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nudC | NADH pyrophosphatase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the Nudix hydrolase family. (257 aa) | ||||
nfi | Endonuclease V; DNA repair enzyme involved in the repair of deaminated bases. Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA. (223 aa) | ||||
lysU | Lysine tRNA synthetase, inducible; Function experimentally demonstrated in the studied species; enzyme; Belongs to the class-II aminoacyl-tRNA synthetase family. (505 aa) | ||||
purA | Adenylosuccinate synthetase; 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; Belongs to the adenylosuccinate synthetase family. (432 aa) | ||||
ulaD | 3-keto-L-gulonate 6-phosphate decarboxylase; Catalyzes the decarboxylation of 3-keto-L-gulonate-6-P into L-xylulose-5-P. Is involved in the anaerobic L-ascorbate utilization. Belongs to the HPS/KGPDC family. KGPDC subfamily. (216 aa) | ||||
cysQ | PAPS (adenosine 3'-phosphate 5'-phosphosulfate) 3'(2'),5'-bisphosphate nucleotidase; Function experimentally demonstrated in the studied species; enzyme. (246 aa) | ||||
ppa | Inorganic pyrophosphatase; Function experimentally demonstrated in the studied species; enzyme. (176 aa) | ||||
fbp | Function experimentally demonstrated in the studied species; enzyme. (332 aa) | ||||
deoB | Phosphopentomutase; Phosphotransfer between the C1 and C5 carbon atoms of pentose; Belongs to the phosphopentomutase family. (407 aa) | ||||
dnaT | DNA biosynthesis protein (primosomal protein I); Function experimentally demonstrated in the studied species; factor. (179 aa) | ||||
pdxA | 4-hydroxy-L-threonine phosphate dehydrogenase, NAD-dependent; Catalyzes the NAD(P)-dependent oxidation of 4-(phosphooxy)-L- threonine (HTP) into 2-amino-3-oxo-4-(phosphooxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP). (329 aa) | ||||
leuB | 3-isopropylmalate dehydrogenase; Function experimentally demonstrated in the studied species; enzyme. (363 aa) | ||||
ilvI | Acetolactate synthase III, large subunit; Function experimentally demonstrated in the studied species; enzyme. (574 aa) | ||||
murE | UDP-N-acetylmuramoyl-L-alanyl-D-glutamate:meso- diaminopimelate ligase; Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan. Belongs to the MurCDEF family. MurE subfamily. (495 aa) | ||||
dgt | Deoxyguanosine triphosphate triphosphohydrolase; Function experimentally demonstrated in the studied species; enzyme. (505 aa) | ||||
ispU | Undecaprenyl pyrophosphate synthase; Catalyzes the sequential condensation of isopentenyl diphosphate (IPP) with (2E,6E)-farnesyl diphosphate (E,E-FPP) to yield (2Z,6Z,10Z,14Z,18Z,22Z,26Z,30Z,34E,38E)-undecaprenyl diphosphate (di- trans,octa-cis-UPP). UPP is the precursor of glycosyl carrier lipid in the biosynthesis of bacterial cell wall polysaccharide components such as peptidoglycan and lipopolysaccharide. (253 aa) | ||||
gmhB | D,D-heptose 1,7-bisphosphate phosphatase; Function experimentally demonstrated in the studied species; enzyme. (190 aa) | ||||
rnhA | Ribonuclease HI, degrades RNA of DNA-RNA hybrids; Endonuclease that specifically degrades the RNA of RNA-DNA hybrids. (155 aa) | ||||
dinB | DNA polymerase IV; Function experimentally demonstrated in the studied species; enzyme. (351 aa) | ||||
gpt | Guanine-hypoxanthine phosphoribosyltransferase; Acts on guanine, xanthine and to a lesser extent hypoxanthine; Belongs to the purine/pyrimidine phosphoribosyltransferase family. XGPT subfamily. (152 aa) | ||||
prpB | 2-methylisocitrate lyase; Catalyzes the thermodynamically favored C-C bond cleavage of (2R,3S)-2-methylisocitrate to yield pyruvate and succinate. Belongs to the isocitrate lyase/PEP mutase superfamily. Methylisocitrate lyase family. (296 aa) | ||||
lacZ | beta-D-galactosidase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the glycosyl hydrolase 2 family. (1024 aa) | ||||
aroL | Shikimate kinase II; Function experimentally demonstrated in the studied species; enzyme. (174 aa) | ||||
thiL | Thiamin-monophosphate kinase; Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1; Belongs to the thiamine-monophosphate kinase family. (325 aa) | ||||
dxs | 1-deoxyxylulose-5-phosphate synthase, thiamine-requiring, FAD-requiring; Function experimentally demonstrated in the studied species; enzyme. (620 aa) | ||||
cof | Thiamin pyrimidine pyrophosphate hydrolase; Catalyzes the hydrolysis of 4-amino-2-methyl-5- hydroxymethylpyrimidine pyrophosphate (HMP-PP) to 4-amino-2-methyl-5- hydroxymethylpyrimidine phosphate (HMP-P). Belongs to the HAD-like hydrolase superfamily. Cof family. (272 aa) | ||||
gcl | Glyoxylate carboligase; Function experimentally demonstrated in the studied species; enzyme. (593 aa) | ||||
entD | Phosphopantetheinyltransferase component of enterobactin synthase multienzyme complex; Function experimentally demonstrated in the studied species; enzyme; Belongs to the P-Pant transferase superfamily. (209 aa) | ||||
entC | Isochorismate synthase 1; Function experimentally demonstrated in the studied species; enzyme. (391 aa) | ||||
entB | Isochorismatase; Function experimentally demonstrated in the studied species; enzyme. (285 aa) | ||||
nagD | NMP phosphatase; Function experimentally demonstrated in the studied species; enzyme. (250 aa) | ||||
pgm | Phosphoglucomutase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the phosphohexose mutase family. (546 aa) | ||||
kdpB | Potassium translocating ATPase, subunit B; 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. Belongs to the cation transport ATPase (P-type) (TC 3.A.3) family. Type IA subfamily. (682 aa) | ||||
sucC | succinyl-CoA synthetase, beta subunit; 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. (388 aa) | ||||
galK | Galactokinase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the GHMP kinase family. GalK subfamily. (382 aa) | ||||
ybhA | Putative phosphatase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (272 aa) | ||||
CAQ97625.1 | Conserved hypothetical protein; Homologs of previously reported genes of unknown function. (170 aa) | ||||
rusA | Endonuclease RUS; Function experimentally demonstrated in the studied species; extrachromosomal origin. (120 aa) | ||||
bioD | Dethiobiotin synthetase; Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8- diaminopelargonic acid (DAPA) to form an ureido ring. Belongs to the dethiobiotin synthetase family. (225 aa) | ||||
ybiV | Type II HAD phosphatase; Function experimentally demonstrated in the studied species; enzyme. (271 aa) | ||||
ybjI | Putative phosphatase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (271 aa) | ||||
poxB | Pyruvate dehydrogenase (pyruvate oxidase), thiamin-dependent, FAD-binding; Function experimentally demonstrated in the studied species; enzyme; Belongs to the TPP enzyme family. (572 aa) | ||||
rne | Fused ribonucleaseE: endoribonuclease; Function experimentally demonstrated in the studied species; enzyme. (1061 aa) | ||||
icd | Isocitrate dehydrogenase, specific for NADP+; Function experimentally demonstrated in the studied species; extrachromosomal origin. (416 aa) | ||||
prsA | Phosphoribosylpyrophosphate synthase; Function experimentally demonstrated in the studied species; enzyme. (315 aa) | ||||
trpD | Fused glutamine amidotransferase (component II) of anthranilate synthase; Function experimentally demonstrated in the studied species; enzyme. (531 aa) | ||||
ycjU | Putative glucose-1-phosphate phosphodismutase, beta-phosphoglucomutase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (219 aa) | ||||
ydaO | Putative C32 tRNA thiolase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (311 aa) | ||||
dos | cAMP phosphodiesterase, heme-regulated; Function experimentally demonstrated in the studied species; enzyme. (799 aa) | ||||
rspA | Putative enolase/dehydratase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme; Belongs to the mandelate racemase/muconate lactonizing enzyme family. (404 aa) | ||||
speG | Spermidine N1-acetyltransferase; Function experimentally demonstrated in the studied species; enzyme. (186 aa) | ||||
ynfK | Putative synthase (similar to dethiobiotin synthetase); Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8- diaminopelargonic acid (DAPA) to form an ureido ring. Belongs to the dethiobiotin synthetase family. (231 aa) | ||||
pdxY | Pyridoxal kinase 2/pyridoxine kinase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the pyridoxine kinase family. (287 aa) | ||||
rnt | Ribonuclease T (RNase T); Trims short 3' overhangs of a variety of RNA species, leaving a one or two nucleotide 3' overhang. Responsible for the end-turnover of tRNA: specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis. (215 aa) | ||||
pykF | Pyruvate kinase I; Function experimentally demonstrated in the studied species; enzyme; Belongs to the pyruvate kinase family. (470 aa) | ||||
pheT | Phenylalanine tRNA synthetase, beta subunit; Function experimentally demonstrated in the studied species; enzyme; Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily. (795 aa) | ||||
pheS | Phenylalanine tRNA synthetase, alpha subunit; Function experimentally demonstrated in the studied species; enzyme. (327 aa) | ||||
yniC | Putative phosphoglycolate phosphatase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (222 aa) | ||||
topB | DNA topoisomerase III; Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA- (5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA su [...] (653 aa) | ||||
selD | Selenophosphate synthase; Function experimentally demonstrated in the studied species; enzyme. (347 aa) | ||||
yeaU | Putative tartrate dehydrogenase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (361 aa) | ||||
yeaB | Putative NUDIX hydrolase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme; Belongs to the Nudix hydrolase family. PCD1 subfamily. (192 aa) | ||||
purT | Phosphoribosylglycinamide formyltransferase 2; Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate. Belongs to the PurK/PurT family. (392 aa) | ||||
pykA | Pyruvate kinase II; Function experimentally demonstrated in the studied species; enzyme; Belongs to the pyruvate kinase family. (480 aa) | ||||
ruvC | Component of RuvABC resolvasome, endonuclease; Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group. (173 aa) | ||||
otsB | Trehalose-6-phosphate phosphatase, biosynthetic; Removes the phosphate from trehalose 6-phosphate to produce free trehalose. (266 aa) | ||||
yedP | Putative mannosyl-3-phosphoglycerate phosphatase (mngB-like); Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (271 aa) | ||||
hisG | ATP phosphoribosyltransferase; Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity. (299 aa) | ||||
cpsG | Phosphomannomutase (PMM); Involved in GDP-mannose biosynthesis which serves as the activated sugar nucleotide precursor for mannose residues in cell surface polysaccharides. This enzyme participates in synthesis of the LPS O9 antigen; Belongs to the phosphohexose mutase family. (468 aa) | ||||
cpsG-2 | Phosphomannomutase; Involved in GDP-mannose biosynthesis which serves as the activated sugar nucleotide precursor for mannose residues in cell surface polysaccharides. This enzyme participates in synthesis of the LPS O7 antigen. (456 aa) | ||||
yegS | Conserved hypothetical protein; Probably phosphorylates lipids; the in vivo substrate is unknown; Belongs to the diacylglycerol/lipid kinase family. YegS lipid kinase subfamily. (299 aa) | ||||
thiM | Hydoxyethylthiazole kinase; Catalyzes the phosphorylation of the hydroxyl group of 4- methyl-5-beta-hydroxyethylthiazole (THZ). Belongs to the Thz kinase family. (262 aa) | ||||
yfaO | Putative NUDIX hydrolase; Catalyzes the hydrolysis of nucleoside triphosphates, with a preference for pyrimidine deoxynucleoside triphosphates (dUTP, dTTP and dCTP); Belongs to the Nudix hydrolase family. NudI subfamily. (141 aa) | ||||
menC | o-succinylbenzoyl-CoA synthase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the mandelate racemase/muconate lactonizing enzyme family. (320 aa) | ||||
menD | Bifunctional 2-oxoglutarate decarboxylase and SHCHC synthase; Function experimentally demonstrated in the studied species; enzyme. (556 aa) | ||||
menF | Isochorismate synthase 2; Function experimentally demonstrated in the studied species; enzyme. (431 aa) | ||||
ackA | Acetate kinase A and propionate kinase 2; Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction; Belongs to the acetokinase family. (400 aa) | ||||
purF | Amidophosphoribosyltransferase; Function experimentally demonstrated in the studied species; enzyme. (505 aa) | ||||
oxc | Putative oxalyl-CoA decarboxylase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (564 aa) | ||||
pdxK | Pyridoxal-pyridoxamine kinase/hydroxymethylpyrimidine kinase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the pyridoxine kinase family. (283 aa) | ||||
vapC_2 | Conserved hypothetical protein, putative nucleotide binding protein; Toxic component of a toxin-antitoxin (TA) system. A site- specific tRNA-(fMet) endonuclease, it cleaves both charged and uncharged tRNA-(fMet) between positions 38 and 39 at the anticodon stem-loop boundary. Its toxic effects are neutralized by expression of cognate antitoxin VapB; Belongs to the PINc/VapC protein family. (132 aa) | ||||
upp | Uracil phosphoribosyltransferase; Catalyzes the conversion of uracil and 5-phospho-alpha-D- ribose 1-diphosphate (PRPP) to UMP and diphosphate. (208 aa) | ||||
acpS | Holo-[acyl-carrier-protein] synthase 1; Function experimentally demonstrated in the studied species; enzyme. (126 aa) | ||||
ygcF | Conserved hypothetical protein; Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7-carboxy-7- deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds. (223 aa) | ||||
eno | Enolase; Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis. (432 aa) | ||||
gudD | (D)-glucarate dehydratase 1; Function experimentally demonstrated in the studied species; enzyme; Belongs to the mandelate racemase/muconate lactonizing enzyme family. (446 aa) | ||||
exo | Exonuclease IX (5'-3' exonuclease); Has flap endonuclease activity. During DNA replication, flap endonucleases cleave the 5'-overhanging flap structure that is generated by displacement synthesis when DNA polymerase encounters the 5'-end of a downstream Okazaki fragment. (281 aa) | ||||
recB | Exonuclease V (RecBCD complex), beta subunit; Function experimentally demonstrated in the studied species; enzyme. (1180 aa) | ||||
lysS | Lysine tRNA synthetase, constitutive; Function experimentally demonstrated in the studied species; enzyme; Belongs to the class-II aminoacyl-tRNA synthetase family. (505 aa) | ||||
metK | Methionine adenosyltransferase 1; 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. (384 aa) | ||||
ribB | 3,4-dihydroxy-2-butanone-4-phosphate synthase; Function experimentally demonstrated in the studied species; enzyme. (217 aa) | ||||
glnE | Fused deadenylyltransferase; Function experimentally demonstrated in the studied species; enzyme. (946 aa) | ||||
cca | Fused tRNA nucleotidyl transferase; Function experimentally demonstrated in the studied species; enzyme. (412 aa) | ||||
garL | alpha-dehydro-beta-deoxy-D-glucarate aldolase; Catalyzes the reversible retro-aldol cleavage of both 5-keto- 4-deoxy-D-glucarate and 2-keto-3-deoxy-D-glucarate to pyruvate and tartronic semialdehyde; Belongs to the HpcH/HpaI aldolase family. KDGluc aldolase subfamily. (256 aa) | ||||
pnp | Polynucleotide phosphorylase/polyadenylase; Function experimentally demonstrated in the studied species; enzyme. (734 aa) | ||||
glmM | Phosphoglucosamine mutase; Function experimentally demonstrated in the studied species; enzyme. (445 aa) | ||||
obgE | GTPase involved in cell partioning and DNA repair; An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control. Belongs to the TRAFAC class OBG-HflX-like GTPase superfamily. OBG GTPase family. (390 aa) | ||||
yhfW | Putative mutase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (408 aa) | ||||
aroK | Shikimate kinase I; Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate; Belongs to the shikimate kinase family. (173 aa) | ||||
acpT | Holo-(acyl carrier protein) synthase 2; Function experimentally demonstrated in the studied species; enzyme; Belongs to the P-Pant transferase superfamily. (195 aa) | ||||
xylA | D-xylose isomerase; Function experimentally demonstrated in the studied species; enzyme. (440 aa) | ||||
dut | Deoxyuridinetriphosphatase; This enzyme is involved in nucleotide metabolism: it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA. (151 aa) | ||||
pyrE | Orotate phosphoribosyltransferase; Catalyzes the transfer of a ribosyl phosphate group from 5- phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP). (213 aa) | ||||
ilvB | Acetolactate synthase I, large subunit; Function experimentally demonstrated in the studied species; enzyme. (562 aa) | ||||
dgoD | Galactonate dehydratase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the mandelate racemase/muconate lactonizing enzyme family. (382 aa) | ||||
yidA | Putative hydrolase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (270 aa) | ||||
yieE | Putative phosphopantetheinyl transferase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (253 aa) | ||||
glmU | Fused N-acetyl glucosamine-1-phosphate uridyltransferase; Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP-GlcNAc). The C- terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N- acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5-monophosphate (from uridine 5- triphosphate), a reaction catalyzed by the N-terminal domain. (456 aa) | ||||
ilvG | Acetolactate synthase isozyme II large subunit; Function of strongly homologous gene; enzyme. (548 aa) | ||||
ilvD | Dihydroxyacid dehydratase; Function experimentally demonstrated in the studied species; enzyme; Belongs to the IlvD/Edd family. (616 aa) | ||||
ilvC | Ketol-acid reductoisomerase, NAD(P)-binding; 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. (491 aa) | ||||
rfe | UDP-GlcNAc:undecaprenylphosphate GlcNAc-1-phosphate transferase; Catalyzes the transfer of the GlcNAc-1-phosphate moiety from UDP-GlcNAc onto the carrier lipid undecaprenyl phosphate (C55-P), yielding GlcNAc-pyrophosphoryl-undecaprenyl (GlcNAc-PP-C55). (367 aa) | ||||
yigL | Putative hydrolase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (266 aa) | ||||
tatD | DNase, magnesium-dependent; 3'-5' exonuclease that prefers single-stranded DNA and RNA. May play a role in the H(2)O(2)-induced DNA damage repair. Belongs to the metallo-dependent hydrolases superfamily. TatD-type hydrolase family. TatD subfamily. (260 aa) | ||||
yihE | Putative kinase; Function of strongly homologous gene; putative enzyme. (328 aa) | ||||
ppc | Phosphoenolpyruvate carboxylase; Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle; Belongs to the PEPCase type 1 family. (883 aa) | ||||
rspA-2 | Putative enolase/dehydratase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (424 aa) | ||||
rpoC | RNA polymerase, beta prime subunit; DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates. (1407 aa) | ||||
thiE | Thiamin phosphate synthase (thiamin phosphate pyrophosphorylase); Function experimentally demonstrated in the studied species; enzyme. (211 aa) |