STRINGSTRING
rhmD rhmD thrC thrC caiD caiD leuD leuD leuC leuC acnB acnB speD speD can can panD panD fabZ fabZ ldcC ldcC mltD mltD ROD_03521 ROD_03521 ROD_03531 ROD_03531 prpB prpB prpD prpD hemB hemB ROD_05021 ROD_05021 hemH hemH ROD_05391 ROD_05391 purK purK rna rna citF citF citE citE citC citC rlpA rlpA cobD cobD speF speF phrB phrB ROD_07671 ROD_07671 hutU hutU hutH hutH moaA moaA moaC moaC fsaA fsaA ltaE ltaE ROD_09311 ROD_09311 fabA fabA mgsA mgsA ROD_10731 ROD_10731 pabC pabC mltG mltG purB purB ROD_12381 ROD_12381 ROD_12451 ROD_12451 ROD_12811 ROD_12811 aroD aroD sufS sufS ROD_13791 ROD_13791 gloA gloA nth nth fumA fumA fumC fumC dapA dapA sfcA sfcA ROD_15651 ROD_15651 ROD_16291 ROD_16291 pyrF pyrF acnA acnA trpE trpE trpD trpD trpC trpC trpB trpB trpA trpA chaC chaC mltE mltE sdaA sdaA eda eda edd edd dcyD dcyD cbiK cbiK cbiB cbiB pduC pduC pduD pduD pduE pduE hisB hisB hisH hisH hisF hisF rfbB rfbB gmd gmd ROD_22211 ROD_22211 fbaB fbaB psuG psuG uxuA uxuA cysM cysM eutC eutC eutB eutB eutA eutA maeB maeB dapA-2 dapA-2 mltF mltF murQ murQ ROD_25161 ROD_25161 pheA pheA ROD_25481 ROD_25481 rhmA rhmA menC menC menB menB menH menH folX folX aroC aroC fadJ fadJ ROD_28081 ROD_28081 sdaB sdaB fucA fucA mltA mltA lysA lysA ogl ogl gudX gudX gudD gudD eno eno queE queE ROD_30411 ROD_30411 ispF ispF ROD_30711 ROD_30711 hypE hypE hycA hycA luxS luxS ROD_31591 ROD_31591 ROD_31651 ROD_31651 aspA aspA psd psd nnrD nnrD ulaD ulaD ROD_33061 ROD_33061 ROD_34021 ROD_34021 nrfG nrfG fumB fumB metC metC ribB ribB ROD_36031 ROD_36031 ttdA ttdA ttdB ttdB ROD_36351 ROD_36351 ubiC ubiC aceA aceA hemE hemE thiC thiC thiH thiH argH argH ppc ppc pflC pflC fsaB fsaB ROD_38421 ROD_38421 rhaD rhaD ROD_38801 ROD_38801 fadB fadB ubiD ubiD cyaA cyaA hemD hemD rffG rffG ilvA ilvA ilvD ilvD dgoA dgoA dsdA dsdA coaBC coaBC mutM mutM ROD_42111 ROD_42111 mtlR mtlR ROD_43121 ROD_43121 padC padC ROD_43271 ROD_43271 ROD_43341 ROD_43341 pckA pckA aroB aroB cysG cysG nanA nanA uxuA-2 uxuA-2 elbB elbB gatY gatY garD garD garL garL tdcB tdcB tdcG tdcG ROD_47661 ROD_47661 uxaA uxaA metC-2 metC-2 ROD_48391 ROD_48391 dgoA-2 dgoA-2 deoC deoC speC speC mltC mltC speA speA fbaA fbaA slt slt
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query proteins and first shell of interactors
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second shell of interactors
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proteins of unknown 3D structure
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a 3D structure is known or predicted
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rhmDPutative MR-MLE-family protein; Catalyzes the dehydration of L-rhamnonate to 2-keto-3-deoxy- L-rhamnonate (KDR). (405 aa)
thrCThreonine synthase. (428 aa)
caiDcarnitinyl-CoA dehydratase; Catalyzes the reversible dehydration of L-carnitinyl-CoA to crotonobetainyl-CoA. (261 aa)
leuD3-isopropylmalate dehydratase small subunit; Catalyzes the isomerization between 2-isopropylmalate and 3- isopropylmalate, via the formation of 2-isopropylmaleate. Belongs to the LeuD family. LeuD type 1 subfamily. (201 aa)
leuC3-isopropylmalate dehydratase large subunit; Catalyzes the isomerization between 2-isopropylmalate and 3- isopropylmalate, via the formation of 2-isopropylmaleate. (466 aa)
acnBAconitate hydratase 2 (citrate hydro-lyase 2); Belongs to the aconitase/IPM isomerase family. (865 aa)
speDS-adenosylmethionine decarboxylase proenzyme; Catalyzes the decarboxylation of S-adenosylmethionine to S- adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine; Belongs to the prokaryotic AdoMetDC family. Type 2 subfamily. (264 aa)
canCarbonic anhydrase 2; Reversible hydration of carbon dioxide. Belongs to the beta-class carbonic anhydrase family. (220 aa)
panDAspartate L-decarboxylase; Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine. (126 aa)
fabZ(3r)-hydroxymyristol acyl carrier protein dehydratase (ec 4.2.1.-); Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs. (151 aa)
ldcCLysine decarboxylase, constitutive. (712 aa)
mltDMembrane-bound lytic murein transglycosylase D precursor. (455 aa)
ROD_03521Conserved hypothetical protein; Belongs to the DapA family. (309 aa)
ROD_03531Hypothetical protein. (86 aa)
prpBMethylisocitrate 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. (294 aa)
prpD2-methylcitrate dehydratase. (483 aa)
hemBDelta-aminolevulinic acid dehydratase; Belongs to the ALAD family. (324 aa)
ROD_05021Putative lyase. (350 aa)
hemHFerrochelatase; Catalyzes the ferrous insertion into protoporphyrin IX. Belongs to the ferrochelatase family. (320 aa)
ROD_05391Conserved hypothetical protein; Belongs to the prolyl-tRNA editing family. YbaK/EbsC subfamily. (159 aa)
purKPhosphoribosylaminoimidazole carboxylase ATPase subunit; Catalyzes the ATP-dependent conversion of 5-aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5-carboxyaminoimidazole ribonucleotide (N5-CAIR). (355 aa)
rnaRibonuclease I; Belongs to the RNase T2 family. (264 aa)
citFCitrate lyase alpha chain. (510 aa)
citECitrate lyase beta chain; Belongs to the HpcH/HpaI aldolase family. (302 aa)
citCCitrate (pro-3S)-lyase] ligase; Acetylation of prosthetic group (2-(5''-phosphoribosyl)-3'- dephosphocoenzyme-A) of the gamma subunit of citrate lyase. (358 aa)
rlpARare lipoprotein A; Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides. (367 aa)
cobDThreonine-phosphate decarboxylase. (361 aa)
speFOrnithine decarboxylase isozyme, inducible. (732 aa)
phrBDeoxyribodipyrimidine photolyase; Belongs to the DNA photolyase family. (472 aa)
ROD_07671Putative aconitase. (754 aa)
hutUUrocanate hydratase; Catalyzes the conversion of urocanate to 4-imidazolone-5- propionate. (561 aa)
hutHHistidine ammonia-lyase. (506 aa)
moaAMolybdenum cofactor biosynthesis protein A; Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate. (329 aa)
moaCMolybdenum cofactor biosynthesis protein C; Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP); Belongs to the MoaC family. (161 aa)
fsaAFructose-6-phosphate aldolase; Catalyzes the reversible formation of fructose 6-phosphate from dihydroxyacetone and D-glyceraldehyde 3-phosphate via an aldolization reaction; Belongs to the transaldolase family. Type 3A subfamily. (220 aa)
ltaELow specificity L-threonine aldolase. (333 aa)
ROD_09311Putative phage lytic transglycosylase. (245 aa)
fabA3-hydroxydecanoyl-[acyl-carrier-protein] dehydratase; Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl-ACP to E- (2)-decenoyl-ACP and then its isomerization to Z-(3)-decenoyl-ACP. Can catalyze the dehydratase reaction for beta-hydroxyacyl-ACPs with saturated chain lengths up to 16:0, being most active on intermediate chain length. (172 aa)
mgsAMethylglyoxal synthase; Catalyzes the formation of methylglyoxal from dihydroxyacetone phosphate. (152 aa)
ROD_10731Putative peroxidase; Involved in the recovery of exogenous heme iron. Extracts iron from heme while preserving the tetrapyrrol ring intact. Belongs to the DyP-type peroxidase family. (423 aa)
pabC4-amino-4-deoxychorismate lyase. (269 aa)
mltGPutative aminodeoxychorismate lyase; Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation. (340 aa)
purBAdenylosuccinate lyase; Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily. (456 aa)
ROD_12381Putative sugar aldolase. (212 aa)
ROD_12451Putative aconitate hydratase. (882 aa)
ROD_12811Putative sugar-bisphosphate aldolase. (278 aa)
aroD3-dehydroquinate dehydratase; 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. Belongs to the type-I 3-dehydroquinase family. (252 aa)
sufSCysteine desulfurase (selenocysteine lyase); Cysteine desulfurases mobilize the sulfur from L-cysteine to yield L-alanine, an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Component of the suf operon, which is activated and required under specific conditions such as oxidative stress and iron limitation. Acts as a potent selenocysteine lyase in vitro, that mobilizes selenium from L- selenocysteine. Selenocysteine lyase activity is however unsure in vivo. (406 aa)
ROD_13791Conserved hypothetical protein. (69 aa)
gloALactoylglutathione lyase; Catalyzes the conversion of hemimercaptal, formed from methylglyoxal and glutathione, to S-lactoylglutathione. (135 aa)
nthEndonuclease III; DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N-glycosidic bond, leaving an AP (apurinic/apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'- phosphate. (211 aa)
fumAFumarate hydratase class I, aerobic; Catalyzes the reversible hydration of fumarate to (S)-malate. Belongs to the class-I fumarase family. (548 aa)
fumCFumarate hydratase class II; Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate; Belongs to the class-II fumarase/aspartase family. Fumarase subfamily. (467 aa)
dapAPutative dihydrodipicolinate synthase; Belongs to the DapA family. (294 aa)
sfcANAD-dependent malic enzyme. (565 aa)
ROD_15651Conserved hypothetical protein. (142 aa)
ROD_16291Conserved hypothetical protein. (137 aa)
pyrFOrotidine 5'-phosphate decarboxylase; Catalyzes the decarboxylation of orotidine 5'-monophosphate (OMP) to uridine 5'-monophosphate (UMP); Belongs to the OMP decarboxylase family. Type 1 subfamily. (245 aa)
acnAAconitate hydratase 1 (citrate hydro-lyase 1); Catalyzes the isomerization of citrate to isocitrate via cis- aconitate. (891 aa)
trpEAnthranilate synthase component I. (520 aa)
trpDAnthranilate synthase component II; Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'- phosphoribosyl)-anthranilate (PRA). (531 aa)
trpCTryptophan biosynthesis protein; Belongs to the TrpC family. (452 aa)
trpBTryptophan synthase beta chain; The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine. (397 aa)
trpATryptophan synthase alpha chain; The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3-phosphate. Belongs to the TrpA family. (268 aa)
chaCCation transport protein; Catalyzes the cleavage of glutathione into 5-oxo-L-proline and a Cys-Gly dipeptide. Acts specifically on glutathione, but not on other gamma-glutamyl peptides; Belongs to the gamma-glutamylcyclotransferase family. (238 aa)
mltEMembrane-bound lytic murein transglycosylase E; Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and/or cell division. Preferentially cleaves at a distance of more than two disaccharide units from the ends of the glycan chain. (203 aa)
sdaAL-serine deaminase 1; Belongs to the iron-sulfur dependent L-serine dehydratase family. (454 aa)
edaKHG/KDPG aldolase [includes: 4-hydroxy-2-oxoglutarate aldolase; 2 dehydro-3-deoxy-phosphogluconate aldolase]. (213 aa)
eddPhosphogluconate dehydratase; Catalyzes the dehydration of 6-phospho-D-gluconate to 2- dehydro-3-deoxy-6-phospho-D-gluconate; Belongs to the IlvD/Edd family. (603 aa)
dcyDD-cysteine desulfhydrase; Catalyzes the alpha,beta-elimination reaction of D-cysteine and of several D-cysteine derivatives. It could be a defense mechanism against D-cysteine; Belongs to the ACC deaminase/D-cysteine desulfhydrase family. (328 aa)
cbiKSirohydrochlorin cobaltochelatase; Catalyzes the insertion of Co(2+) into sirohydrochlorin. Belongs to the CbiK family. (264 aa)
cbiBCobalamin biosynthesis protein CbiB; Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group. (319 aa)
pduCGlycerol dehydratase large subunit. (554 aa)
pduDPropanediol utilization dehydratase, medium subunit. (222 aa)
pduEPropanediol utilization dehydratase, small subunit. (173 aa)
hisBHistidine biosynthesis bifunctional protein includes histidinol-phosphatase; imidazoleglycerol-phosphat dehydratase]. (355 aa)
hisHImidazole glycerol phosphate synthase subunit; IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the synthesis of IGP and AICAR. The resulting ammonia molecule is channeled to the active site of HisF. (196 aa)
hisFImidazole glycerol phosphate synthase subunit; IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit. (258 aa)
rfbBdTDP-glucose 4,6-dehydratase; Belongs to the NAD(P)-dependent epimerase/dehydratase family. dTDP-glucose dehydratase subfamily. (361 aa)
gmdGDP-mannose 4,6-dehydratase; Catalyzes the conversion of GDP-D-mannose to GDP-4-dehydro-6- deoxy-D-mannose. (373 aa)
ROD_22211Putative mandelate racemase/muconate lactonising enzyme. (384 aa)
fbaBFructose-bisphosphate aldolase class 1. (350 aa)
psuGConserved hypothetical protein; Catalyzes the reversible cleavage of pseudouridine 5'- phosphate (PsiMP) to ribose 5-phosphate and uracil. Functions biologically in the cleavage direction, as part of a pseudouridine degradation pathway; Belongs to the pseudouridine-5'-phosphate glycosidase family. (311 aa)
uxuAD-mannonate hydrolase; Catalyzes the dehydration of D-mannonate. (396 aa)
cysMCysteine synthase B; Belongs to the cysteine synthase/cystathionine beta- synthase family. (303 aa)
eutCEthanolamine ammonia-lyase light chain; Belongs to the EutC family. (298 aa)
eutBEthanolamine ammonia-lyase heavy chain. (453 aa)
eutAEthanolamine utilization protein. (467 aa)
maeBNADP-dependent malic enzyme. (759 aa)
dapA-2Dihydrodipicolinate synthase; Catalyzes the condensation of (S)-aspartate-beta-semialdehyde [(S)-ASA] and pyruvate to 4-hydroxy-tetrahydrodipicolinate (HTPA). (292 aa)
mltFPutative lytic transglycosylase; Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella. (515 aa)
murQN-acetylmuramic acid 6-phosphate etherase; Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6-phosphate and D- lactate. Together with AnmK, is also required for the utilization of anhydro-N-acetylmuramic acid (anhMurNAc) either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling; Belongs to the GCKR-like family. MurNAc-6-P etherase subfamily. (297 aa)
ROD_25161Conserved hypothetical protein; Belongs to the DapA family. (297 aa)
pheAP-protein. (386 aa)
ROD_25481Putative dihydrodipicolinate synthetase; Belongs to the DapA family. (306 aa)
rhmAPutative carbon-carbon lyase; Catalyzes the reversible retro-aldol cleavage of 2-keto-3- deoxy-L-rhamnonate (KDR) to pyruvate and lactaldehyde. Belongs to the HpcH/HpaI aldolase family. KDR aldolase subfamily. (267 aa)
menCO-succinylbenzoate synthase; Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB). (320 aa)
menBNaphthoate synthase; Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4-dihydroxy-2- naphthoyl-CoA (DHNA-CoA). (285 aa)
menHacyl-CoA thioester hydrolase; Catalyzes a proton abstraction reaction that results in 2,5- elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6- hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC). (252 aa)
folXD-erythro-7,8-dihydroneopterin triphosphate epimerase. (120 aa)
aroCChorismate synthase; Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system. (361 aa)
fadJFatty acid oxidation complex alpha subunit [includes: enoyl-CoA hydratase; Catalyzes the formation of a hydroxyacyl-CoA by addition of water on enoyl-CoA. Also exhibits 3-hydroxyacyl-CoA epimerase and 3- hydroxyacyl-CoA dehydrogenase activities; In the N-terminal section; belongs to the enoyl-CoA hydratase/isomerase family. (714 aa)
ROD_28081Putative decarboxylase. (551 aa)
sdaBL-serine dehydratase 2 (L-serine deaminase 2); Belongs to the iron-sulfur dependent L-serine dehydratase family. (455 aa)
fucAL-fuculose phosphate aldolase; Involved in the degradation of L-fucose and D-arabinose. Catalyzes the reversible cleavage of L-fuculose 1-phosphate (Fuc1P) to yield dihydroxyacetone phosphate (DHAP) and L-lactaldehyde. (215 aa)
mltAMembrane-bound lytic murein transglycosylase A; Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and/or cell division. (365 aa)
lysADiaminopimelate decarboxylase; Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine. (420 aa)
oglOligogalacturonate lyase. (391 aa)
gudXGlucarate dehydratase-related protein. (446 aa)
gudDGlucarate dehydratase. (446 aa)
enoEnolase; Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis. (432 aa)
queEConserved 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)
ROD_30411Putative 6-pyruvoyl tetrahydrobiopterin synthase. (120 aa)
ispF2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase; Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4-diphosphocytidyl-2- C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP). (168 aa)
ROD_30711Putative 4-hydroxybenzoate decarboxylase subunit C; Involved in the non-oxidative decarboxylation and detoxification of phenolic derivatives. (475 aa)
hypEHydrogenase isoenzymes formation protein. (322 aa)
hycAFormate hydrogenlyase regulatory protein. (153 aa)
luxSS-ribosylhomocysteinase; Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5-dihydroxy-2,3-pentadione (DPD). Belongs to the LuxS family. (171 aa)
ROD_31591Sugar bisphosphate aldolase. (286 aa)
ROD_31651Similar to Dimethylmenaquinone transferase but no experimental evidence. (237 aa)
aspAAspartate ammonia-lyase. (478 aa)
psdPhosphatidylserine decarboxylase proenzyme; Catalyzes the formation of phosphatidylethanolamine (PtdEtn) from phosphatidylserine (PtdSer). (323 aa)
nnrDPutative carbohydrate kinase; 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. Catalyzes the epimerization of the S- and R-forms of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration. This is a prerequisite for the S-specific NAD(P)H-hydrate dehydratase to allow the repair of [...] (515 aa)
ulaD3-keto-L-gulonate-6-phosphate decarboxylase (L-ascorbate utilization protein D). (217 aa)
ROD_33061Conserved hypothetical protein. (246 aa)
ROD_34021Putative diaminopropionate ammonia-lyase. (399 aa)
nrfGFormate-dependent nitrite reductase complex subunit. (202 aa)
fumBFumarate hydratase class I, anaerobic; Catalyzes the reversible hydration of fumarate to (S)-malate. Belongs to the class-I fumarase family. (548 aa)
metCCystathionine beta-lyase. (395 aa)
ribB3,4-dihydroxy-2-butanone 4-phosphate synthase; Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate. (217 aa)
ROD_36031Dihydroneopterin aldolase; Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin. (121 aa)
ttdAL-tartrate dehydratase subunit alpha. (303 aa)
ttdBL-tartrate dehydratase subunit beta. (201 aa)
ROD_36351Conserved hypothetical protein. (138 aa)
ubiCChorismate--pyruvate lyase; Removes the pyruvyl group from chorismate, with concomitant aromatization of the ring, to provide 4-hydroxybenzoate (4HB) for the ubiquinone pathway. (165 aa)
aceAIsocitrate lyase. (434 aa)
hemEUroporphyrinogen decarboxylase; Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III. (354 aa)
thiCThiamine biosynthesis protein; Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction. (631 aa)
thiHThiamine biosynthesis protein. (377 aa)
argHArgininosuccinate lyase. (457 aa)
ppcPhosphoenolpyruvate carboxylase; Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle; Belongs to the PEPCase type 1 family. (883 aa)
pflCPyruvate formate-lyase 2 activating enzyme. (292 aa)
fsaBFructose-6-phosphate aldolase 2; Catalyzes the reversible formation of fructose 6-phosphate from dihydroxyacetone and D-glyceraldehyde 3-phosphate via an aldolization reaction; Belongs to the transaldolase family. Type 3A subfamily. (220 aa)
ROD_38421Putative lyase; Belongs to the DapA family. (296 aa)
rhaDRhamnulose-1-phosphate aldolase; Catalyzes the reversible cleavage of L-rhamnulose-1-phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde. Belongs to the aldolase class II family. RhaD subfamily. (275 aa)
ROD_38801Putative sugar 1,6-diphosphate aldolase; Cleaves 6-deoxy-6-sulfo-D-fructose 1-phosphate (SFP) to form dihydroxyacetone phosphate (DHAP) and 3-sulfolactaldehyde (SLA). Belongs to the aldolase LacD family. (292 aa)
fadBFatty oxidation complex subunit alpha [includes: enoyl-CoA hydratase; Involved in the aerobic and anaerobic degradation of long- chain fatty acids via beta-oxidation cycle. Catalyzes the formation of 3-oxoacyl-CoA from enoyl-CoA via L-3-hydroxyacyl-CoA. It can also use D-3-hydroxyacyl-CoA and cis-3-enoyl-CoA as substrate. In the N-terminal section; belongs to the enoyl-CoA hydratase/isomerase family. (729 aa)
ubiD3-octaprenyl-4-hydroxybenzoate carboxy-lyase; Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol, an intermediate step in ubiquinone biosynthesis. (497 aa)
cyaAAdenylate cyclase; Belongs to the adenylyl cyclase class-1 family. (848 aa)
hemDUroporphyrinogen III synthase; Catalyzes cyclization of the linear tetrapyrrole, hydroxymethylbilane, to the macrocyclic uroporphyrinogen III. (246 aa)
rffGdTDP-glucose 4,6-dehydratase; Belongs to the NAD(P)-dependent epimerase/dehydratase family. dTDP-glucose dehydratase subfamily. (355 aa)
ilvAThreonine dehydratase biosynthetic (threonine deaminase); Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short-lived. The second step is the nonenzymatic hydrolysis of the enamine/imine intermediates to form 2- ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA. (521 aa)
ilvDDihydroxy-acid dehydratase; Belongs to the IlvD/Edd family. (616 aa)
dgoA2-dehydro-3-deoxy-6-phosphogalactonate aldolase. (205 aa)
dsdAD-serine dehydratase. (440 aa)
coaBCCoenzyme A biosynthesis bifunctional protein [includes: phosphopantothenoylcysteine decarboxylase; Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4- phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine; In the C-terminal section; belongs to the PPC synthetase family. (406 aa)
mutMformamidopyrimidine-DNA glycosylase; 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. (269 aa)
ROD_42111Putative racemase; Belongs to the mandelate racemase/muconate lactonizing enzyme family. (398 aa)
mtlRMannitol operon repressor. (195 aa)
ROD_43121Conserved hypothetical protein. (232 aa)
padCPhenolic acid decarboxylase. (168 aa)
ROD_43271Putative dehydratase. (158 aa)
ROD_43341Putative acyl carrier protein dehydratase. (117 aa)
pckAPhosphoenolpyruvate carboxykinase [ATP]; Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA. Belongs to the phosphoenolpyruvate carboxykinase (ATP) family. (539 aa)
aroB3-dehydroquinate synthase; Catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ). (362 aa)
cysGSiroheme synthase; Multifunctional enzyme that catalyzes the SAM-dependent methylations of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 via precorrin-1. Then it catalyzes the NAD-dependent ring dehydrogenation of precorrin-2 to yield sirohydrochlorin. Finally, it catalyzes the ferrochelation of sirohydrochlorin to yield siroheme. Belongs to the precorrin methyltransferase family. In the N-terminal section; belongs to the precorrin-2 dehydrogenase / sirohydrochlorin ferrochelatase family. (457 aa)
nanAN-acetylneuraminate lyase; Catalyzes the reversible aldol cleavage of N-acetylneuraminic acid (sialic acid; Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate. (297 aa)
uxuA-2Putative mannonate dehydratase; Catalyzes the dehydration of D-mannonate. (354 aa)
elbBEnhancing lycopene biosynthesis protein 2 (sigma cross-reacting protein 27A); Displays glyoxalase activity, catalyzing the conversion of glyoxal to glycolate; Belongs to the peptidase C56 family. (217 aa)
gatYTagatose-1,6-bisphosphate aldolase. (284 aa)
garDD-galactarate dehydratase; Catalyzes the dehydration of galactarate to form 5-dehydro-4- deoxy-D-glucarate. (523 aa)
garL2-dehydro-3-deoxyglucarate 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)
tdcBCatabolic threonine dehydratase; Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short-lived. The second step is the nonenzymatic hydrolysis of the enamine/imine intermediates to form 2- ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA. (329 aa)
tdcGL-serine dehydratase; Belongs to the iron-sulfur dependent L-serine dehydratase family. (454 aa)
ROD_47661Conserved hypothetical protein; Belongs to the UPF0597 family. (436 aa)
uxaAAltronate hydrolase. (495 aa)
metC-2Cystathionine beta-lyase. (396 aa)
ROD_48391Conserved hypothetical protein. (406 aa)
dgoA-22-dehydro-3-deoxy-6-phosphogalactonate aldolase. (201 aa)
deoCDeoxyribose-phosphate aldolase; Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy-D-ribose 5- phosphate; Belongs to the DeoC/FbaB aldolase family. DeoC type 2 subfamily. (259 aa)
speCOrnithine decarboxylase, constitutive. (711 aa)
mltCMembrane-bound lytic murein transglycosylase C; Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and/or cell division. (360 aa)
speABiosynthetic arginine decarboxylase; Catalyzes the biosynthesis of agmatine from arginine. (658 aa)
fbaAFructose-bisphosphate aldolase class 2; 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; Belongs to the class II fructose-bisphosphate aldolase family. (359 aa)
sltSoluble lytic murein transglycosylase precursor. (645 aa)
Your Current Organism:
Citrobacter rodentium
NCBI taxonomy Id: 637910
Other names: C. rodentium ICC168, Citrobacter rodentium ICC168, Citrobacter rodentium str. ICC168, Citrobacter rodentium strain ICC168
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