR family.|||Catalyzes the NADPH-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP).|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS00395 ^@ http://purl.uniprot.org/uniprot/A0A239V5T5 ^@ Similarity ^@ Belongs to the 5-formyltetrahydrofolate cyclo-ligase family. http://togogenome.org/gene/1863:CKV89_RS03640 ^@ http://purl.uniprot.org/uniprot/A0A239VD53 ^@ Caution|||Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the succinate/malate CoA ligase beta subunit family.|||Binds 1 Mg(2+) ion per subunit.|||Heterotetramer of two alpha and two beta subunits.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit. http://togogenome.org/gene/1863:CKV89_RS03350 ^@ http://purl.uniprot.org/uniprot/A0A239VB62 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09670 ^@ http://purl.uniprot.org/uniprot/A0A239VRD0 ^@ Similarity ^@ Belongs to the Nudix hydrolase family. http://togogenome.org/gene/1863:CKV89_RS02235 ^@ http://purl.uniprot.org/uniprot/A0A239V9M7 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS07400 ^@ http://purl.uniprot.org/uniprot/A0A239VJI7 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism.|||Belongs to the TRAFAC class TrmE-Era-EngA-EngB-Septin-like GTPase superfamily. Era GTPase family.|||Cell membrane|||Cytoplasm|||Monomer. http://togogenome.org/gene/1863:CKV89_RS05555 ^@ http://purl.uniprot.org/uniprot/A0A239VGF8 ^@ Function|||Similarity|||Subunit ^@ Belongs to the bacterial ribosomal protein bL21 family.|||Part of the 50S ribosomal subunit. Contacts protein L20.|||This protein binds to 23S rRNA in the presence of protein L20. http://togogenome.org/gene/1863:CKV89_RS09255 ^@ http://purl.uniprot.org/uniprot/A0A239VNJ4 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the heme-copper respiratory oxidase family.|||Cell membrane|||Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B.|||Membrane http://togogenome.org/gene/1863:CKV89_RS00730 ^@ http://purl.uniprot.org/uniprot/A0A239V5J0 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the cytochrome ubiquinol oxidase subunit 2 family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS08100 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YSW5 ^@ Caution|||Similarity ^@ Belongs to the N-acetylmuramoyl-L-alanine amidase 2 family.|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS11220 ^@ http://purl.uniprot.org/uniprot/A0A239VVM5 ^@ Similarity|||Subcellular Location Annotation ^@ Bacterial flagellum basal body|||Belongs to the FliE family. http://togogenome.org/gene/1863:CKV89_RS03035 ^@ http://purl.uniprot.org/uniprot/A0A239VAC0 ^@ Function|||Similarity ^@ Belongs to the ribonucleoside diphosphate reductase large chain family.|||Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides. http://togogenome.org/gene/1863:CKV89_RS09325 ^@ http://purl.uniprot.org/uniprot/A0A239VQM6 ^@ Similarity ^@ Belongs to the precorrin methyltransferase family. http://togogenome.org/gene/1863:CKV89_RS02285 ^@ http://purl.uniprot.org/uniprot/A0A239V964 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09910 ^@ http://purl.uniprot.org/uniprot/A0A239VRK0 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL5 family.|||Part of the 50S ribosomal subunit; part of the 5S rRNA/L5/L18/L25 subcomplex. Contacts the 5S rRNA and the P site tRNA. Forms a bridge to the 30S subunit in the 70S ribosome.|||This is 1 of the proteins that bind and probably mediate the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits; this bridge is implicated in subunit movement. Contacts the P site tRNA; the 5S rRNA and some of its associated proteins might help stabilize positioning of ribosome-bound tRNAs. http://togogenome.org/gene/1863:CKV89_RS06845 ^@ http://purl.uniprot.org/uniprot/A0A239VK52 ^@ Function|||Similarity|||Subunit ^@ ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP.|||Belongs to the ClpX chaperone family.|||Component of the ClpX-ClpP complex. Forms a hexameric ring that, in the presence of ATP, binds to fourteen ClpP subunits assembled into a disk-like structure with a central cavity, resembling the structure of eukaryotic proteasomes. http://togogenome.org/gene/1863:CKV89_RS08625 ^@ http://purl.uniprot.org/uniprot/A0A239VNN2 ^@ Caution|||Function|||Similarity ^@ Belongs to the glucose-6-phosphate dehydrogenase family.|||Catalyzes the oxidation of glucose 6-phosphate to 6-phosphogluconolactone.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS08095 ^@ http://purl.uniprot.org/uniprot/A0A239VLD7 ^@ Activity Regulation|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the phosphofructokinase type A (PFKA) family. PPi-dependent PFK group II subfamily. Clade 'P' sub-subfamily.|||Catalyzes the phosphorylation of D-fructose 6-phosphate, the first committing step of glycolysis. Uses inorganic phosphate (PPi) as phosphoryl donor instead of ATP like common ATP-dependent phosphofructokinases (ATP-PFKs), which renders the reaction reversible, and can thus function both in glycolysis and gluconeogenesis. Consistently, PPi-PFK can replace the enzymes of both the forward (ATP-PFK) and reverse (fructose-bisphosphatase (FBPase)) reactions.|||Cytoplasm|||Homodimer or homotetramer.|||Non-allosteric. http://togogenome.org/gene/1863:CKV89_RS05105 ^@ http://purl.uniprot.org/uniprot/A0A239VFQ3 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the bacterial CoaD family.|||Cytoplasm|||Homohexamer.|||Reversibly transfers an adenylyl group from ATP to 4'-phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate. http://togogenome.org/gene/1863:CKV89_RS07595 ^@ http://purl.uniprot.org/uniprot/A0A239VJT3 ^@ Function|||Similarity ^@ Belongs to the carbohydrate kinase PfkB family.|||Catalyzes the ATP-dependent phosphorylation of fructose-l-phosphate to fructose-l,6-bisphosphate. http://togogenome.org/gene/1863:CKV89_RS09850 ^@ http://purl.uniprot.org/uniprot/A0A239VR85 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS13 family.|||Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits; these bridges are implicated in subunit movement. Contacts the tRNAs in the A and P-sites.|||Part of the 30S ribosomal subunit. Forms a loose heterodimer with protein S19. Forms two bridges to the 50S subunit in the 70S ribosome. http://togogenome.org/gene/1863:CKV89_RS10460 ^@ http://purl.uniprot.org/uniprot/A0A239VTS3 ^@ Activity Regulation|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the enolase family.|||Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis.|||Cell surface|||Cytoplasm|||Secreted|||The covalent binding to the substrate causes inactivation of the enzyme, and possibly serves as a signal for the export of the protein. http://togogenome.org/gene/1863:CKV89_RS07540 ^@ http://purl.uniprot.org/uniprot/A0A239VLH2 ^@ Function ^@ Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). http://togogenome.org/gene/1863:CKV89_RS04990 ^@ http://purl.uniprot.org/uniprot/A0A239VG01 ^@ Similarity ^@ Belongs to the class-I aminoacyl-tRNA synthetase family. http://togogenome.org/gene/1863:CKV89_RS05420 ^@ http://purl.uniprot.org/uniprot/A0A239VFE5 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the aspartate/ornithine carbamoyltransferase superfamily. OTCase family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS08445 ^@ http://purl.uniprot.org/uniprot/A0A239VNE1 ^@ Similarity ^@ Belongs to the short-chain dehydrogenases/reductases (SDR) family. FabI subfamily. http://togogenome.org/gene/1863:CKV89_RS05560 ^@ http://purl.uniprot.org/uniprot/A0A239VG07 ^@ Similarity ^@ Belongs to the bacterial ribosomal protein bL27 family. http://togogenome.org/gene/1863:CKV89_RS05995 ^@ http://purl.uniprot.org/uniprot/A0A239VGN6 ^@ Cofactor|||Domain|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the class-II aminoacyl-tRNA synthetase family.|||Binds 1 zinc ion per subunit.|||Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction: alanine is first activated by ATP to form Ala-AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain.|||Consists of three domains; the N-terminal catalytic domain, the editing domain and the C-terminal C-Ala domain. The editing domain removes incorrectly charged amino acids, while the C-Ala domain, along with tRNA(Ala), serves as a bridge to cooperatively bring together the editing and aminoacylation centers thus stimulating deacylation of misacylated tRNAs.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS07765 ^@ http://purl.uniprot.org/uniprot/A0A239VK43 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the transketolase family. DXPS subfamily.|||Binds 1 Mg(2+) ion per subunit.|||Binds 1 thiamine pyrophosphate per subunit.|||Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP).|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS03315 ^@ http://purl.uniprot.org/uniprot/A0A239VAY8 ^@ Cofactor|||Function|||Miscellaneous|||Similarity|||Subunit ^@ Belongs to the HMBS family.|||Binds 1 dipyrromethane group covalently.|||Monomer.|||Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps.|||The porphobilinogen subunits are added to the dipyrromethane group. http://togogenome.org/gene/1863:CKV89_RS00215 ^@ http://purl.uniprot.org/uniprot/A0A239V309 ^@ Similarity ^@ Belongs to the UPF0246 family. http://togogenome.org/gene/1863:CKV89_RS04760 ^@ http://purl.uniprot.org/uniprot/A0A239VEN4 ^@ Similarity ^@ Belongs to the phosphohexose mutase family. http://togogenome.org/gene/1863:CKV89_RS07340 ^@ http://purl.uniprot.org/uniprot/A0A239VJM0 ^@ Caution|||Function|||Similarity ^@ Belongs to the class I-like SAM-binding methyltransferase superfamily. TrmB family.|||Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS05855 ^@ http://purl.uniprot.org/uniprot/A0A239VGS4 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the NAD kinase family.|||Cytoplasm|||Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS08565 ^@ http://purl.uniprot.org/uniprot/A0A239VM09 ^@ Similarity ^@ Belongs to the ABC transporter superfamily. Ycf16 family. http://togogenome.org/gene/1863:CKV89_RS04415 ^@ http://purl.uniprot.org/uniprot/A0A239VEH1 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the uracil-DNA glycosylase (UDG) superfamily. UNG family.|||Cytoplasm|||Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine. http://togogenome.org/gene/1863:CKV89_RS10095 ^@ http://purl.uniprot.org/uniprot/A0A239VQP5 ^@ Function ^@ The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane. http://togogenome.org/gene/1863:CKV89_RS07945 ^@ http://purl.uniprot.org/uniprot/A0A239VLI5 ^@ Function|||Similarity|||Subunit ^@ Belongs to the glutaminase PdxT/SNO family.|||Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS.|||In the presence of PdxS, forms a dodecamer of heterodimers. Only shows activity in the heterodimer. http://togogenome.org/gene/1863:CKV89_RS07615 ^@ http://purl.uniprot.org/uniprot/A0A239VJX6 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS08710 ^@ http://purl.uniprot.org/uniprot/A0A239VN89 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the CoaE family.|||Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A.|||Cytoplasm|||In the C-terminal section; belongs to the UPF0157 (GrpB) family.|||In the N-terminal section; belongs to the CoaE family. http://togogenome.org/gene/1863:CKV89_RS02025 ^@ http://purl.uniprot.org/uniprot/A0A239V7X8 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS07520 ^@ http://purl.uniprot.org/uniprot/A0A239VJP3 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the thiolase-like superfamily. FabH family.|||Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched-chain and/or straight-chain of fatty acids.|||Cytoplasm|||Homodimer.|||The last Arg residue of the ACP-binding site is essential for the weak association between ACP/AcpP and FabH. http://togogenome.org/gene/1863:CKV89_RS06100 ^@ http://purl.uniprot.org/uniprot/A0A239VID7 ^@ Caution|||Cofactor|||Function|||Similarity ^@ Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily.|||Binds 2 Zn(2+) ions per subunit.|||Catalyzes the reversible cyclization of carbamoyl aspartate to dihydroorotate.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS04470 ^@ http://purl.uniprot.org/uniprot/A0A239VD69 ^@ Similarity ^@ Belongs to the peptidase M13 family. http://togogenome.org/gene/1863:CKV89_RS00755 ^@ http://purl.uniprot.org/uniprot/A0A239V684 ^@ Function ^@ Catalyzes two reactions in de novo purine nucleotide biosynthesis. Catalyzes the breakdown of 5-aminoimidazole- (N-succinylocarboxamide) ribotide (SAICAR or 2-[5-amino-1-(5-phospho-beta-D-ribosyl)imidazole-4-carboxamido]succinate) to 5-aminoimidazole-4-carboxamide ribotide (AICAR or 5-amino-1-(5-phospho-beta-D-ribosyl)imidazole-4-carboxamide) and fumarate, and of adenylosuccinate (ADS or N(6)-(1,2-dicarboxyethyl)-AMP) to adenosine monophosphate (AMP) and fumarate. http://togogenome.org/gene/1863:CKV89_RS03205 ^@ http://purl.uniprot.org/uniprot/A0A239VB77 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the purine/pyrimidine phosphoribosyltransferase family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS07705 ^@ http://purl.uniprot.org/uniprot/A0A239VLV1 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS00830 ^@ http://purl.uniprot.org/uniprot/A0A239V6F0 ^@ Similarity ^@ Belongs to the methyl-accepting chemotaxis (MCP) protein family. http://togogenome.org/gene/1863:CKV89_RS04275 ^@ http://purl.uniprot.org/uniprot/A0A239VCZ5 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the PhoU family.|||Cytoplasm|||Homodimer.|||Plays a role in the regulation of phosphate uptake. http://togogenome.org/gene/1863:CKV89_RS09970 ^@ http://purl.uniprot.org/uniprot/A0A239VRN0 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL3 family.|||One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit.|||Part of the 50S ribosomal subunit. Forms a cluster with proteins L14 and L19. http://togogenome.org/gene/1863:CKV89_RS03460 ^@ http://purl.uniprot.org/uniprot/A0A239VDF5 ^@ Activity Regulation|||Caution|||Function|||Similarity|||Subunit ^@ Belongs to the IMPDH/GMPR family.|||Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate-limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth.|||Homotetramer.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Mycophenolic acid (MPA) is a non-competitive inhibitor that prevents formation of the closed enzyme conformation by binding to the same site as the amobile flap. In contrast, mizoribine monophosphate (MZP) is a competitive inhibitor that induces the closed conformation. MPA is a potent inhibitor of mammalian IMPDHs but a poor inhibitor of the bacterial enzymes. MZP is a more potent inhibitor of bacterial IMPDH. http://togogenome.org/gene/1863:CKV89_RS09505 ^@ http://purl.uniprot.org/uniprot/A0A239VQW5 ^@ Similarity ^@ Belongs to the helicase family. UvrD subfamily. http://togogenome.org/gene/1863:CKV89_RS12510 ^@ http://purl.uniprot.org/uniprot/A0A239VDS9 ^@ Similarity ^@ Belongs to the transglycosylase family. Rpf subfamily. http://togogenome.org/gene/1863:CKV89_RS08645 ^@ http://purl.uniprot.org/uniprot/A0A239VNX2 ^@ Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the phosphoglycerate kinase family.|||Cytoplasm|||Monomer. http://togogenome.org/gene/1863:CKV89_RS07060 ^@ http://purl.uniprot.org/uniprot/A0A239VJ48 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and/or decay.|||Belongs to the metallo-beta-lactamase superfamily. RNA-metabolizing metallo-beta-lactamase-like family. Bacterial RNase J subfamily.|||Cytoplasm|||Homodimer, may be a subunit of the RNA degradosome. http://togogenome.org/gene/1863:CKV89_RS08185 ^@ http://purl.uniprot.org/uniprot/A0A239VM24 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the RNA polymerase-binding protein RbpA family.|||Bind 1 Zn(2+) per subunit.|||Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters.|||Forms a complex with the RNAP catalytic core and with free principal sigma factors. http://togogenome.org/gene/1863:CKV89_RS12420 ^@ http://purl.uniprot.org/uniprot/A0A239V5D5 ^@ Similarity ^@ Belongs to the CbxX/CfxQ family. http://togogenome.org/gene/1863:CKV89_RS07370 ^@ http://purl.uniprot.org/uniprot/A0A239VL07 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the RNA methyltransferase RsmE family.|||Cytoplasm|||Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS09380 ^@ http://purl.uniprot.org/uniprot/A0A239VQ59 ^@ Function|||Similarity ^@ Belongs to the threonine synthase family.|||Catalyzes the gamma-elimination of phosphate from L-phosphohomoserine and the beta-addition of water to produce L-threonine. http://togogenome.org/gene/1863:CKV89_RS09890 ^@ http://purl.uniprot.org/uniprot/A0A239VRR3 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL18 family.|||Part of the 50S ribosomal subunit; part of the 5S rRNA/L5/L18/L25 subcomplex. Contacts the 5S and 23S rRNAs.|||This is one of the proteins that bind and probably mediate the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. http://togogenome.org/gene/1863:CKV89_RS06155 ^@ http://purl.uniprot.org/uniprot/A0A239VIG5 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the AdoMet synthase family.|||Binds 1 potassium ion per subunit.|||Binds 2 divalent ions per subunit.|||Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme.|||Cytoplasm|||Homotetramer; dimer of dimers. http://togogenome.org/gene/1863:CKV89_RS05215 ^@ http://purl.uniprot.org/uniprot/A0A239VEK4 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes.|||Belongs to the RimM family.|||Binds ribosomal protein uS19.|||Cytoplasm|||The PRC barrel domain binds ribosomal protein uS19. http://togogenome.org/gene/1863:CKV89_RS08840 ^@ http://purl.uniprot.org/uniprot/A0A239VMH7 ^@ Similarity ^@ Belongs to the GcvT family. http://togogenome.org/gene/1863:CKV89_RS11215 ^@ http://purl.uniprot.org/uniprot/A0A239VU45 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Bacterial flagellum basal body|||Belongs to the FliF family.|||Membrane|||The M ring may be actively involved in energy transduction. http://togogenome.org/gene/1863:CKV89_RS07445 ^@ http://purl.uniprot.org/uniprot/A0A239VKQ8 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the acetokinase family.|||Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction.|||Cytoplasm|||Homodimer.|||Mg(2+). Can also accept Mn(2+). http://togogenome.org/gene/1863:CKV89_RS06065 ^@ http://purl.uniprot.org/uniprot/A0A239VII9 ^@ Similarity ^@ Belongs to the 2-oxoacid dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS06140 ^@ http://purl.uniprot.org/uniprot/A0A239VGW8 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the guanylate kinase family.|||Cytoplasm|||Essential for recycling GMP and indirectly, cGMP. http://togogenome.org/gene/1863:CKV89_RS04590 ^@ http://purl.uniprot.org/uniprot/A0A239VDI8 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS01150 ^@ http://purl.uniprot.org/uniprot/A0A239V5P4 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the ABC-3 integral membrane protein family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS09860 ^@ http://purl.uniprot.org/uniprot/A0A239VQ02 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the peptidase M24A family. Methionine aminopeptidase type 1 subfamily.|||Binds 2 divalent metal cations per subunit. Has a high-affinity and a low affinity metal-binding site. The true nature of the physiological cofactor is under debate. The enzyme is active with cobalt, zinc, manganese or divalent iron ions. Most likely, methionine aminopeptidases function as mononuclear Fe(2+)-metalloproteases under physiological conditions, and the catalytically relevant metal-binding site has been assigned to the histidine-containing high-affinity site.|||Monomer.|||Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed. http://togogenome.org/gene/1863:CKV89_RS07610 ^@ http://purl.uniprot.org/uniprot/A0A239VLA3 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS00090 ^@ http://purl.uniprot.org/uniprot/A0A239V3J1 ^@ Function ^@ Electron transfer subunit of the terminal reductase during anaerobic growth on various sulfoxide and N-oxide compounds. http://togogenome.org/gene/1863:CKV89_RS07345 ^@ http://purl.uniprot.org/uniprot/A0A239VKX1 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the anaerobic coproporphyrinogen-III oxidase family. HemW subfamily.|||Cytoplasm|||Probably acts as a heme chaperone, transferring heme to an unknown acceptor. Binds one molecule of heme per monomer, possibly covalently. Binds 1 [4Fe-4S] cluster. The cluster is coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine. http://togogenome.org/gene/1863:CKV89_RS08410 ^@ http://purl.uniprot.org/uniprot/A0A239VND7 ^@ Similarity ^@ Belongs to the band 7/mec-2 family. http://togogenome.org/gene/1863:CKV89_RS01910 ^@ http://purl.uniprot.org/uniprot/A0A239V7M7 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the alanine or glycine:cation symporter (AGCS) (TC 2.A.25) family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS09805 ^@ http://purl.uniprot.org/uniprot/A0A239VRM1 ^@ Cofactor|||Function|||PTM|||Similarity ^@ Activated by phosphorylation.|||Belongs to the phosphohexose mutase family.|||Binds 1 Mg(2+) ion per subunit.|||Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate. http://togogenome.org/gene/1863:CKV89_RS05850 ^@ http://purl.uniprot.org/uniprot/A0A239VHY5 ^@ Similarity ^@ Belongs to the TlyA family. http://togogenome.org/gene/1863:CKV89_RS08025 ^@ http://purl.uniprot.org/uniprot/A0A239VL81 ^@ Similarity ^@ Belongs to the pseudouridine synthase RsuA family. http://togogenome.org/gene/1863:CKV89_RS04345 ^@ http://purl.uniprot.org/uniprot/A0A239VD43 ^@ Similarity ^@ Belongs to the glycosyltransferase 20 family. http://togogenome.org/gene/1863:CKV89_RS01475 ^@ http://purl.uniprot.org/uniprot/A0A239V812 ^@ Cofactor|||Similarity ^@ Belongs to the metallo-dependent hydrolases superfamily. NagA family.|||Binds 1 divalent metal cation per subunit. http://togogenome.org/gene/1863:CKV89_RS02120 ^@ http://purl.uniprot.org/uniprot/A0A239V841 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the DnaA family.|||Cytoplasm|||Plays an important role in the initiation and regulation of chromosomal replication. Binds to the origin of replication; it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box): 5'-TTATC[CA]A[CA]A-3'. DnaA binds to ATP and to acidic phospholipids. http://togogenome.org/gene/1863:CKV89_RS07265 ^@ http://purl.uniprot.org/uniprot/A0A239VJA3 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family.|||Cell membrane http://togogenome.org/gene/1863:CKV89_RS08475 ^@ http://purl.uniprot.org/uniprot/A0A239VMP7 ^@ Function|||Miscellaneous|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-II fumarase/aspartase family. Fumarase subfamily.|||Cytoplasm|||Homotetramer.|||Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate.|||There are 2 substrate-binding sites: the catalytic A site, and the non-catalytic B site that may play a role in the transfer of substrate or product between the active site and the solvent. Alternatively, the B site may bind allosteric effectors. http://togogenome.org/gene/1863:CKV89_RS09945 ^@ http://purl.uniprot.org/uniprot/A0A239VQB3 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL22 family.|||Part of the 50S ribosomal subunit.|||The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome.|||This protein binds specifically to 23S rRNA; its binding is stimulated by other ribosomal proteins, e.g., L4, L17, and L20. It is important during the early stages of 50S assembly. It makes multiple contacts with different domains of the 23S rRNA in the assembled 50S subunit and ribosome. http://togogenome.org/gene/1863:CKV89_RS12410 ^@ http://purl.uniprot.org/uniprot/A0A239V392 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09025 ^@ http://purl.uniprot.org/uniprot/A0A239VNN5 ^@ Similarity ^@ Belongs to the type II topoisomerase GyrA/ParC subunit family. http://togogenome.org/gene/1863:CKV89_RS11240 ^@ http://purl.uniprot.org/uniprot/A0A239VVS8 ^@ Domain|||Function|||PTM|||Similarity|||Subcellular Location Annotation ^@ Belongs to the CheB family.|||Contains a C-terminal catalytic domain, and an N-terminal region which modulates catalytic activity.|||Cytoplasm|||Involved in chemotaxis. Part of a chemotaxis signal transduction system that modulates chemotaxis in response to various stimuli. Catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins or MCP) by CheR. Also mediates the irreversible deamidation of specific glutamine residues to glutamic acid.|||Phosphorylated by CheA. Phosphorylation of the N-terminal regulatory domain activates the methylesterase activity. http://togogenome.org/gene/1863:CKV89_RS07150 ^@ http://purl.uniprot.org/uniprot/A0A239VJJ4 ^@ Caution|||Function|||Similarity|||Subunit ^@ Belongs to the IPP transferase family.|||Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A).|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Monomer. http://togogenome.org/gene/1863:CKV89_RS04250 ^@ http://purl.uniprot.org/uniprot/A0A239VDH8 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ A Gly-cisPro motif from one monomer fits into the active site of the other monomer to allow specific chiral rejection of L-amino acids.|||An aminoacyl-tRNA editing enzyme that deacylates mischarged D-aminoacyl-tRNAs. Also deacylates mischarged glycyl-tRNA(Ala), protecting cells against glycine mischarging by AlaRS. Acts via tRNA-based rather than protein-based catalysis; rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality.|||Belongs to the DTD family.|||Cytoplasm|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS07795 ^@ http://purl.uniprot.org/uniprot/A0A239VKC3 ^@ Cofactor|||Function|||Similarity ^@ Belongs to the ChdC family. Type 2 subfamily.|||Fe-coproporphyrin III acts as both substrate and redox cofactor.|||Involved in coproporphyrin-dependent heme b biosynthesis. Catalyzes the decarboxylation of Fe-coproporphyrin III (coproheme) to heme b (protoheme IX), the last step of the pathway. The reaction occurs in a stepwise manner with a three-propionate intermediate. http://togogenome.org/gene/1863:CKV89_RS02015 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UEH6 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS08505 ^@ http://purl.uniprot.org/uniprot/A0A239VMB2 ^@ Cofactor|||Function|||Similarity ^@ Belongs to the TPP enzyme family.|||Binds 1 Mg(2+) per subunit.|||Decarboxylates branched-chain and aromatic alpha-keto acids to aldehydes. http://togogenome.org/gene/1863:CKV89_RS02820 ^@ http://purl.uniprot.org/uniprot/A0A239VBZ5 ^@ Similarity ^@ Belongs to the LytR/CpsA/Psr (LCP) family. http://togogenome.org/gene/1863:CKV89_RS01835 ^@ http://purl.uniprot.org/uniprot/A0A239V998 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation ^@ Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine.|||Belongs to the organic radical-activating enzymes family.|||Binds 1 [4Fe-4S] cluster. The cluster is coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS05375 ^@ http://purl.uniprot.org/uniprot/A0A239VFA7 ^@ Cofactor|||Function|||Similarity ^@ Belongs to the IspG family.|||Binds 1 [4Fe-4S] cluster.|||Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate. http://togogenome.org/gene/1863:CKV89_RS11165 ^@ http://purl.uniprot.org/uniprot/A0A239VVB5 ^@ Similarity ^@ Belongs to the flagella basal body rod proteins family. http://togogenome.org/gene/1863:CKV89_RS00240 ^@ http://purl.uniprot.org/uniprot/A0A239V379 ^@ Similarity ^@ Belongs to the UDP-glucose/GDP-mannose dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS07935 ^@ http://purl.uniprot.org/uniprot/A0A239VLH6 ^@ Function|||Similarity|||Subunit ^@ Belongs to the PdxS/SNZ family.|||Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively.|||In the presence of PdxT, forms a dodecamer of heterodimers. http://togogenome.org/gene/1863:CKV89_RS08670 ^@ http://purl.uniprot.org/uniprot/A0A239VNZ6 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the UvrC family.|||Cytoplasm|||Interacts with UvrB in an incision complex.|||The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision. http://togogenome.org/gene/1863:CKV89_RS01420 ^@ http://purl.uniprot.org/uniprot/A0A239V7W4 ^@ Similarity ^@ Belongs to the FKBP-type PPIase family. http://togogenome.org/gene/1863:CKV89_RS07230 ^@ http://purl.uniprot.org/uniprot/A0A239VL83 ^@ Function|||Similarity ^@ Belongs to the ribonucleoside diphosphate reductase class-2 family.|||Catalyzes the reduction of ribonucleotides to deoxyribonucleotides. May function to provide a pool of deoxyribonucleotide precursors for DNA repair during oxygen limitation and/or for immediate growth after restoration of oxygen. http://togogenome.org/gene/1863:CKV89_RS08060 ^@ http://purl.uniprot.org/uniprot/A0A239VMF8 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the GcvH family.|||Binds 1 lipoyl cofactor covalently.|||The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein.|||The glycine cleavage system is composed of four proteins: P, T, L and H. http://togogenome.org/gene/1863:CKV89_RS04735 ^@ http://purl.uniprot.org/uniprot/A0A239VFG1 ^@ Similarity ^@ Belongs to the methylmalonyl-CoA epimerase family. http://togogenome.org/gene/1863:CKV89_RS10700 ^@ http://purl.uniprot.org/uniprot/A0A239VTR5 ^@ Similarity ^@ Belongs to the succinate dehydrogenase/fumarate reductase iron-sulfur protein family. http://togogenome.org/gene/1863:CKV89_RS01790 ^@ http://purl.uniprot.org/uniprot/A0A239V7C5 ^@ Similarity ^@ Belongs to the YciI family. http://togogenome.org/gene/1863:CKV89_RS05435 ^@ http://purl.uniprot.org/uniprot/A0A239VFW4 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the ArgR family.|||Cytoplasm|||Regulates arginine biosynthesis genes. http://togogenome.org/gene/1863:CKV89_RS03695 ^@ http://purl.uniprot.org/uniprot/A0A239VC17 ^@ Function|||Similarity ^@ Belongs to the LDH/MDH superfamily. MDH type 2 family.|||Catalyzes the reversible oxidation of malate to oxaloacetate. http://togogenome.org/gene/1863:CKV89_RS01145 ^@ http://purl.uniprot.org/uniprot/A0A239V5U0 ^@ Cofactor|||Similarity ^@ Belongs to the Fur family.|||Binds 1 Mn(2+) or Fe(2+) ion per subunit.|||Binds 1 zinc ion per subunit. http://togogenome.org/gene/1863:CKV89_RS05455 ^@ http://purl.uniprot.org/uniprot/A0A239VFD0 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the CbiN family.|||Cell membrane|||Forms an energy-coupling factor (ECF) transporter complex composed of an ATP-binding protein (A component, CbiO), a transmembrane protein (T component, CbiQ) and 2 possible substrate-capture proteins (S components, CbiM and CbiN) of unknown stoichimetry.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import. http://togogenome.org/gene/1863:CKV89_RS09620 ^@ http://purl.uniprot.org/uniprot/A0A239VPB0 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the peroxiredoxin family. AhpC/Prx1 subfamily.|||Cytoplasm|||Homodimer.|||Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides. http://togogenome.org/gene/1863:CKV89_RS00220 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YTE3 ^@ Caution|||Similarity|||Subcellular Location Annotation ^@ Belongs to the GtrA family.|||Membrane|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS05030 ^@ http://purl.uniprot.org/uniprot/A0A239VFJ3 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the NAD-dependent glycerol-3-phosphate dehydrogenase family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS05910 ^@ http://purl.uniprot.org/uniprot/A0A239VGF9 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps: L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp/Asn).|||Belongs to the class-II aminoacyl-tRNA synthetase family. Type 1 subfamily.|||Cytoplasm|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS06795 ^@ http://purl.uniprot.org/uniprot/A0A239VJ96 ^@ Similarity ^@ Belongs to the disproportionating enzyme family. http://togogenome.org/gene/1863:CKV89_RS03490 ^@ http://purl.uniprot.org/uniprot/A0A239VB99 ^@ Similarity ^@ Belongs to the ABC transporter superfamily. http://togogenome.org/gene/1863:CKV89_RS06060 ^@ http://purl.uniprot.org/uniprot/A0A239VH36 ^@ Cofactor|||Miscellaneous|||Similarity ^@ Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family.|||Binds 1 FAD per subunit.|||The active site is a redox-active disulfide bond. http://togogenome.org/gene/1863:CKV89_RS06375 ^@ http://purl.uniprot.org/uniprot/A0A239VJ98 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the HPF/YfiA ribosome-associated protein family. Long HPF subfamily.|||Cytoplasm|||Interacts with 100S ribosomes.|||Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase; 100S ribosomes are translationally inactive and sometimes present during exponential growth. http://togogenome.org/gene/1863:CKV89_RS03815 ^@ http://purl.uniprot.org/uniprot/A0A239VDX6 ^@ Function|||Similarity ^@ Belongs to the AIR carboxylase family. Class I subfamily.|||Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR). http://togogenome.org/gene/1863:CKV89_RS03020 ^@ http://purl.uniprot.org/uniprot/A0A239VCA5 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09565 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UDI4 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS01045 ^@ http://purl.uniprot.org/uniprot/A0A239V5K1 ^@ Similarity ^@ Belongs to the citrate synthase family. http://togogenome.org/gene/1863:CKV89_RS10380 ^@ http://purl.uniprot.org/uniprot/A0A239VT95 ^@ Caution|||Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the UPP synthase family.|||Binds 2 magnesium ions per subunit.|||Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids.|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS11355 ^@ http://purl.uniprot.org/uniprot/A0A239VWM3 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Bacterial flagellum|||Belongs to the bacterial flagellin family.|||Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella.|||Secreted http://togogenome.org/gene/1863:CKV89_RS00795 ^@ http://purl.uniprot.org/uniprot/A0A239V4S2 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the AzlC family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS12565 ^@ http://purl.uniprot.org/uniprot/A0A239VQU3 ^@ Similarity ^@ Belongs to the helicase family. UvrD subfamily. http://togogenome.org/gene/1863:CKV89_RS10400 ^@ http://purl.uniprot.org/uniprot/A0A239VT12 ^@ Function|||Similarity ^@ Belongs to the GreA/GreB family.|||Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides. http://togogenome.org/gene/1863:CKV89_RS09425 ^@ http://purl.uniprot.org/uniprot/A0A239VPI6 ^@ Similarity ^@ Belongs to the inositol monophosphatase superfamily. http://togogenome.org/gene/1863:CKV89_RS03860 ^@ http://purl.uniprot.org/uniprot/A0A239VE06 ^@ Similarity ^@ Belongs to the aldehyde dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS00015 ^@ http://purl.uniprot.org/uniprot/A0A239V2S4 ^@ Function ^@ Catalyzes the phosphorylation of hydroxymethylpyrimidine phosphate (HMP-P) to HMP-PP, and of HMP to HMP-P. http://togogenome.org/gene/1863:CKV89_RS06115 ^@ http://purl.uniprot.org/uniprot/A0A239VH78 ^@ Cofactor|||Similarity ^@ Belongs to the PyrK family.|||Binds 1 FAD per subunit.|||Binds 1 [2Fe-2S] cluster per subunit. http://togogenome.org/gene/1863:CKV89_RS04965 ^@ http://purl.uniprot.org/uniprot/A0A239VF35 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the DeoC/FbaB aldolase family. DeoC type 1 subfamily.|||Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy-D-ribose 5-phosphate.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS02550 ^@ http://purl.uniprot.org/uniprot/A0A239VAY2 ^@ Caution|||Function|||Similarity|||Subunit ^@ Belongs to the type-I 3-dehydroquinase family.|||Homodimer.|||Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3-dehydroshikimate.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS04710 ^@ http://purl.uniprot.org/uniprot/A0A239VDL3 ^@ Similarity ^@ Belongs to the Cob(I)alamin adenosyltransferase family. http://togogenome.org/gene/1863:CKV89_RS02935 ^@ http://purl.uniprot.org/uniprot/A0A239VBB6 ^@ Function|||Similarity ^@ Belongs to the aspartokinase family.|||Catalyzes the phosphorylation of the beta-carboxyl group of aspartic acid with ATP to yield 4-phospho-L-aspartate, which is involved in the branched biosynthetic pathway leading to the biosynthesis of amino acids lysine, threonine, isoleucine and methionine. http://togogenome.org/gene/1863:CKV89_RS05065 ^@ http://purl.uniprot.org/uniprot/A0A239VEE2 ^@ Similarity ^@ Belongs to the bacterial ribosomal protein bL28 family. http://togogenome.org/gene/1863:CKV89_RS07360 ^@ http://purl.uniprot.org/uniprot/A0A239VLD6 ^@ Function|||Similarity ^@ Belongs to the HrcA family.|||Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. http://togogenome.org/gene/1863:CKV89_RS03390 ^@ http://purl.uniprot.org/uniprot/A0A239VD28 ^@ Caution|||Function|||Similarity ^@ Belongs to the enoyl-CoA hydratase/isomerase family. MenB subfamily.|||Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4-dihydroxy-2-naphthoyl-CoA (DHNA-CoA).|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS06715 ^@ http://purl.uniprot.org/uniprot/A0A239VJF8 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the OXA1/ALB3/YidC family. Type 1 subfamily.|||Interacts with the Sec translocase complex via SecD. Specifically interacts with transmembrane segments of nascent integral membrane proteins during membrane integration.|||Membrane|||Required for the insertion and/or proper folding and/or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins. Aids folding of multispanning membrane proteins. http://togogenome.org/gene/1863:CKV89_RS08250 ^@ http://purl.uniprot.org/uniprot/A0A239VMG3 ^@ Similarity ^@ Belongs to the Pup ligase/Pup deamidase family. Pup deamidase subfamily. http://togogenome.org/gene/1863:CKV89_RS07465 ^@ http://purl.uniprot.org/uniprot/A0A239VJU7 ^@ Cofactor|||Domain|||Function|||Similarity|||Subunit ^@ Belongs to the DnaG primase family.|||Binds 1 zinc ion per monomer.|||Contains an N-terminal zinc-binding domain, a central core domain that contains the primase activity, and a C-terminal DnaB-binding domain.|||Monomer. Interacts with DnaB.|||RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication. http://togogenome.org/gene/1863:CKV89_RS07510 ^@ http://purl.uniprot.org/uniprot/A0A239VJT9 ^@ Function|||Similarity ^@ Belongs to the thiolase-like superfamily. Beta-ketoacyl-ACP synthases family.|||Involved in the type II fatty acid elongation cycle. Catalyzes the elongation of a wide range of acyl-ACP by the addition of two carbons from malonyl-ACP to an acyl acceptor. Can efficiently catalyze the conversion of palmitoleoyl-ACP (cis-hexadec-9-enoyl-ACP) to cis-vaccenoyl-ACP (cis-octadec-11-enoyl-ACP), an essential step in the thermal regulation of fatty acid composition. http://togogenome.org/gene/1863:CKV89_RS08935 ^@ http://purl.uniprot.org/uniprot/A0A239VP35 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS10360 ^@ http://purl.uniprot.org/uniprot/A0A239VRI9 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the P-Pant transferase superfamily. AcpS family.|||Cytoplasm|||Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein. http://togogenome.org/gene/1863:CKV89_RS00575 ^@ http://purl.uniprot.org/uniprot/A0A239V457 ^@ Similarity ^@ Belongs to the peptidase M18 family. http://togogenome.org/gene/1863:CKV89_RS08615 ^@ http://purl.uniprot.org/uniprot/A0A239VLX4 ^@ Similarity|||Subunit ^@ Belongs to the transketolase family.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS04910 ^@ http://purl.uniprot.org/uniprot/A0A239VDW6 ^@ Caution|||Cofactor|||Function|||Similarity ^@ Belongs to the ketol-acid reductoisomerase family.|||Binds 2 magnesium ions per subunit.|||Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol-acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3-dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3-hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS09645 ^@ http://purl.uniprot.org/uniprot/A0A239VQQ1 ^@ Cofactor|||Function ^@ Binds 1 [3Fe-4S] cluster.|||Ferredoxins are iron-sulfur proteins that transfer electrons in a wide variety of metabolic reactions. http://togogenome.org/gene/1863:CKV89_RS05780 ^@ http://purl.uniprot.org/uniprot/A0A239VHV6 ^@ Function|||Similarity ^@ Belongs to the bacterial ribosomal protein bL20 family.|||Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit. http://togogenome.org/gene/1863:CKV89_RS03575 ^@ http://purl.uniprot.org/uniprot/A0A239VBN3 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the DcuA/DcuB transporter (TC 2.A.13.1) family.|||Cell inner membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS11465 ^@ http://purl.uniprot.org/uniprot/A0A239VV12 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the adenylosuccinate synthetase family.|||Binds 1 Mg(2+) ion per subunit.|||Cytoplasm|||Homodimer.|||Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP. http://togogenome.org/gene/1863:CKV89_RS03525 ^@ http://purl.uniprot.org/uniprot/A0A239VC52 ^@ Similarity ^@ Belongs to the cytochrome P450 family. http://togogenome.org/gene/1863:CKV89_RS00290 ^@ http://purl.uniprot.org/uniprot/A0A239V4V7 ^@ Similarity ^@ Belongs to the lysine N(6)-hydroxylase/L-ornithine N(5)-oxygenase family. http://togogenome.org/gene/1863:CKV89_RS11145 ^@ http://purl.uniprot.org/uniprot/A0A239VVE5 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the FliL family.|||Cell membrane|||Controls the rotational direction of flagella during chemotaxis.|||Membrane http://togogenome.org/gene/1863:CKV89_RS06530 ^@ http://purl.uniprot.org/uniprot/A0A239VJN8 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the PAL/histidase family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS06920 ^@ http://purl.uniprot.org/uniprot/A0A239VIK8 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS05595 ^@ http://purl.uniprot.org/uniprot/A0A239VHG6 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the Iojap/RsfS family.|||Cytoplasm|||Functions as a ribosomal silencing factor. Interacts with ribosomal protein uL14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation.|||Interacts with ribosomal protein uL14 (rplN). http://togogenome.org/gene/1863:CKV89_RS04390 ^@ http://purl.uniprot.org/uniprot/A0A239VEI4 ^@ Similarity ^@ Belongs to the SIMIBI class G3E GTPase family. ArgK/MeaB subfamily. http://togogenome.org/gene/1863:CKV89_RS06575 ^@ http://purl.uniprot.org/uniprot/A0A239VJQ1 ^@ Function|||Similarity ^@ Belongs to the aspartate/glutamate racemases family.|||Provides the (R)-glutamate required for cell wall biosynthesis. http://togogenome.org/gene/1863:CKV89_RS02320 ^@ http://purl.uniprot.org/uniprot/A0A239V991 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the phosphoenolpyruvate carboxykinase [GTP] family.|||Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP), the rate-limiting step in the metabolic pathway that produces glucose from lactate and other precursors derived from the citric acid cycle.|||Cytoplasm|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Monomer. http://togogenome.org/gene/1863:CKV89_RS04105 ^@ http://purl.uniprot.org/uniprot/A0A239VCH0 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the KdpC family.|||Cell membrane|||Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit acts as a catalytic chaperone that increases the ATP-binding affinity of the ATP-hydrolyzing subunit KdpB by the formation of a transient KdpB/KdpC/ATP ternary complex.|||The system is composed of three essential subunits: KdpA, KdpB and KdpC. http://togogenome.org/gene/1863:CKV89_RS00405 ^@ http://purl.uniprot.org/uniprot/A0A239V5U9 ^@ Similarity ^@ Belongs to the carbohydrate kinase PfkB family. http://togogenome.org/gene/1863:CKV89_RS00335 ^@ http://purl.uniprot.org/uniprot/A0A239V604 ^@ Similarity ^@ Belongs to the iron-sulfur dependent L-serine dehydratase family. http://togogenome.org/gene/1863:CKV89_RS09630 ^@ http://purl.uniprot.org/uniprot/A0A239VR46 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the type 2 tetrahydrodipicolinate N-succinyltransferase family.|||Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2-amino-6-oxopimelate using succinyl-CoA.|||Cytoplasm|||Homotrimer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS07755 ^@ http://purl.uniprot.org/uniprot/A0A239VK83 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the peptidase M24A family. Methionine aminopeptidase type 1 subfamily.|||Binds 2 divalent metal cations per subunit. Has a high-affinity and a low affinity metal-binding site. The true nature of the physiological cofactor is under debate. The enzyme is active with cobalt, zinc, manganese or divalent iron ions. Most likely, methionine aminopeptidases function as mononuclear Fe(2+)-metalloproteases under physiological conditions, and the catalytically relevant metal-binding site has been assigned to the histidine-containing high-affinity site.|||Monomer.|||Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed. http://togogenome.org/gene/1863:CKV89_RS02655 ^@ http://purl.uniprot.org/uniprot/A0A239V9M9 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the peptidase M24A family. Methionine aminopeptidase type 1 subfamily.|||Binds 2 divalent metal cations per subunit. Has a high-affinity and a low affinity metal-binding site. The true nature of the physiological cofactor is under debate. The enzyme is active with cobalt, zinc, manganese or divalent iron ions. Most likely, methionine aminopeptidases function as mononuclear Fe(2+)-metalloproteases under physiological conditions, and the catalytically relevant metal-binding site has been assigned to the histidine-containing high-affinity site.|||Monomer.|||Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed. http://togogenome.org/gene/1863:CKV89_RS10280 ^@ http://purl.uniprot.org/uniprot/A0A239VSJ6 ^@ Cofactor|||Similarity ^@ Belongs to the complex I 24 kDa subunit family.|||Binds 1 [2Fe-2S] cluster. http://togogenome.org/gene/1863:CKV89_RS04085 ^@ http://purl.uniprot.org/uniprot/A0A239VCG3 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the amino acid-polyamine-organocation (APC) superfamily. Amino acid transporter (AAT) (TC 2.A.3.1) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS01110 ^@ http://purl.uniprot.org/uniprot/A0A239V5S3 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the nlpA lipoprotein family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS07000 ^@ http://purl.uniprot.org/uniprot/A0A239VK78 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09840 ^@ http://purl.uniprot.org/uniprot/A0A239VQ00 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS4 family.|||One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit.|||Part of the 30S ribosomal subunit. Contacts protein S5. The interaction surface between S4 and S5 is involved in control of translational fidelity.|||With S5 and S12 plays an important role in translational accuracy. http://togogenome.org/gene/1863:CKV89_RS02435 ^@ http://purl.uniprot.org/uniprot/A0A239V8W1 ^@ Similarity ^@ Belongs to the peptidase S1 family. http://togogenome.org/gene/1863:CKV89_RS00325 ^@ http://purl.uniprot.org/uniprot/A0A239V5L3 ^@ Similarity ^@ Belongs to the cytochrome P450 family. http://togogenome.org/gene/1863:CKV89_RS05820 ^@ http://purl.uniprot.org/uniprot/A0A239VGH8 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-I aminoacyl-tRNA synthetase family. TyrS type 1 subfamily.|||Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction: tyrosine is first activated by ATP to form Tyr-AMP and then transferred to the acceptor end of tRNA(Tyr).|||Cytoplasm|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS03365 ^@ http://purl.uniprot.org/uniprot/A0A239VAZ4 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the MenA family. Type 1 subfamily.|||Cell membrane|||Conversion of 1,4-dihydroxy-2-naphthoate (DHNA) to demethylmenaquinone (DMK).|||Membrane http://togogenome.org/gene/1863:CKV89_RS05685 ^@ http://purl.uniprot.org/uniprot/A0A239VG79 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the SepF family.|||Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA.|||Cytoplasm|||Homodimer. Interacts with FtsZ. http://togogenome.org/gene/1863:CKV89_RS02615 ^@ http://purl.uniprot.org/uniprot/A0A239VAP7 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the TerC family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS03000 ^@ http://purl.uniprot.org/uniprot/A0A239VAS7 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily.|||Membrane http://togogenome.org/gene/1863:CKV89_RS09865 ^@ http://purl.uniprot.org/uniprot/A0A239VR76 ^@ Caution|||Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the adenylate kinase family.|||Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism.|||Consists of three domains, a large central CORE domain and two small peripheral domains, NMPbind and LID, which undergo movements during catalysis. The LID domain closes over the site of phosphoryl transfer upon ATP binding. Assembling and dissambling the active center during each catalytic cycle provides an effective means to prevent ATP hydrolysis.|||Cytoplasm|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Monomer. http://togogenome.org/gene/1863:CKV89_RS08035 ^@ http://purl.uniprot.org/uniprot/A0A239VLZ1 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Associates with the 50S ribosomal subunit.|||Belongs to the TRAFAC class TrmE-Era-EngA-EngB-Septin-like GTPase superfamily. EngA (Der) GTPase family.|||Belongs to the cytidylate kinase family. Type 1 subfamily.|||Cytoplasm|||GTPase that plays an essential role in the late steps of ribosome biogenesis. http://togogenome.org/gene/1863:CKV89_RS02290 ^@ http://purl.uniprot.org/uniprot/A0A239VAC4 ^@ Similarity ^@ Belongs to the 6-phosphogluconate dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS06170 ^@ http://purl.uniprot.org/uniprot/A0A239VHB0 ^@ Similarity ^@ Belongs to the class I-like SAM-binding methyltransferase superfamily. RsmB/NOP family. http://togogenome.org/gene/1863:CKV89_RS04795 ^@ http://purl.uniprot.org/uniprot/A0A239VEZ4 ^@ Function|||Subunit ^@ Heterodimer of an alpha and a beta subunit.|||The electron transfer flavoprotein serves as a specific electron acceptor for other dehydrogenases. It transfers the electrons to the main respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase). http://togogenome.org/gene/1863:CKV89_RS11505 ^@ http://purl.uniprot.org/uniprot/A0A239VX49 ^@ Cofactor|||Similarity ^@ Belongs to the DNA repair enzymes AP/ExoA family.|||Probably binds two magnesium or manganese ions per subunit. http://togogenome.org/gene/1863:CKV89_RS08385 ^@ http://purl.uniprot.org/uniprot/A0A239VNC2 ^@ Similarity|||Subunit ^@ Belongs to the NAD(P)-dependent epimerase/dehydratase family.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS03670 ^@ http://purl.uniprot.org/uniprot/A0A239VBS2 ^@ Domain|||Similarity ^@ Belongs to the PurH family.|||The IMP cyclohydrolase activity resides in the N-terminal region. http://togogenome.org/gene/1863:CKV89_RS11460 ^@ http://purl.uniprot.org/uniprot/A0A239VUW3 ^@ Caution|||Similarity|||Subcellular Location Annotation ^@ Belongs to the class-I aminoacyl-tRNA synthetase family.|||Cytoplasm|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS08750 ^@ http://purl.uniprot.org/uniprot/A0A239VNP9 ^@ Similarity|||Subunit ^@ Belongs to the pyruvate kinase family.|||Homotetramer. http://togogenome.org/gene/1863:CKV89_RS08875 ^@ http://purl.uniprot.org/uniprot/A0A239VPG6 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the radical SAM superfamily. Lipoyl synthase family.|||Binds 2 [4Fe-4S] clusters per subunit. One cluster is coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine.|||Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS00465 ^@ http://purl.uniprot.org/uniprot/A0A239V5E6 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS05660 ^@ http://purl.uniprot.org/uniprot/A0A239VH42 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the MurCDEF family.|||Cell wall formation.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS09895 ^@ http://purl.uniprot.org/uniprot/A0A239VQ26 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL6 family.|||Part of the 50S ribosomal subunit.|||This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7/L12 stalk, and near the tRNA binding site of the peptidyltransferase center. http://togogenome.org/gene/1863:CKV89_RS00725 ^@ http://purl.uniprot.org/uniprot/A0A239V6R8 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the cytochrome ubiquinol oxidase subunit 1 family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS05270 ^@ http://purl.uniprot.org/uniprot/A0A239VGB0 ^@ Similarity ^@ Belongs to the UPF0102 family. http://togogenome.org/gene/1863:CKV89_RS11210 ^@ http://purl.uniprot.org/uniprot/A0A239VU29 ^@ Similarity|||Subcellular Location Annotation ^@ Bacterial flagellum basal body|||Belongs to the FliG family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS08290 ^@ http://purl.uniprot.org/uniprot/A0A239VL68 ^@ Function ^@ TetR is the repressor of the tetracycline resistance element; its N-terminal region forms a helix-turn-helix structure and binds DNA. Binding of tetracycline to TetR reduces the repressor affinity for the tetracycline resistance gene (tetA) promoter operator sites. http://togogenome.org/gene/1863:CKV89_RS06620 ^@ http://purl.uniprot.org/uniprot/A0A239VJT0 ^@ Similarity ^@ Belongs to the GroES chaperonin family. http://togogenome.org/gene/1863:CKV89_RS09225 ^@ http://purl.uniprot.org/uniprot/A0A239VQ65 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS10015 ^@ http://purl.uniprot.org/uniprot/A0A239VQH9 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL10 family.|||Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors.|||Part of the ribosomal stalk of the 50S ribosomal subunit. The N-terminus interacts with L11 and the large rRNA to form the base of the stalk. The C-terminus forms an elongated spine to which L12 dimers bind in a sequential fashion forming a multimeric L10(L12)X complex. http://togogenome.org/gene/1863:CKV89_RS08725 ^@ http://purl.uniprot.org/uniprot/A0A239VMC7 ^@ Function|||Similarity ^@ Belongs to the DNA polymerase type-A family.|||In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity. http://togogenome.org/gene/1863:CKV89_RS00140 ^@ http://purl.uniprot.org/uniprot/A0A239V5B3 ^@ Function|||Induction|||Similarity ^@ Acts as a chaperone.|||Belongs to the heat shock protein 70 family.|||By stress conditions e.g. heat shock. http://togogenome.org/gene/1863:CKV89_RS04605 ^@ http://purl.uniprot.org/uniprot/A0A239VDJ9 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the ATPase A chain family.|||Cell membrane|||Key component of the proton channel; it plays a direct role in the translocation of protons across the membrane.|||Membrane http://togogenome.org/gene/1863:CKV89_RS01885 ^@ http://purl.uniprot.org/uniprot/A0A239V7H9 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the UreF family.|||Cytoplasm|||Required for maturation of urease via the functional incorporation of the urease nickel metallocenter.|||UreD, UreF and UreG form a complex that acts as a GTP-hydrolysis-dependent molecular chaperone, activating the urease apoprotein by helping to assemble the nickel containing metallocenter of UreC. The UreE protein probably delivers the nickel. http://togogenome.org/gene/1863:CKV89_RS10345 ^@ http://purl.uniprot.org/uniprot/A0A239VRK5 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the TsaE family.|||Cytoplasm|||Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaD and TsaB. TsaE seems to play an indirect role in the t(6)A biosynthesis pathway, possibly in regulating the core enzymatic function of TsaD. http://togogenome.org/gene/1863:CKV89_RS06000 ^@ http://purl.uniprot.org/uniprot/A0A239VIN3 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the YqgF HJR family.|||Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS04810 ^@ http://purl.uniprot.org/uniprot/A0A239VF08 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the MnmA/TRMU family.|||Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34.|||Cytoplasm|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS02140 ^@ http://purl.uniprot.org/uniprot/A0A239V871 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the OXA1/ALB3/YidC family. Type 1 subfamily.|||Interacts with the Sec translocase complex via SecD. Specifically interacts with transmembrane segments of nascent integral membrane proteins during membrane integration.|||Membrane|||Required for the insertion and/or proper folding and/or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins. Aids folding of multispanning membrane proteins. http://togogenome.org/gene/1863:CKV89_RS09925 ^@ http://purl.uniprot.org/uniprot/A0A239VRF4 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS17 family.|||One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA.|||Part of the 30S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS11300 ^@ http://purl.uniprot.org/uniprot/A0A239VVS5 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the FliS family.|||cytosol http://togogenome.org/gene/1863:CKV89_RS06775 ^@ http://purl.uniprot.org/uniprot/A0A239VIC7 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS08400 ^@ http://purl.uniprot.org/uniprot/A0A239VLD9 ^@ Similarity ^@ Belongs to the UPF0098 family. http://togogenome.org/gene/1863:CKV89_RS01520 ^@ http://purl.uniprot.org/uniprot/A0A239V738 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS03425 ^@ http://purl.uniprot.org/uniprot/A0A239VBZ0 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the GroES chaperonin family.|||Cytoplasm|||Heptamer of 7 subunits arranged in a ring. Interacts with the chaperonin GroEL.|||Together with the chaperonin GroEL, plays an essential role in assisting protein folding. The GroEL-GroES system forms a nano-cage that allows encapsulation of the non-native substrate proteins and provides a physical environment optimized to promote and accelerate protein folding. GroES binds to the apical surface of the GroEL ring, thereby capping the opening of the GroEL channel. http://togogenome.org/gene/1863:CKV89_RS03705 ^@ http://purl.uniprot.org/uniprot/A0A239VCH1 ^@ Cofactor|||Similarity ^@ Belongs to the monomeric-type IDH family.|||Binds 1 Mg(2+) or Mn(2+) ion per subunit. http://togogenome.org/gene/1863:CKV89_RS00980 ^@ http://purl.uniprot.org/uniprot/A0A239V685 ^@ Similarity ^@ Belongs to the aldehyde dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS06430 ^@ http://purl.uniprot.org/uniprot/A0A239VHR9 ^@ Cofactor|||Function|||PTM|||Similarity|||Subcellular Location Annotation ^@ Acts as a transcriptional regulator. Probably redox-responsive. The apo- but not holo-form probably binds DNA.|||Belongs to the WhiB family.|||Binds 1 [4Fe-4S] cluster per subunit. Following nitrosylation of the [4Fe-4S] cluster binds 1 [4Fe-8(NO)] cluster per subunit.|||Cytoplasm|||The Fe-S cluster can be nitrosylated by nitric oxide (NO).|||Upon Fe-S cluster removal intramolecular disulfide bonds are formed. http://togogenome.org/gene/1863:CKV89_RS03415 ^@ http://purl.uniprot.org/uniprot/A0A239VBJ5 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS04435 ^@ http://purl.uniprot.org/uniprot/A0A239VD88 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the chaperonin (HSP60) family.|||Cell surface|||Cytoplasm|||Forms a cylinder of 14 subunits composed of two heptameric rings stacked back-to-back. Interacts with the co-chaperonin GroES.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Together with its co-chaperonin GroES, plays an essential role in assisting protein folding. The GroEL-GroES system forms a nano-cage that allows encapsulation of the non-native substrate proteins and provides a physical environment optimized to promote and accelerate protein folding.|||capsule|||cell wall http://togogenome.org/gene/1863:CKV89_RS02295 ^@ http://purl.uniprot.org/uniprot/A0A239V8G9 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the autoinducer-2 exporter (AI-2E) (TC 2.A.86) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS06935 ^@ http://purl.uniprot.org/uniprot/A0A239VJW8 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS15 family.|||Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome.|||One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it helps nucleate assembly of the platform of the 30S subunit by binding and bridging several RNA helices of the 16S rRNA.|||Part of the 30S ribosomal subunit. Forms a bridge to the 50S subunit in the 70S ribosome, contacting the 23S rRNA. http://togogenome.org/gene/1863:CKV89_RS07905 ^@ http://purl.uniprot.org/uniprot/A0A239VMA3 ^@ Caution|||Cofactor|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-II aminoacyl-tRNA synthetase family.|||Binds 1 zinc ion per subunit.|||Cytoplasm|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS04915 ^@ http://purl.uniprot.org/uniprot/A0A239VFJ4 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the SHMT family.|||Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF-independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism.|||Cytoplasm|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS10155 ^@ http://purl.uniprot.org/uniprot/A0A239VQU4 ^@ Similarity ^@ Belongs to the bacterial ribosomal protein bL32 family. http://togogenome.org/gene/1863:CKV89_RS11120 ^@ http://purl.uniprot.org/uniprot/A0A239VTU5 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the FliQ/MopD/SpaQ family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS04580 ^@ http://purl.uniprot.org/uniprot/A0A239VE79 ^@ Function ^@ Methylates the class 1 translation termination release factors RF1/PrfA and RF2/PrfB on the glutamine residue of the universally conserved GGQ motif. http://togogenome.org/gene/1863:CKV89_RS09990 ^@ http://purl.uniprot.org/uniprot/A0A239VS35 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS7 family.|||One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA.|||Part of the 30S ribosomal subunit. Contacts proteins S9 and S11. http://togogenome.org/gene/1863:CKV89_RS04905 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UBB3 ^@ Caution|||Function|||Similarity|||Subunit ^@ Belongs to the acetolactate synthase small subunit family.|||Catalyzes the conversion of 2 pyruvate molecules into acetolactate in the first common step of the biosynthetic pathway of the branched-amino acids such as leucine, isoleucine, and valine.|||Dimer of large and small chains.|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS09780 ^@ http://purl.uniprot.org/uniprot/A0A239VPV6 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family.|||Cell membrane http://togogenome.org/gene/1863:CKV89_RS05640 ^@ http://purl.uniprot.org/uniprot/A0A239VFX1 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the glycosyltransferase 4 family. MraY subfamily.|||Catalyzes the initial step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan: transfers peptidoglycan precursor phospho-MurNAc-pentapeptide from UDP-MurNAc-pentapeptide onto the lipid carrier undecaprenyl phosphate, yielding undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide, known as lipid I.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS11495 ^@ http://purl.uniprot.org/uniprot/A0A239VVE8 ^@ Similarity ^@ Belongs to the methyl-accepting chemotaxis (MCP) protein family. http://togogenome.org/gene/1863:CKV89_RS00010 ^@ http://purl.uniprot.org/uniprot/A0A239V2R3 ^@ Caution|||Cofactor|||Function|||Similarity ^@ Belongs to the thiamine-phosphate synthase family.|||Binds 1 Mg(2+) ion per subunit.|||Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP).|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS05515 ^@ http://purl.uniprot.org/uniprot/A0A239VG28 ^@ Similarity ^@ Belongs to the ribF family. http://togogenome.org/gene/1863:CKV89_RS03175 ^@ http://purl.uniprot.org/uniprot/A0A239VAN9 ^@ Similarity ^@ Belongs to the DNA glycosylase MPG family. http://togogenome.org/gene/1863:CKV89_RS11170 ^@ http://purl.uniprot.org/uniprot/A0A239VTZ8 ^@ Similarity ^@ Belongs to the flagella basal body rod proteins family. http://togogenome.org/gene/1863:CKV89_RS06745 ^@ http://purl.uniprot.org/uniprot/A0A239VJ67 ^@ Similarity ^@ Belongs to the C/M/P thioester hydrolase family. http://togogenome.org/gene/1863:CKV89_RS03560 ^@ http://purl.uniprot.org/uniprot/A0A239VC75 ^@ Subcellular Location Annotation ^@ Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS02940 ^@ http://purl.uniprot.org/uniprot/A0A239V9W7 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the HAK/KUP transporter (TC 2.A.72) family.|||Cell membrane|||Membrane|||Transport of potassium into the cell. Likely operates as a K(+):H(+) symporter. http://togogenome.org/gene/1863:CKV89_RS04545 ^@ http://purl.uniprot.org/uniprot/A0A239VDB8 ^@ Function|||Similarity|||Subunit ^@ Belongs to the Orn/Lys/Arg decarboxylase class-II family. LysA subfamily.|||Homodimer.|||Specifically catalyzes the decarboxylation of meso-diaminopimelate (meso-DAP) to L-lysine. http://togogenome.org/gene/1863:CKV89_RS01220 ^@ http://purl.uniprot.org/uniprot/A0A239V5Z0 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09995 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UEQ6 ^@ Caution|||Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uS12 family.|||Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit.|||Part of the 30S ribosomal subunit. Contacts proteins S8 and S17. May interact with IF1 in the 30S initiation complex.|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data.|||With S4 and S5 plays an important role in translational accuracy. http://togogenome.org/gene/1863:CKV89_RS09640 ^@ http://purl.uniprot.org/uniprot/A0A239VRB5 ^@ Similarity ^@ Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. http://togogenome.org/gene/1863:CKV89_RS03645 ^@ http://purl.uniprot.org/uniprot/A0A239VBL9 ^@ Function|||Similarity|||Subunit ^@ Belongs to the succinate/malate CoA ligase alpha subunit family.|||Heterotetramer of two alpha and two beta subunits.|||Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit. http://togogenome.org/gene/1863:CKV89_RS07985 ^@ http://purl.uniprot.org/uniprot/A0A239VMG8 ^@ Function|||Similarity ^@ Belongs to the relA/spoT family.|||In eubacteria ppGpp (guanosine 3'-diphosphate 5'-diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance. http://togogenome.org/gene/1863:CKV89_RS00760 ^@ http://purl.uniprot.org/uniprot/A0A239V582 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS05120 ^@ http://purl.uniprot.org/uniprot/A0A239VFX9 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the ribonuclease III family.|||Cytoplasm|||Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre-crRNA and tracrRNA of type II CRISPR loci if present in the organism.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS07585 ^@ http://purl.uniprot.org/uniprot/A0A239VJX5 ^@ Subcellular Location Annotation ^@ Cell inner membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS11275 ^@ http://purl.uniprot.org/uniprot/A0A239VWD5 ^@ Function|||Similarity ^@ Belongs to the NAD(P)-dependent epimerase/dehydratase family. Fucose synthase subfamily.|||Catalyzes the two-step NADP-dependent conversion of GDP-4-dehydro-6-deoxy-D-mannose to GDP-fucose, involving an epimerase and a reductase reaction. http://togogenome.org/gene/1863:CKV89_RS11415 ^@ http://purl.uniprot.org/uniprot/A0A239VUT1 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the AIR synthase family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS07950 ^@ http://purl.uniprot.org/uniprot/A0A239VLS5 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the TACO1 family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS08605 ^@ http://purl.uniprot.org/uniprot/A0A239VNU1 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS04955 ^@ http://purl.uniprot.org/uniprot/A0A239VEC4 ^@ Function|||Similarity ^@ Belongs to the cytidine and deoxycytidylate deaminase family.|||This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis. http://togogenome.org/gene/1863:CKV89_RS02585 ^@ http://purl.uniprot.org/uniprot/A0A239V9A3 ^@ Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-I aminoacyl-tRNA synthetase family.|||Cytoplasm|||Monomer. http://togogenome.org/gene/1863:CKV89_RS03825 ^@ http://purl.uniprot.org/uniprot/A0A239VBX4 ^@ Similarity ^@ Belongs to the glycerate kinase type-1 family. http://togogenome.org/gene/1863:CKV89_RS11440 ^@ http://purl.uniprot.org/uniprot/A0A239VUV8 ^@ Similarity ^@ Belongs to the SAICAR synthetase family. http://togogenome.org/gene/1863:CKV89_RS00740 ^@ http://purl.uniprot.org/uniprot/A0A239V4U4 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS09835 ^@ http://purl.uniprot.org/uniprot/A0A239VRK8 ^@ Domain|||Function|||Similarity|||Subunit ^@ Belongs to the RNA polymerase alpha chain family.|||DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates.|||Homodimer. The RNAP catalytic core consists of 2 alpha, 1 beta, 1 beta' and 1 omega subunit. When a sigma factor is associated with the core the holoenzyme is formed, which can initiate transcription.|||The N-terminal domain is essential for RNAP assembly and basal transcription, whereas the C-terminal domain is involved in interaction with transcriptional regulators and with upstream promoter elements. http://togogenome.org/gene/1863:CKV89_RS10885 ^@ http://purl.uniprot.org/uniprot/A0A239VV42 ^@ Similarity ^@ Belongs to the UDP-N-acetylglucosamine 2-epimerase family. http://togogenome.org/gene/1863:CKV89_RS05465 ^@ http://purl.uniprot.org/uniprot/A0A239VFJ8 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the ABC transporter superfamily.|||Cell membrane|||Part of an ABC transporter complex. Responsible for energy coupling to the transport system. http://togogenome.org/gene/1863:CKV89_RS01545 ^@ http://purl.uniprot.org/uniprot/A0A239V8P8 ^@ Similarity ^@ Belongs to the ThrE exporter (TC 2.A.79) family. http://togogenome.org/gene/1863:CKV89_RS01060 ^@ http://purl.uniprot.org/uniprot/A0A239V5M4 ^@ Similarity ^@ Belongs to the XFP family. http://togogenome.org/gene/1863:CKV89_RS08950 ^@ http://purl.uniprot.org/uniprot/A0A239VPN5 ^@ Similarity ^@ Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family. http://togogenome.org/gene/1863:CKV89_RS00670 ^@ http://purl.uniprot.org/uniprot/A0A239V4L4 ^@ Similarity ^@ Belongs to the TelA family. http://togogenome.org/gene/1863:CKV89_RS10005 ^@ http://purl.uniprot.org/uniprot/A0A239VRQ8 ^@ Function|||Similarity|||Subunit ^@ Belongs to the RNA polymerase beta chain family.|||DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates.|||The RNAP catalytic core consists of 2 alpha, 1 beta, 1 beta' and 1 omega subunit. When a sigma factor is associated with the core the holoenzyme is formed, which can initiate transcription. http://togogenome.org/gene/1863:CKV89_RS03630 ^@ http://purl.uniprot.org/uniprot/A0A239VBR4 ^@ Similarity ^@ Belongs to the helicase family. UvrD subfamily. http://togogenome.org/gene/1863:CKV89_RS06080 ^@ http://purl.uniprot.org/uniprot/A0A239VHY0 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the GPI family.|||Catalyzes the reversible isomerization of glucose-6-phosphate to fructose-6-phosphate.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS11225 ^@ http://purl.uniprot.org/uniprot/A0A239VW64 ^@ Similarity ^@ Belongs to the flagella basal body rod proteins family. http://togogenome.org/gene/1863:CKV89_RS05790 ^@ http://purl.uniprot.org/uniprot/A0A239VG71 ^@ Cofactor|||Similarity ^@ Belongs to the DNA repair enzymes AP/ExoA family.|||Probably binds two magnesium or manganese ions per subunit. http://togogenome.org/gene/1863:CKV89_RS09965 ^@ http://purl.uniprot.org/uniprot/A0A239VS97 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL4 family.|||Forms part of the polypeptide exit tunnel.|||One of the primary rRNA binding proteins, this protein initially binds near the 5'-end of the 23S rRNA. It is important during the early stages of 50S assembly. It makes multiple contacts with different domains of the 23S rRNA in the assembled 50S subunit and ribosome.|||Part of the 50S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS01685 ^@ http://purl.uniprot.org/uniprot/A0A239V718 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS10240 ^@ http://purl.uniprot.org/uniprot/A0A239VSH3 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the complex I subunit 4 family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS07275 ^@ http://purl.uniprot.org/uniprot/A0A239VJI4 ^@ Similarity ^@ Belongs to the IMPACT family. http://togogenome.org/gene/1863:CKV89_RS04800 ^@ http://purl.uniprot.org/uniprot/A0A239VFA8 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the ETF alpha-subunit/FixB family.|||Binds 1 FAD per dimer.|||Heterodimer of an alpha and a beta subunit.|||The electron transfer flavoprotein serves as a specific electron acceptor for other dehydrogenases. It transfers the electrons to the main respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase). http://togogenome.org/gene/1863:CKV89_RS04960 ^@ http://purl.uniprot.org/uniprot/A0A239VE01 ^@ Similarity|||Subunit ^@ Belongs to the thymidine/pyrimidine-nucleoside phosphorylase family.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS01190 ^@ http://purl.uniprot.org/uniprot/A0A239V5S5 ^@ Similarity ^@ Belongs to the glucose-6-phosphate 1-epimerase family. http://togogenome.org/gene/1863:CKV89_RS07960 ^@ http://purl.uniprot.org/uniprot/A0A239VKN9 ^@ Caution|||Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the RuvA family.|||Cytoplasm|||Has three domains with a flexible linker between the domains II and III and assumes an 'L' shape. Domain III is highly mobile and contacts RuvB.|||Homotetramer. Forms an RuvA(8)-RuvB(12)-Holliday junction (HJ) complex. HJ DNA is sandwiched between 2 RuvA tetramers; dsDNA enters through RuvA and exits via RuvB. An RuvB hexamer assembles on each DNA strand where it exits the tetramer. Each RuvB hexamer is contacted by two RuvA subunits (via domain III) on 2 adjacent RuvB subunits; this complex drives branch migration. In the full resolvosome a probable DNA-RuvA(4)-RuvB(12)-RuvC(2) complex forms which resolves the HJ.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||The RuvA-RuvB-RuvC complex processes Holliday junction (HJ) DNA during genetic recombination and DNA repair, while the RuvA-RuvB complex plays an important role in the rescue of blocked DNA replication forks via replication fork reversal (RFR). RuvA specifically binds to HJ cruciform DNA, conferring on it an open structure. The RuvB hexamer acts as an ATP-dependent pump, pulling dsDNA into and through the RuvAB complex. HJ branch migration allows RuvC to scan DNA until it finds its consensus sequence, where it cleaves and resolves the cruciform DNA. http://togogenome.org/gene/1863:CKV89_RS00225 ^@ http://purl.uniprot.org/uniprot/A0A239V429 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the alanine or glycine:cation symporter (AGCS) (TC 2.A.25) family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS03040 ^@ http://purl.uniprot.org/uniprot/A0A239VAD5 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the ribonucleoside diphosphate reductase small chain family.|||Binds 2 iron ions per subunit.|||Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides.|||Tetramer of two alpha and two beta subunits. http://togogenome.org/gene/1863:CKV89_RS08120 ^@ http://purl.uniprot.org/uniprot/A0A239VMK4 ^@ Similarity ^@ Belongs to the peptidase S49 family. http://togogenome.org/gene/1863:CKV89_RS00030 ^@ http://purl.uniprot.org/uniprot/A0A239V4G7 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the amino acid-polyamine-organocation (APC) superfamily. Amino acid transporter (AAT) (TC 2.A.3.1) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS05710 ^@ http://purl.uniprot.org/uniprot/A0A239VG95 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the PEP-utilizing enzyme family.|||Cytoplasm http://togogenome.org/gene/1863:CKV89_RS03715 ^@ http://purl.uniprot.org/uniprot/A0A239VBW6 ^@ Cofactor|||Similarity ^@ Belongs to the DNA repair enzymes AP/ExoA family.|||Probably binds two magnesium or manganese ions per subunit. http://togogenome.org/gene/1863:CKV89_RS00900 ^@ http://purl.uniprot.org/uniprot/A0A239V551 ^@ Cofactor ^@ Binds 4 [4Fe-4S] clusters per subunit. http://togogenome.org/gene/1863:CKV89_RS10350 ^@ http://purl.uniprot.org/uniprot/A0A239VT59 ^@ Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the NnrD/CARKD family.|||Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration.|||Binds 1 potassium ion per subunit.|||Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration.|||Homotetramer.|||In the C-terminal section; belongs to the NnrD/CARKD family.|||In the N-terminal section; belongs to the NnrE/AIBP family. http://togogenome.org/gene/1863:CKV89_RS06940 ^@ http://purl.uniprot.org/uniprot/A0A239VKS7 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the polyribonucleotide nucleotidyltransferase family.|||Cytoplasm|||Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction. http://togogenome.org/gene/1863:CKV89_RS01410 ^@ http://purl.uniprot.org/uniprot/A0A239V7V2 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the inorganic phosphate transporter (PiT) (TC 2.A.20) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS03610 ^@ http://purl.uniprot.org/uniprot/A0A239VBJ0 ^@ Function|||Similarity|||Subunit ^@ Belongs to the class-I fumarase family.|||Catalyzes the reversible hydration of fumarate to (S)-malate.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS00550 ^@ http://purl.uniprot.org/uniprot/A0A239V423 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS04195 ^@ http://purl.uniprot.org/uniprot/A0A239VEJ7 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family. CysTW subfamily.|||Cell membrane|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Membrane|||Part of the binding-protein-dependent transport system for phosphate; probably responsible for the translocation of the substrate across the membrane. http://togogenome.org/gene/1863:CKV89_RS10275 ^@ http://purl.uniprot.org/uniprot/A0A239VRC1 ^@ Function|||Similarity ^@ Belongs to the complex I 51 kDa subunit family.|||NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. http://togogenome.org/gene/1863:CKV89_RS10270 ^@ http://purl.uniprot.org/uniprot/A0A239VR94 ^@ Cofactor|||Function|||Similarity ^@ Belongs to the complex I 75 kDa subunit family.|||Binds 1 [2Fe-2S] cluster per subunit.|||NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. http://togogenome.org/gene/1863:CKV89_RS00005 ^@ http://purl.uniprot.org/uniprot/A0A239V2V2 ^@ Caution|||Function|||Similarity ^@ Belongs to the Thz kinase family.|||Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ).|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS03850 ^@ http://purl.uniprot.org/uniprot/A0A239VDL0 ^@ Activity Regulation|||Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Activated by a monovalent cation that binds near, but not in, the active site. The most likely occupant of the site in vivo is potassium. Ion binding induces a conformational change that may alter substrate affinity.|||Belongs to the carbohydrate kinase PfkB family. Ribokinase subfamily.|||Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5-phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway.|||Cytoplasm|||Homodimer.|||Requires a divalent cation, most likely magnesium in vivo, as an electrophilic catalyst to aid phosphoryl group transfer. It is the chelate of the metal and the nucleotide that is the actual substrate. http://togogenome.org/gene/1863:CKV89_RS06200 ^@ http://purl.uniprot.org/uniprot/A0A239VIZ2 ^@ Function|||Similarity ^@ Belongs to the DMRL synthase family.|||Catalyzes the formation of 6,7-dimethyl-8-ribityllumazine by condensation of 5-amino-6-(D-ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin. http://togogenome.org/gene/1863:CKV89_RS05615 ^@ http://purl.uniprot.org/uniprot/A0A239VGJ7 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the methyltransferase superfamily. RsmH family.|||Cytoplasm|||Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA. http://togogenome.org/gene/1863:CKV89_RS10590 ^@ http://purl.uniprot.org/uniprot/A0A239VU51 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site.|||Cytoplasm|||In the C-terminal section; belongs to the helicase family. RecG subfamily.|||In the N-terminal section; belongs to the UvrB family. http://togogenome.org/gene/1863:CKV89_RS09915 ^@ http://purl.uniprot.org/uniprot/A0A239VRX9 ^@ Function|||Similarity|||Subunit ^@ Belongs to the universal ribosomal protein uL24 family.|||One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit.|||One of two assembly initiator proteins, it binds directly to the 5'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit.|||Part of the 50S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS05390 ^@ http://purl.uniprot.org/uniprot/A0A239VGF1 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-II aminoacyl-tRNA synthetase family. ProS type 1 subfamily.|||Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction: proline is first activated by ATP to form Pro-AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys-tRNA(Pro) is not edited by ProRS.|||Consists of three domains: the N-terminal catalytic domain, the editing domain and the C-terminal anticodon-binding domain.|||Cytoplasm|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS12555 ^@ http://purl.uniprot.org/uniprot/A0A239VNQ8 ^@ Similarity ^@ Belongs to the precorrin methyltransferase family. http://togogenome.org/gene/1863:CKV89_RS01445 ^@ http://purl.uniprot.org/uniprot/A0A239V744 ^@ Caution|||Similarity ^@ Belongs to the globin family.|||In the C-terminal section; belongs to the flavoprotein pyridine nucleotide cytochrome reductase family.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS10100 ^@ http://purl.uniprot.org/uniprot/A0A239VS92 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the PNT beta subunit family.|||Cell inner membrane|||Membrane|||The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane. http://togogenome.org/gene/1863:CKV89_RS07740 ^@ http://purl.uniprot.org/uniprot/A0A239VK81 ^@ Function|||Similarity ^@ Belongs to the IMPDH/GMPR family. GuaB1 subfamily.|||Involved in the purine-salvage pathway. Catalyzes the NADPH-dependent conversion of GMP to IMP. http://togogenome.org/gene/1863:CKV89_RS08435 ^@ http://purl.uniprot.org/uniprot/A0A239VLQ0 ^@ Function|||Similarity|||Subunit ^@ Belongs to the bacterial/plant glucose-1-phosphate adenylyltransferase family.|||Homotetramer.|||Involved in the biosynthesis of ADP-glucose, a building block required for the elongation reactions to produce glycogen. Catalyzes the reaction between ATP and alpha-D-glucose 1-phosphate (G1P) to produce pyrophosphate and ADP-Glc. http://togogenome.org/gene/1863:CKV89_RS05395 ^@ http://purl.uniprot.org/uniprot/A0A239VGK6 ^@ Cofactor|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the RNase H family.|||Binds 1 Mg(2+) ion per subunit. May bind a second metal ion at a regulatory site, or after substrate binding.|||Cytoplasm|||Endonuclease that specifically degrades the RNA of RNA-DNA hybrids.|||Monomer. http://togogenome.org/gene/1863:CKV89_RS02915 ^@ http://purl.uniprot.org/uniprot/A0A239VA16 ^@ Function|||Similarity ^@ Belongs to the RecR family.|||May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO. http://togogenome.org/gene/1863:CKV89_RS11115 ^@ http://purl.uniprot.org/uniprot/A0A239VTV3 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation ^@ Bacterial flagellum basal body|||Belongs to the FliR/MopE/SpaR family.|||Cell membrane|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Membrane|||Role in flagellar biosynthesis. http://togogenome.org/gene/1863:CKV89_RS00415 ^@ http://purl.uniprot.org/uniprot/A0A239V5V9 ^@ Function|||Similarity ^@ Belongs to the iron/manganese superoxide dismutase family.|||Destroys radicals which are normally produced within the cells and which are toxic to biological systems. http://togogenome.org/gene/1863:CKV89_RS06445 ^@ http://purl.uniprot.org/uniprot/A0A239VI26 ^@ Similarity ^@ Belongs to the universal stress protein A family. http://togogenome.org/gene/1863:CKV89_RS04780 ^@ http://purl.uniprot.org/uniprot/A0A239VEY3 ^@ Function|||Similarity|||Subunit ^@ Belongs to the glycosyl hydrolase 13 family. GlgE subfamily.|||Homodimer.|||Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1->4)-glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB. http://togogenome.org/gene/1863:CKV89_RS11400 ^@ http://purl.uniprot.org/uniprot/A0A239VWB4 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Acts as an anti-CsrA protein, binds CsrA and prevents it from repressing translation of its target genes, one of which is flagellin. Binds to flagellin and participates in the assembly of the flagellum.|||Belongs to the FliW family.|||Cytoplasm|||Interacts with translational regulator CsrA and flagellin(s). http://togogenome.org/gene/1863:CKV89_RS09215 ^@ http://purl.uniprot.org/uniprot/A0A239VPK9 ^@ PTM|||Subcellular Location Annotation|||Subunit ^@ Binds 2 heme c groups covalently per subunit.|||Cell membrane|||Membrane|||The cytochrome bc1 complex is composed of a cytochrome b (QcrB), the Rieske iron-sulfur protein (QcrA) and a diheme cytochrome c (QcrC) subunit. http://togogenome.org/gene/1863:CKV89_RS01555 ^@ http://purl.uniprot.org/uniprot/A0A239V6T7 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS08050 ^@ http://purl.uniprot.org/uniprot/A0A239VM01 ^@ Function|||Similarity|||Subunit ^@ Belongs to the polyphosphate kinase 2 (PPK2) family. Class I subfamily.|||Homotetramer.|||Uses inorganic polyphosphate (polyP) as a donor to convert GDP to GTP or ADP to ATP. http://togogenome.org/gene/1863:CKV89_RS07560 ^@ http://purl.uniprot.org/uniprot/A0A239VLB5 ^@ Similarity ^@ Belongs to the GTP cyclohydrolase I type 2/NIF3 family. http://togogenome.org/gene/1863:CKV89_RS09200 ^@ http://purl.uniprot.org/uniprot/A0A239VQC7 ^@ Caution|||Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the anthranilate phosphoribosyltransferase family.|||Binds 2 magnesium ions per monomer.|||Catalyzes the transfer of the phosphoribosyl group of 5-phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA).|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS07975 ^@ http://purl.uniprot.org/uniprot/A0A239VLZ2 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the SecD/SecF family. SecF subfamily.|||Cell membrane|||Forms a complex with SecD. Part of the essential Sec protein translocation apparatus which comprises SecA, SecYEG and auxiliary proteins SecDF. Other proteins may also be involved.|||Membrane|||Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA. http://togogenome.org/gene/1863:CKV89_RS01635 ^@ http://purl.uniprot.org/uniprot/A0A239V701 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the sodium:solute symporter (SSF) (TC 2.A.21) family.|||Catalyzes the sodium-dependent uptake of extracellular L-proline.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS06850 ^@ http://purl.uniprot.org/uniprot/A0A239VJR3 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-I aminoacyl-tRNA synthetase family. ValS type 2 subfamily.|||Catalyzes the attachment of valine to tRNA(Val). As ValRS can inadvertently accommodate and process structurally similar amino acids such as threonine, to avoid such errors, it has a 'posttransfer' editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner.|||Cytoplasm|||Monomer.|||ValRS has two distinct active sites: one for aminoacylation and one for editing. The misactivated threonine is translocated from the active site to the editing site. http://togogenome.org/gene/1863:CKV89_RS02055 ^@ http://purl.uniprot.org/uniprot/A0A239V9D0 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS08560 ^@ http://purl.uniprot.org/uniprot/A0A239VNH6 ^@ Similarity ^@ Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. Csd subfamily. http://togogenome.org/gene/1863:CKV89_RS09210 ^@ http://purl.uniprot.org/uniprot/A0A239VP27 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the cytochrome c oxidase subunit 3 family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS05885 ^@ http://purl.uniprot.org/uniprot/A0A239VH13 ^@ Similarity ^@ Belongs to the aldehyde dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS09385 ^@ http://purl.uniprot.org/uniprot/A0A239VQJ9 ^@ Similarity ^@ Belongs to the UDP-glucose/GDP-mannose dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS02780 ^@ http://purl.uniprot.org/uniprot/A0A239V9M6 ^@ Similarity ^@ Belongs to the CobT family. http://togogenome.org/gene/1863:CKV89_RS06590 ^@ http://purl.uniprot.org/uniprot/A0A239VJA1 ^@ Caution|||Cofactor|||Function|||Similarity|||Subunit ^@ Belongs to the HAM1 NTPase family.|||Binds 1 Mg(2+) ion per subunit.|||Homodimer.|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA/RNA and avoiding chromosomal lesions. http://togogenome.org/gene/1863:CKV89_RS05870 ^@ http://purl.uniprot.org/uniprot/A0A239VHY9 ^@ Activity Regulation|||Caution|||Function|||Miscellaneous|||Similarity|||Subunit ^@ Allosterically activated by GTP, when glutamine is the substrate; GTP has no effect on the reaction when ammonia is the substrate. The allosteric effector GTP functions by stabilizing the protein conformation that binds the tetrahedral intermediate(s) formed during glutamine hydrolysis. Inhibited by the product CTP, via allosteric rather than competitive inhibition.|||Belongs to the CTP synthase family.|||CTPSs have evolved a hybrid strategy for distinguishing between UTP and CTP. The overlapping regions of the product feedback inhibitory and substrate sites recognize a common feature in both compounds, the triphosphate moiety. To differentiate isosteric substrate and product pyrimidine rings, an additional pocket far from the expected kinase/ligase catalytic site, specifically recognizes the cytosine and ribose portions of the product inhibitor.|||Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates.|||Homotetramer.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS06305 ^@ http://purl.uniprot.org/uniprot/A0A239VIC9 ^@ Cofactor|||Function|||PTM|||Similarity|||Subcellular Location Annotation ^@ Acts as a transcriptional regulator. Probably redox-responsive. The apo- but not holo-form probably binds DNA.|||Belongs to the WhiB family.|||Binds 1 [4Fe-4S] cluster per subunit. Following nitrosylation of the [4Fe-4S] cluster binds 1 [4Fe-8(NO)] cluster per subunit.|||Cytoplasm|||The Fe-S cluster can be nitrosylated by nitric oxide (NO).|||Upon Fe-S cluster removal intramolecular disulfide bonds are formed. http://togogenome.org/gene/1863:CKV89_RS04620 ^@ http://purl.uniprot.org/uniprot/A0A239VEX7 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the ATPase delta chain family.|||Cell membrane|||F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation.|||This protein is part of the stalk that links CF(0) to CF(1). It either transmits conformational changes from CF(0) to CF(1) or is implicated in proton conduction. http://togogenome.org/gene/1863:CKV89_RS03440 ^@ http://purl.uniprot.org/uniprot/A0A239VBD1 ^@ Cofactor|||Function|||PTM|||Similarity|||Subcellular Location Annotation ^@ Acts as a transcriptional regulator. Probably redox-responsive. The apo- but not holo-form probably binds DNA.|||Belongs to the WhiB family.|||Binds 1 [4Fe-4S] cluster per subunit. Following nitrosylation of the [4Fe-4S] cluster binds 1 [4Fe-8(NO)] cluster per subunit.|||Cytoplasm|||The Fe-S cluster can be nitrosylated by nitric oxide (NO).|||Upon Fe-S cluster removal intramolecular disulfide bonds are formed. http://togogenome.org/gene/1863:CKV89_RS04395 ^@ http://purl.uniprot.org/uniprot/A0A239VDV0 ^@ Subunit ^@ Heterodimer of an alpha and a beta chain. http://togogenome.org/gene/1863:CKV89_RS10200 ^@ http://purl.uniprot.org/uniprot/A0A239VR22 ^@ Similarity ^@ Belongs to the asparaginase 1 family. http://togogenome.org/gene/1863:CKV89_RS03565 ^@ http://purl.uniprot.org/uniprot/A0A239VC72 ^@ Function|||Subunit ^@ Catalyzes the synthesis of GMP from XMP.|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS01525 ^@ http://purl.uniprot.org/uniprot/A0A239V6Q9 ^@ Similarity ^@ Belongs to the DapA family. http://togogenome.org/gene/1863:CKV89_RS03330 ^@ http://purl.uniprot.org/uniprot/A0A239VAW2 ^@ Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. HemL subfamily.|||Cytoplasm|||Homodimer. http://togogenome.org/gene/1863:CKV89_RS07575 ^@ http://purl.uniprot.org/uniprot/A0A239VL98 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the PEP-utilizing enzyme family.|||Cytoplasm|||General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr). http://togogenome.org/gene/1863:CKV89_RS04405 ^@ http://purl.uniprot.org/uniprot/A0A239VEJ0 ^@ Similarity ^@ Belongs to the precorrin methyltransferase family. http://togogenome.org/gene/1863:CKV89_RS12095 ^@ http://purl.uniprot.org/uniprot/A0A239V4B8 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the GrpE family.|||Cytoplasm|||Homodimer.|||Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ; upon interaction with the DnaJ-bound protein, DnaK hydrolyzes its bound ATP, resulting in the formation of a stable complex. GrpE releases ADP from DnaK; ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. http://togogenome.org/gene/1863:CKV89_RS02410 ^@ http://purl.uniprot.org/uniprot/A0A239V9H8 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the peptide transporter carbon starvation (CstA) (TC 2.A.114) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS10010 ^@ http://purl.uniprot.org/uniprot/A0A239VS28 ^@ Function|||Similarity|||Subunit ^@ Belongs to the bacterial ribosomal protein bL12 family.|||Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation.|||Homodimer. Part of the ribosomal stalk of the 50S ribosomal subunit. Forms a multimeric L10(L12)X complex, where L10 forms an elongated spine to which 2 to 4 L12 dimers bind in a sequential fashion. Binds GTP-bound translation factors. http://togogenome.org/gene/1863:CKV89_RS01295 ^@ http://purl.uniprot.org/uniprot/A0A239V6L9 ^@ Function|||Miscellaneous|||Similarity|||Subcellular Location Annotation ^@ Bacitracin is thought to be involved in the inhibition of peptidoglycan synthesis by sequestering undecaprenyl diphosphate, thereby reducing the pool of lipid carrier available.|||Belongs to the UppP family.|||Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS05370 ^@ http://purl.uniprot.org/uniprot/A0A239VEV4 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS04310 ^@ http://purl.uniprot.org/uniprot/A0A239VEP0 ^@ Similarity ^@ Belongs to the zinc-containing alcohol dehydrogenase family. http://togogenome.org/gene/1863:CKV89_RS03955 ^@ http://purl.uniprot.org/uniprot/A0A239VCY4 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily.|||Membrane http://togogenome.org/gene/1863:CKV89_RS02795 ^@ http://purl.uniprot.org/uniprot/A0A239VA04 ^@ Similarity ^@ Belongs to the cysteine synthase/cystathionine beta-synthase family. http://togogenome.org/gene/1863:CKV89_RS09220 ^@ http://purl.uniprot.org/uniprot/A0A239VQ04 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the Rieske iron-sulfur protein family.|||Cell membrane|||Iron-sulfur subunit of the cytochrome bc1 complex, an essential component of the respiratory electron transport chain required for ATP synthesis. The bc1 complex catalyzes the oxidation of menaquinol and the reduction of cytochrome c in the respiratory chain. The bc1 complex operates through a Q-cycle mechanism that couples electron transfer to generation of the proton gradient that drives ATP synthesis. http://togogenome.org/gene/1863:CKV89_RS10520 ^@ http://purl.uniprot.org/uniprot/A0A239VTV6 ^@ Caution|||Function|||Similarity ^@ Belongs to the NAD(P)-dependent epimerase/dehydratase family. GDP-mannose 4,6-dehydratase subfamily.|||Catalyzes the conversion of GDP-D-mannose to GDP-4-dehydro-6-deoxy-D-mannose.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS00515 ^@ http://purl.uniprot.org/uniprot/A0A239V4G2 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the autoinducer-2 exporter (AI-2E) (TC 2.A.86) family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS10165 ^@ http://purl.uniprot.org/uniprot/A0A239VSJ1 ^@ Similarity|||Subunit ^@ Belongs to the bacterial ribosomal protein bL31 family. Type B subfamily.|||Part of the 50S ribosomal subunit. http://togogenome.org/gene/1863:CKV89_RS00810 ^@ http://purl.uniprot.org/uniprot/A0A239V7G2 ^@ Function|||Similarity|||Subcellular Location Annotation ^@ Belongs to the FdhD family.|||Cytoplasm|||Required for formate dehydrogenase (FDH) activity. Acts as a sulfur carrier protein that transfers sulfur from IscS to the molybdenum cofactor prior to its insertion into FDH. http://togogenome.org/gene/1863:CKV89_RS06980 ^@ http://purl.uniprot.org/uniprot/A0A239VK70 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the ABC-3 integral membrane protein family.|||Cell membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS05760 ^@ http://purl.uniprot.org/uniprot/A0A239VHZ0 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the DcuA/DcuB transporter (TC 2.A.13.1) family.|||Cell inner membrane|||Membrane http://togogenome.org/gene/1863:CKV89_RS11410 ^@ http://purl.uniprot.org/uniprot/A0A9Q2UE34 ^@ Caution ^@ The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS06320 ^@ http://purl.uniprot.org/uniprot/A0A239VJ83 ^@ Similarity ^@ Belongs to the phosphohexose mutase family. http://togogenome.org/gene/1863:CKV89_RS06385 ^@ http://purl.uniprot.org/uniprot/A0A239VIJ3 ^@ Similarity ^@ Belongs to the peptidase S8 family. http://togogenome.org/gene/1863:CKV89_RS04095 ^@ http://purl.uniprot.org/uniprot/A0A239VEF0 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the KdpA family.|||Cell membrane|||Lacks conserved residue(s) required for the propagation of feature annotation.|||Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit binds the extracellular potassium ions and delivers the ions to the membrane domain of KdpB through an intramembrane tunnel.|||The system is composed of three essential subunits: KdpA, KdpB and KdpC. http://togogenome.org/gene/1863:CKV89_RS04240 ^@ http://purl.uniprot.org/uniprot/A0A239VCT1 ^@ Caution|||Cofactor|||Domain|||Function|||Similarity ^@ Belongs to the nitrobindin family.|||Binds 1 heme b group per subunit, that coordinates a highly solvent-exposed Fe(III) atom.|||Forms a 10-stranded antiparallel beta-barrel structure able to accommodate a hydrophobic ligand in its interior. In fact, this fold hosts the heme group, which is located in a wide surface cleft.|||Heme-binding protein able to scavenge peroxynitrite and to protect free L-tyrosine against peroxynitrite-mediated nitration, by acting as a peroxynitrite isomerase that converts peroxynitrite to nitrate. Therefore, this protein likely plays a role in peroxynitrite sensing and in the detoxification of reactive nitrogen and oxygen species (RNS and ROS, respectively). Is able to bind nitric oxide (NO) in vitro, but may act as a sensor of peroxynitrite levels in vivo.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS06835 ^@ http://purl.uniprot.org/uniprot/A0A9Q2YU30 ^@ Caution|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the peptidase S14 family.|||Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins.|||Cytoplasm|||Fourteen ClpP subunits assemble into 2 heptameric rings which stack back to back to give a disk-like structure with a central cavity, resembling the structure of eukaryotic proteasomes.|||The sequence shown here is derived from an EMBL/GenBank/DDBJ whole genome shotgun (WGS) entry which is preliminary data. http://togogenome.org/gene/1863:CKV89_RS01165 ^@ http://purl.uniprot.org/uniprot/A0A239V689 ^@ Similarity ^@ To bacterial alkanal monooxygenase alpha and beta chains. http://togogenome.org/gene/1863:CKV89_RS05245 ^@ http://purl.uniprot.org/uniprot/A0A239VFR9 ^@ Similarity ^@ Belongs to the DyP-type peroxidase family. http://togogenome.org/gene/1863:CKV89_RS11475 ^@ http://purl.uniprot.org/uniprot/A0A239VVC5 ^@ Cofactor|||Function|||Similarity ^@ Belongs to the class II fructose-bisphosphate aldolase family.|||Binds 2 Zn(2+) ions per subunit. One is catalytic and the other provides a structural contribution.|||Catalyzes the aldol condensation of dihydroxyacetone phosphate (DHAP or glycerone-phosphate) with glyceraldehyde 3-phosphate (G3P) to form fructose 1,6-bisphosphate (FBP) in gluconeogenesis and the reverse reaction in glycolysis. http://togogenome.org/gene/1863:CKV89_RS10195 ^@ http://purl.uniprot.org/uniprot/A0A239VSA6 ^@ Similarity ^@ Belongs to the UPF0234 family. http://togogenome.org/gene/1863:CKV89_RS09360 ^@ http://purl.uniprot.org/uniprot/A0A239VQQ4 ^@ Similarity ^@ Belongs to the UDP-N-acetylglucosamine 2-epimerase family. http://togogenome.org/gene/1863:CKV89_RS11135 ^@ http://purl.uniprot.org/uniprot/A0A239VV36 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the FliN/MopA/SpaO family.|||Membrane http://togogenome.org/gene/1863:CKV89_RS02725 ^@ http://purl.uniprot.org/uniprot/A0A239VAZ1 ^@ Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the ThiG family.|||Catalyzes the rearrangement of 1-deoxy-D-xylulose 5-phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S.|||Cytoplasm|||Homotetramer. Forms heterodimers with either ThiH or ThiS. http://togogenome.org/gene/1863:CKV89_RS08705 ^@ http://purl.uniprot.org/uniprot/A0A239VNU8 ^@ Domain|||Function|||Similarity|||Subcellular Location Annotation|||Subunit ^@ Belongs to the UvrB family.|||Cytoplasm|||Forms a heterotetramer with UvrA during the search for lesions. Interacts with UvrC in an incision complex.|||The UvrABC repair system catalyzes the recognition and processing of DNA lesions. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. Upon binding of the UvrA(2)B(2) complex to a putative damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage.|||The beta-hairpin motif is involved in DNA binding. http://togogenome.org/gene/1863:CKV89_RS01455 ^@ http://purl.uniprot.org/uniprot/A0A239V6L1 ^@ Function|||Similarity ^@ Belongs to the AlaDH/PNT family.|||Catalyzes the reversible reductive amination of pyruvate to L-alanine. http://togogenome.org/gene/1863:CKV89_RS03030 ^@ http://purl.uniprot.org/uniprot/A0A239VBU3 ^@ Function|||Similarity ^@ Belongs to the NrdI family.|||Probably involved in ribonucleotide reductase function. http://togogenome.org/gene/1863:CKV89_RS06165 ^@ http://purl.uniprot.org/uniprot/A0A239VIW8 ^@ Function|||Similarity ^@ Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus.|||Belongs to the Fmt family. http://togogenome.org/gene/1863:CKV89_RS06650 ^@ http://purl.uniprot.org/uniprot/A0A239VHZ1 ^@ Similarity ^@ Belongs to the carbon-nitrogen hydrolase superfamily. NIT1/NIT2 family. http://togogenome.org/gene/1863:CKV89_RS04770 ^@ http://purl.uniprot.org/uniprot/A0A239VF88 ^@ Function|||Similarity|||Subunit ^@ Belongs to the aminoglycoside phosphotransferase family.|||Belongs to the glycosyl hydrolase 13 family. GlgB subfamily.|||Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position.|||Monomer. http://togogenome.org/gene/1863:CKV89_RS04425 ^@ http://purl.uniprot.org/uniprot/A0A239VEU7 ^@ Similarity ^@ Belongs to the LysR transcriptional regulatory family. http://togogenome.org/gene/1863:CKV89_RS03865 ^@ http://purl.uniprot.org/uniprot/A0A239VC61 ^@ Caution|||Function|||Similarity ^@ Belongs to the bacterial two-domain DSD family.|||Catalyzes the conversion of 3-dehydroshikimate to protocatechuate (3,4-dihydroxybenzoate), a common intermediate of quinate and shikimate degradation pathways.|||Lacks conserved residue(s) required for the propagation of feature annotation. http://togogenome.org/gene/1863:CKV89_RS04945 ^@ http://purl.uniprot.org/uniprot/A0A239VF16 ^@ Similarity ^@ Belongs to the SorC transcriptional regulatory family. http://togogenome.org/gene/1863:CKV89_RS04650 ^@ http://purl.uniprot.org/uniprot/A0A239VEZ6 ^@ Similarity ^@ Belongs to the transferase hexapeptide repeat family. http://togogenome.org/gene/1863:CKV89_RS00645 ^@ http://purl.uniprot.org/uniprot/A0A239V4F2 ^@ Subcellular Location Annotation ^@ Membrane http://togogenome.org/gene/1863:CKV89_RS01995 ^@ http://purl.uniprot.org/uniprot/A0A239V7V0 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the binding-protein-dependent transport system permease family.|||Cell membrane http://togogenome.org/gene/1863:CKV89_RS00200 ^@ http://purl.uniprot.org/uniprot/A0A239V3J9 ^@ Similarity|||Subcellular Location Annotation ^@ Belongs to the branched chain amino acid transporter family.|||Membrane