STRINGSTRING
proB proB tnaA tnaA tssA2 tssA2 tssA1 tssA1 act1 act1 argF argF argE argE argD argD argC argC argX argX argW argW argH argH argG argG glyS glyS panE panE hemD hemD sufS1 sufS1 HVO_0113 HVO_0113 serA1 serA1 tyrS tyrS hisG hisG HVO_0189 HVO_0189 alaS1 alaS1 guaAa2 guaAa2 acd1 acd1 HVO_0212 HVO_0212 HVO_0214 HVO_0214 glnA glnA ltaE ltaE etfA1 etfA1 argS argS ilvE ilvE fadM1 fadM1 hom1 hom1 HVO_0419 HVO_0419 hisE hisE pdxT pdxT HVO_0441 HVO_0441 hisH hisH pheA pheA leuS leuS ala ala ilvA1 ilvA1 thrC1 thrC1 gap1 gap1 pgk pgk gap2 gap2 HVO_0483 HVO_0483 guaAa3 guaAa3 mptD mptD HVO_0586 HVO_0586 cobD1 cobD1 cobD2 cobD2 hom2 hom2 aroD1 aroD1 aroD2 aroD2 HVO_0608 HVO_0608 HVO_0609 HVO_0609 HVO_0613 HVO_0613 leuA1 leuA1 guaAa1 guaAa1 dsa2 dsa2 oadhB3 oadhB3 oadhA3 oadhA3 aspS aspS HVO_0687 HVO_0687 pabC pabC pabB pabB aroE2 aroE2 aroE1 aroE1 dtdA dtdA HVO_0771 HVO_0771 trpC trpC trpB trpB trpA trpA fba2 fba2 aroB aroB pykA pykA metS metS panD panD ppsA ppsA thrC2 thrC2 mmcB mmcB acaB1 acaB1 HVO_0866 HVO_0866 gltB gltB proS proS HVO_0880 HVO_0880 nosD nosD mmcA1 mmcA1 acs1 acs1 HVO_0914 HVO_0914 fdhA fdhA aspC3 aspC3 acaB2 acaB2 HVO_1039 HVO_1039 HVO_1041 HVO_1041 hisF hisF asnB asnB gatC gatC coaBC coaBC HVO_1073 HVO_1073 folCP folCP dapE dapE dapF dapF lysA lysA dapD dapD dapB dapB dapA dapA cysS cysS acd2 acd2 aldH2 aldH2 fadM2 fadM2 acd3 acd3 acs3 acs3 hdrA hdrA HVO_1291 HVO_1291 hisC hisC tpiA1 tpiA1 aroC aroC aroA aroA tyrA tyrA aroQ aroQ aroK aroK HVO_1368 HVO_1368 proA proA proC proC acd4 acd4 acs4 acs4 mmcA2 mmcA2 fadA1 fadA1 HVO_1395 HVO_1395 HVO_1415 HVO_1415 cysK1 cysK1 hbd3 hbd3 pccB1 pccB1 maoC1 maoC1 gdhA1 gdhA1 citE citE gdhA2 gdhA2 pyrB pyrB fadA2 fadA2 menF menF gnaD gnaD fba1 fba1 leuB leuB leuD1 leuD1 leuC1 leuC1 ilvC ilvC ilvN ilvN leuA2 leuA2 aglM aglM ileS ileS act2 act2 aspC1 aspC1 cysK2 cysK2 thrS thrS HVO_1693 HVO_1693 HVO_1697 HVO_1697 HVO_1699 HVO_1699 HVO_1784 HVO_1784 gndA gndA hisS hisS lysS lysS HVO_1875 HVO_1875 fadA3 fadA3 HVO_1905 HVO_1905 acaB3 acaB3 acs6 acs6 serS serS ddh ddh cofE cofE pdaD pdaD pgi pgi aceB1 aceB1 aceA aceA cysE cysE HVO_2091 HVO_2091 tpiA2 tpiA2 HVO_2106 HVO_2106 HVO_2114 HVO_2114 HVO_2127 HVO_2127 amaB1 amaB1 maeB1 maeB1 purQ purQ cofC cofC oadhA4 oadhA4 trpD2 trpD2 HVO_2244 HVO_2244 speB speB thrB thrB HVO_2360 HVO_2360 carB carB HVO_2370 HVO_2370 hadL hadL gcvP2 gcvP2 gcvP1 gcvP1 gcvH gcvH gcvT gcvT maeB2 maeB2 trpG trpG trpE trpE trpF trpF trpD1 trpD1 pccB2 pccB2 cofD cofD asd asd kynU kynU carA carA gatD gatD gpmI gpmI nadC nadC nadA nadA HVO_2582 HVO_2582 icd icd oadhA2 oadhA2 oadhB2 oadhB2 ppc ppc maa maa pyrG pyrG HVO_2638 HVO_2638 ilvD ilvD serA2 serA2 HVO_2661 HVO_2661 HVO_2665 HVO_2665 HVO_2671 HVO_2671 hisD hisD panB2 panB2 tif2Bd tif2Bd acd5 acd5 alaS2 alaS2 purF purF gltS gltS HVO_2727 HVO_2727 etfA2 etfA2 metE1 metE1 metE2 metE2 metB1 metB1 eno eno hbd1 hbd1 glyA1 glyA1 folD folD HVO_2871 HVO_2871 HVO_2879 HVO_2879 fumC fumC maoC3 maoC3 folP2 folP2 mptE mptE HVO_2917 HVO_2917 hdrB hdrB HVO_2926 HVO_2926 valS valS metB2 metB2 pheT pheT pheS pheS ocd3 ocd3 trpS1 trpS1 lipA lipA oadhA1 oadhA1 oadhB1 oadhB1 lpdA lpdA serB serB thrC3 thrC3 hisB hisB hisA hisA hisI hisI metY2 metY2 metX metX metY1 metY1 mdh mdh
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proBGlutamate 5-kinase; Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate. (301 aa)
tnaATryptophanase. (448 aa)
tssA2Thiosulfate sulfurtransferase. (258 aa)
tssA1Thiosulfate sulfurtransferase; May be a sulfotransferase involved in the formation of thiosulfate. (286 aa)
act1acyl-CoA thioester hydrolase. (164 aa)
argFOrnithine carbamoyltransferase; Belongs to the aspartate/ornithine carbamoyltransferase superfamily. OTCase family. (299 aa)
argEAcetylornithine deacetylase; Catalyzes the release of L-lysine from [LysW]-gamma-L-lysine and the release of L-ornithine from [LysW]-L-ornithine. (381 aa)
argDAcetylornithine aminotransferase; Involved in both the arginine and lysine biosynthetic pathways; Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. LysJ subfamily. (378 aa)
argCN-acetyl-gamma-glutamyl-phosphate reductase; Involved in both the arginine and lysine biosynthetic pathways; Belongs to the NAGSA dehydrogenase family. Type 1 subfamily. LysY sub-subfamily. (347 aa)
argXPutative glutamate--argW ligase. (291 aa)
argWPutative biosynthetic carrier protein ArgW. (59 aa)
argHArgininosuccinate lyase. (488 aa)
argGArgininosuccinate synthase; Belongs to the argininosuccinate synthase family. Type 1 subfamily. (405 aa)
glySglycine--tRNA ligase. (594 aa)
panE2-dehydropantoate 2-reductase; Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid. (298 aa)
hemDuroporphyrinogen-III synthase. (247 aa)
sufS1Cysteine desulfurase; Catalyzes the removal of elemental sulfur atoms from cysteine to produce alanine. Able to reassemble a removed [2Fe-2S] cluster of an apo-ferredoxin. Shows a selenocysteine lyase activity approximately 280-fold higher than its cysteine desulfurase activity. Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. Csd subfamily. (426 aa)
HVO_0113Putative phosphatase (histidine phosphatase family protein). (205 aa)
serA1Putative D-2-hydroxyacid dehydrogenase; Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. (324 aa)
tyrStyrosine--tRNA ligase; 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); Belongs to the class-I aminoacyl-tRNA synthetase family. TyrS type 3 subfamily. (328 aa)
hisGATP 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. Belongs to the ATP phosphoribosyltransferase family. Long subfamily. (281 aa)
HVO_0189CobC/GpmA family phosphatase. (212 aa)
alaS1alanine--tRNA ligase; 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. (922 aa)
guaAa2Glutamine amidotransferase (homolog to GMP synthase subunit A). (237 aa)
acd1glutaryl-CoA dehydrogenase. (387 aa)
HVO_0212Glyoxalase domain protein. (124 aa)
HVO_0214L-lactate dehydrogenase; Belongs to the LDH/MDH superfamily. (320 aa)
glnAGlutamine synthetase; Glutamine synthetase (GS) is an unusual multitasking protein that functions as an enzyme, a transcription coregulator, and a chaperone in ammonium assimilation and in the regulation of genes involved in nitrogen metabolism. It catalyzes the ATP-dependent biosynthesis of glutamine from glutamate and ammonia. Feedback- inhibited GlnA also interacts with and regulates the activity of the transcriptional regulator TnrA. During nitrogen limitation, TnrA is in its DNA-binding active state and turns on the transcription of genes required for nitrogen assimilation. Under [...] (456 aa)
ltaEThreonine aldolase. (341 aa)
etfA1Electron transfer flavoprotein alpha subunit. (317 aa)
argSarginine--tRNA ligase; Belongs to the class-I aminoacyl-tRNA synthetase family. (587 aa)
ilvEBranched-chain amino acid aminotransferase; Acts on leucine, isoleucine and valine. Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family. (312 aa)
fadM1Proline dehydrogenase. (279 aa)
hom1Homoserine dehydrogenase. (317 aa)
HVO_0419Peptidase M20 family protein (homolog to succinyl-diaminopimelate desuccinylase). (364 aa)
hisEphosphoribosyl-ATP pyrophosphatase. (100 aa)
pdxTPyridoxal 5'-phosphate synthase subunit PdxT; 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. (202 aa)
HVO_0441Beta-lactamase domain protein. (208 aa)
hisHImidazoleglycerol-phosphate synthase subunit HisH; 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. (219 aa)
pheAPrephenate dehydratase. (268 aa)
leuSleucine--tRNA ligase; Belongs to the class-I aminoacyl-tRNA synthetase family. (958 aa)
alaAlanine dehydrogenase; Catalyzes the NAD(+)-dependent oxidative deamination of L- alanine to pyruvate, and the reverse reaction, the reductive amination of pyruvate; Belongs to the ornithine cyclodeaminase/mu-crystallin family. Archaeal alanine dehydrogenase subfamily. (331 aa)
ilvA1Threonine ammonia-lyase. (403 aa)
thrC1Threonine synthase. (367 aa)
gap1Glyceraldehyde-3-phosphate dehydrogenase (NAD(P)) (phosphorylating). (355 aa)
pgkPhosphoglycerate kinase; Belongs to the phosphoglycerate kinase family. (401 aa)
gap2Glyceraldehyde-3-phosphate dehydrogenase (NAD) (phosphorylating); Belongs to the glyceraldehyde-3-phosphate dehydrogenase family. (350 aa)
HVO_0483ATP-grasp fold protein. (290 aa)
guaAa3Glutamine amidotransferase (homolog to GMP synthase subunit A). (215 aa)
mptDDihydroneopterin aldolase, archaeal-type; Catalyzes the conversion of 7,8-dihydroneopterin (H2Neo) to 6-hydroxymethyl-7,8-dihydropterin (6-HMD); Belongs to the archaeal dihydroneopterin aldolase family. (113 aa)
HVO_0586HAD superfamily hydrolase. (211 aa)
cobD1L-threonine-O-3-phosphate decarboxylase. (340 aa)
cobD2L-threonine-O-3-phosphate decarboxylase. (337 aa)
hom2Homoserine dehydrogenase. (316 aa)
aroD13-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. (247 aa)
aroD23-dehydroquinate dehydratase. (222 aa)
HVO_0608Oxidoreductase (homolog to zinc-containing alcohol dehydrogenase). (347 aa)
HVO_0609Beta-lactamase domain protein. (215 aa)
HVO_0613Beta-lactamase domain protein. (215 aa)
leuA12-isopropylmalate synthase / (R)-citramalate synthase; Belongs to the alpha-IPM synthase/homocitrate synthase family. (512 aa)
guaAa1GMP synthase (glutamine-hydrolyzing) subunit A; Catalyzes the synthesis of GMP from XMP. (183 aa)
dsa2Dihydrolipoamide S-acyltransferase. (495 aa)
oadhB32-oxoacid dehydrogenase E1 component beta subunit. (336 aa)
oadhA32-oxoacid dehydrogenase E1 component alpha subunit. (344 aa)
aspSaspartate--tRNA(Asp/Asn) ligase; 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). (434 aa)
HVO_0687M20 family amidohydrolase; Belongs to the peptidase M20A family. (444 aa)
pabCAminodeoxychorismate lyase; Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family. (330 aa)
pabBAminodeoxychorismate synthase component 1. (504 aa)
aroE2Shikimate 5-dehydrogenase C-terminal domain protein. (157 aa)
aroE1Shikimate 5-dehydrogenase N-terminal domain protein. (121 aa)
dtdAD-aminoacyl-tRNA deacylase; D-aminoacyl-tRNA deacylase with broad substrate specificity. 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. (439 aa)
HVO_0771Beta-lactamase domain protein. (262 aa)
trpCIndole-3-glycerol-phosphate synthase; Belongs to the TrpC family. (251 aa)
trpBTryptophan synthase beta subunit; The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine. (422 aa)
trpATryptophan synthase alpha subunit; The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3-phosphate. (277 aa)
fba22-amino-3,7-dideoxy-D-threo-hept-6-ulosonate synthase; Catalyzes a transaldol reaction between 6-deoxy-5- ketofructose 1-phosphate (DKFP) and L-aspartate semialdehyde (ASA) with an elimination of hydroxypyruvaldehyde phosphate to yield 2-amino-3,7- dideoxy-D-threo-hept-6-ulosonate (ADH). Plays a key role in an alternative pathway of the biosynthesis of 3-dehydroquinate (DHQ), which is involved in the canonical pathway for the biosynthesis of aromatic amino acids. (266 aa)
aroB3-dehydroquinate synthase, type II; Catalyzes the oxidative deamination and cyclization of 2- amino-3,7-dideoxy-D-threo-hept-6-ulosonic acid (ADH) to yield 3- dehydroquinate (DHQ), which is fed into the canonical shikimic pathway of aromatic amino acid biosynthesis; Belongs to the archaeal-type DHQ synthase family. (392 aa)
pykAPyruvate kinase; Belongs to the pyruvate kinase family. (585 aa)
metSmethionine--tRNA ligase; Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation. (740 aa)
panDAspartate 1-decarboxylase; Catalyzes the decarboxylation of L-aspartate to produce beta- alanine; Belongs to the group II decarboxylase family. MfnA subfamily. (357 aa)
ppsAPhosphoenolpyruvate synthase; Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate; Belongs to the PEP-utilizing enzyme family. (761 aa)
thrC2Threonine synthase. (389 aa)
mmcBmethylmalonyl-CoA mutase subunit B (cobalamin-binding subunit). (139 aa)
acaB1acetyl-CoA C-acetyltransferase. (388 aa)
HVO_0866Homolog to alanine-tRNA ligase. (244 aa)
gltBGlutamate synthase large subunit. (1511 aa)
proSproline--tRNA ligase; 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). (488 aa)
HVO_0880Uncharacterized protein; COG 1340. (307 aa)
nosDABC-type transport system periplasmic substrate-binding protein (probable substrate copper). (641 aa)
mmcA1methylmalonyl-CoA mutase subunit A. (566 aa)
acs1acyl-CoA synthetase. (662 aa)
HVO_0914Glyoxalase domain protein. (259 aa)
fdhAFormate dehydrogenase alpha subunit. (680 aa)
aspC3Pyridoxal phosphate-dependent aminotransferase (probable aspartate aminotransferase). (384 aa)
acaB2acetyl-CoA C-acetyltransferase catalytic subunit. (383 aa)
HVO_1039Metallo-beta-lactamase superfamily protein. (167 aa)
HVO_1041Beta-lactamase domain protein. (332 aa)
hisFImidazoleglycerol-phosphate synthase subunit HisF; 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. (270 aa)
asnBAsparagine synthase (glutamine-hydrolyzing). (363 aa)
gatCaspartyl/glutamyl-tRNA(Asn/Gln) amidotransferase subunit C; Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp-tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl- tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp- tRNA(Asn) or phospho-Glu-tRNA(Gln); Belongs to the GatC family. (92 aa)
coaBCPhosphopantothenoylcysteine decarboxylase / phosphopantothenate--cysteine ligase. (386 aa)
HVO_1073ThiJ/PfpI domain protein. (224 aa)
folCPFolylpolyglutamate synthase / 7,8-dihydropteroate reductase / dihydropteroate synthase; Can complement an H.volcanii mutant strain that is thymidine auxotroph because it lacks the two dihydrofolate reductase genes encoded by hdrA and hdrB; In the N-terminal section; belongs to the folylpolyglutamate synthase family. (838 aa)
dapESuccinyl-diaminopimelate desuccinylase. (365 aa)
dapFDiaminopimelate epimerase; Catalyzes the stereoinversion of LL-2,6-diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso-DAP), a precursor of L- lysine. (288 aa)
lysADiaminopimelate decarboxylase; Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine. (415 aa)
dapD2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase. (280 aa)
dapB4-hydroxy-tetrahydrodipicolinate reductase; Catalyzes the conversion of 4-hydroxy-tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate; Belongs to the DapB family. (253 aa)
dapA4-hydroxy-tetrahydrodipicolinate synthase; Catalyzes the condensation of (S)-aspartate-beta-semialdehyde [(S)-ASA] and pyruvate to 4-hydroxy-tetrahydrodipicolinate (HTPA). (305 aa)
cysScysteine--tRNA ligase. (494 aa)
acd2acyl-CoA dehydrogenase. (380 aa)
aldH2Aldehyde dehydrogenase. (508 aa)
fadM2Proline dehydrogenase. (279 aa)
acd3acyl-CoA dehydrogenase. (380 aa)
acs3acyl-CoA synthetase. (535 aa)
hdrADihydrofolate reductase; Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis; Belongs to the dihydrofolate reductase family. (162 aa)
HVO_1291Fumarylacetoacetase family protein. (243 aa)
hisCHistidinol-phosphate aminotransferase. (361 aa)
tpiA1Triosephosphate isomerase; Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D- glyceraldehyde-3-phosphate (G3P); Belongs to the triosephosphate isomerase family. (214 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. (385 aa)
aroA3-phosphoshikimate 1-carboxyvinyltransferase; Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3-phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate. (430 aa)
tyrAPrephenate dehydrogenase. (272 aa)
aroQChorismate mutase. (103 aa)
aroKShikimate kinase, archaeal-type. (289 aa)
HVO_1368Beta-lactamase domain protein. (267 aa)
proAGamma-glutamyl phosphate reductase; Catalyzes the NADPH-dependent reduction of L-glutamate 5- phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5-carboxylate. Belongs to the gamma-glutamyl phosphate reductase family. (444 aa)
proCPyrroline-5-carboxylate reductase; Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline. (257 aa)
acd4acyl-CoA dehydrogenase. (383 aa)
acs4acyl-CoA synthetase. (553 aa)
mmcA2methylmalonyl-CoA mutase subunit A. (558 aa)
fadA1enoyl-CoA hydratase; Belongs to the enoyl-CoA hydratase/isomerase family. (257 aa)
HVO_1395M20 family amidohydrolase (homolog to indole-3-acetyl-aspartate hydrolase). (427 aa)
HVO_1415HAD superfamily hydrolase. (230 aa)
cysK1Cysteine synthase. (326 aa)
hbd33-hydroxyacyl-CoA dehydrogenase. (286 aa)
pccB1propionyl-CoA carboxylase carboxyltransferase component. (581 aa)
maoC1MaoC domain protein. (156 aa)
gdhA1Glutamate dehydrogenase (NAD); Belongs to the Glu/Leu/Phe/Val dehydrogenases family. (428 aa)
citEHomolog to citrate lyase beta subunit. (279 aa)
gdhA2Glutamate dehydrogenase (NADP); Belongs to the Glu/Leu/Phe/Val dehydrogenases family. (417 aa)
pyrBAspartate carbamoyltransferase catalytic subunit. (304 aa)
fadA2enoyl-CoA hydratase; Belongs to the enoyl-CoA hydratase/isomerase family. (269 aa)
menFIsochorismate synthase. (443 aa)
gnaDD-gluconate dehydratase; NADP-dependent D-xylose dehydrogenase involved in the degradation of D-xylose, a major component of hemicelluloses such as xylan. Catalyzes the third reaction in the xylose utilization pathway through dehydratation of D-xylonate into 2-dehydro-3-deoxy-D-xylonate. (412 aa)
fba1Fructose-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. Is required for the utilization of fructose as a sole carbon and energy source. Plays a role in gluconeogenesis during growth on acetate, D-xylose, and casamino acids. (330 aa)
leuB3-isopropylmalate dehydrogenase; Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate. (324 aa)
leuD13-isopropylmalate dehydratase small subunit. (202 aa)
leuC13-isopropylmalate dehydratase large subunit; Catalyzes the isomerization between 2-isopropylmalate and 3- isopropylmalate, via the formation of 2-isopropylmaleate. (473 aa)
ilvCKetol-acid reductoisomerase; 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. (348 aa)
ilvNAcetolactate synthase small subunit. (218 aa)
leuA22-isopropylmalate synthase; Belongs to the alpha-IPM synthase/homocitrate synthase family. (440 aa)
aglMUDP-glucose 6-dehydrogenase AglM; Involved in the assembly of a N-linked pentasaccharide that decorates the S-layer glycoprotein and flagellins. Involved in the biosynthesis of the hexuronic acids found at both positions 2 and 3 of the pentasaccharide; Belongs to the UDP-glucose/GDP-mannose dehydrogenase family. (430 aa)
ileSisoleucine--tRNA ligase; 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). Belongs to the class-I aminoacyl-tRNA synthetase family. IleS type 2 subfamily. (1043 aa)
act2acyl-CoA thioester hydrolase. (160 aa)
aspC1Pyridoxal phosphate-dependent aminotransferase (probable aspartate aminotransferase). (373 aa)
cysK2Cysteine synthase. (306 aa)
thrSthreonine--tRNA ligase; Belongs to the class-II aminoacyl-tRNA synthetase family. (643 aa)
HVO_1693DUF162 family protein. (167 aa)
HVO_1697FAD-dependent oxidoreductase (GlcD/DLD_GlcF/GlpC domain fusion protein). (1026 aa)
HVO_1699Aminotransferase; Pyridoxal phosphate-dependent aminotransferase (homolog to histidinol-phosphate aminotransferase / aspartate aminotransferase). (378 aa)
HVO_1784Peptidase M20 family protein. (414 aa)
gndA6-phosphogluconate dehydrogenase (NAD-dependent, decarboxylating); Catalyzes the oxidative decarboxylation of 6-phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NAD to NADH. (299 aa)
hisShistidine--tRNA ligase; Belongs to the class-II aminoacyl-tRNA synthetase family. (431 aa)
lysSlysine--tRNA ligase; Belongs to the class-I aminoacyl-tRNA synthetase family. (555 aa)
HVO_1875O-acetyltransferase (homolog to galactoside O-acetyltransferase). (305 aa)
fadA3enoyl-CoA hydratase; Belongs to the enoyl-CoA hydratase/isomerase family. (231 aa)
HVO_1905Beta-lactamase domain protein. (274 aa)
acaB3acetyl-CoA C-acyltransferase. (377 aa)
acs6acyl-CoA synthetase. (666 aa)
serSserine--tRNA ligase; 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). (460 aa)
ddh2-D-hydroxyacid dehydrogenase. (308 aa)
cofECoenzyme F420:L-glutamate ligase; Catalyzes the GTP-dependent successive addition of two or more gamma-linked L-glutamates to the L-lactyl phosphodiester of 7,8- didemethyl-8-hydroxy-5-deazariboflavin (F420-0) to form coenzyme F420- 0-glutamyl-glutamate (F420-2) or polyglutamated F420 derivatives. (251 aa)
pdaDPyruvoyl-dependent arginine decarboxylase. (157 aa)
pgiGlucose-6-phosphate isomerase; Belongs to the GPI family. (430 aa)
aceB1Malate synthase; Involved in the glyoxylate cycle which synthesizes precursors for carbohydrates from C2 compounds such as acetate. Catalyzes the Claisen condensation between acetyl-coenzyme A (acetyl-CoA) and glyoxylate to form the malyl-CoA intermediate that is subsequently hydrolyzed to produce malate and CoA. (433 aa)
aceAIsocitrate lyase; Involved in the metabolic adaptation in response to environmental changes. Catalyzes the reversible formation of succinate and glyoxylate from isocitrate, a key step of the glyoxylate cycle, which operates as an anaplerotic route for replenishing the tricarboxylic acid cycle during growth on fatty acid substrates. (345 aa)
cysESerine O-acetyltransferase. (287 aa)
HVO_2091Pyridoxal phosphate-dependent aminotransferase; Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. (441 aa)
tpiA2Triosephosphate isomerase. (225 aa)
HVO_2106DeoC family aldolase. (258 aa)
HVO_2114Homolog to 4-hydroxy-tetrahydrodipicolinate synthase. (311 aa)
HVO_2127M20 family amidohydrolase (homolog to indole-3-acetyl-aspartate hydrolase). (420 aa)
amaB1Amidase (hydantoinase/carbamoylase family). (418 aa)
maeB1Malic enzyme (NADP). (751 aa)
purQPhosphoribosylformylglycinamidine synthase subunit PurQ; Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP- dependent manner. PurS interacts with PurQ and PurL and is thought [...] (224 aa)
cofC2-phospho-L-lactate guanylyltransferase; Guanylyltransferase that catalyzes the activation of phosphoenolpyruvate (PEP) as enolpyruvoyl-2-diphospho-5'-guanosine, via the condensation of PEP with GTP. It is involved in the biosynthesis of coenzyme F420, a hydride carrier cofactor; Belongs to the CofC family. (206 aa)
oadhA4Putative branched-chain amino acid dehydrogenase E1 component alpha subunit. (348 aa)
trpD2Putative phosphoribosyltransferase (homolog to anthranilate phosphoribosyltransferase). (360 aa)
HVO_2244Fumarylacetoacetase family protein. (239 aa)
speBAgmatinase; Belongs to the arginase family. (271 aa)
thrBHomoserine kinase; Catalyzes the ATP-dependent phosphorylation of L-homoserine to L-homoserine phosphate; Belongs to the GHMP kinase family. Homoserine kinase subfamily. (293 aa)
HVO_2360Peptidase S66 family protein. (340 aa)
carBCarbamoyl-phosphate synthase (glutamine-hydrolyzing) large subunit; Belongs to the CarB family. (1082 aa)
HVO_2370HAD superfamily hydrolase. (219 aa)
hadLHaloacid dehalogenase, type II. (234 aa)
gcvP2Glycine cleavage system protein P beta subunit. (473 aa)
gcvP1Glycine cleavage system protein P alpha subunit. (447 aa)
gcvHGlycine cleavage system protein H; 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. (126 aa)
gcvTGlycine cleavage system protein T; The glycine cleavage system catalyzes the degradation of glycine. (363 aa)
maeB2Malate dehydrogenase (oxaloacetate-decarboxylating). (751 aa)
trpGAnthranilate synthase component 2; Part of a heterotetrameric complex that catalyzes the two- step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine-binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentr [...] (204 aa)
trpEAnthranilate synthase component 1; Part of a heterotetrameric complex that catalyzes the two- step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine-binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentr [...] (524 aa)
trpFN-(5'-phosphoribosyl)anthranilate isomerase; Belongs to the TrpF family. (221 aa)
trpD1Anthranilate phosphoribosyltransferase; Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'- phosphoribosyl)-anthranilate (PRA). (331 aa)
pccB2propionyl-CoA carboxylase carboxyltransferase component. (516 aa)
cofD2-phospho-L-lactate transferase; Catalyzes the transfer of the phosphoenolpyruvate moiety from enoylpyruvoyl-2-diphospho-5'-guanosine (EPPG) to 7,8-didemethyl-8- hydroxy-5-deazariboflavin (FO) with the formation of dehydro coenzyme F420-0 and GMP. (330 aa)
asdAspartate-semialdehyde dehydrogenase. (344 aa)
kynUKynureninase; Catalyzes the cleavage of L-kynurenine (L-Kyn) and L-3- hydroxykynurenine (L-3OHKyn) into anthranilic acid (AA) and 3- hydroxyanthranilic acid (3-OHAA), respectively. (425 aa)
carACarbamoyl-phosphate synthase (glutamine-hydrolyzing) small subunit; Belongs to the CarA family. (360 aa)
gatDglutamyl-tRNA(Gln) amidotransferase subunit D; Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu- tRNA(Gln). The GatDE system is specific for glutamate and does not act on aspartate. (415 aa)
gpmIPhosphoglycerate mutase, 2,3-biphosphateglycerate-independent type; Catalyzes the interconversion of 2-phosphoglycerate and 3- phosphoglycerate; Belongs to the BPG-independent phosphoglycerate mutase family. (526 aa)
nadCNicotinate-nucleotide pyrophosphorylase (carboxylating); Involved in the catabolism of quinolinic acid (QA). Belongs to the NadC/ModD family. (268 aa)
nadAQuinolinate synthase A; Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate. (385 aa)
HVO_2582Metal dependent amidohydrolase M38 superfamily protein. (193 aa)
icdIsocitrate dehydrogenase (NADP); Belongs to the isocitrate and isopropylmalate dehydrogenases family. (419 aa)
oadhA22-oxoacid dehydrogenase E1 component alpha subunit. (353 aa)
oadhB22-oxoacid dehydrogenase E1 component beta subunit. (346 aa)
ppcPhosphoenolpyruvate carboxylase. (897 aa)
maaMaltose O-acetyltransferase. (185 aa)
pyrGCTP synthase; 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. (549 aa)
HVO_2638Homolog to dipeptide epimerase. (345 aa)
ilvDDihydroxy-acid dehydratase; Belongs to the IlvD/Edd family. (584 aa)
serA2Putative D-2-hydroxyacid dehydrogenase; Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. (319 aa)
HVO_2661Aminotransferase class V (serine--pyruvate aminotransferase / alanine--glyoxylate aminotransferase). (370 aa)
HVO_2665HpcH/HpaI aldolase family protein. (265 aa)
HVO_2671Aminotransferase class V (serine--pyruvate aminotransferase / alanine--glyoxylate aminotransferase). (395 aa)
hisDHistidinol dehydrogenase; Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine. (428 aa)
panB23-methyl-2-oxobutanoate hydroxymethyltransferase; Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha- ketoisovalerate to form ketopantoate; Belongs to the PanB family. (269 aa)
tif2BdTranslation initiation factor aIF-2B delta subunit; Belongs to the eIF-2B alpha/beta/delta subunits family. (282 aa)
acd5acyl-CoA dehydrogenase. (381 aa)
alaS2alanine--tRNA ligase. (398 aa)
purFAmidophosphoribosyltransferase; Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine. (493 aa)
gltSglutamate--tRNA(Glu/Gln) ligase; 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). (585 aa)
HVO_2727Cyclase family protein. (219 aa)
etfA2Electron transfer flavoprotein alpha subunit. (582 aa)
metE15-methyltetrahydropteroyltriglutamate-- homocysteine S-methyltransferase (methionine synthase II); Catalyzes the transfer of a methyl group to L-homocysteine resulting in methionine formation. The physiological methyl donor is unknown. (357 aa)
metE25-methyltetrahydropteroyltriglutamate-- homocysteine S-methyltransferase (methionine synthase II). (336 aa)
metB1Cystathionine synthase/lyase (cystathionine gamma-synthase, cystathionine gamma-lyase, cystathionine beta-lyase). (386 aa)
enoEnolase; Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis; Belongs to the enolase family. (399 aa)
hbd13-hydroxyacyl-CoA dehydrogenase / enoyl-CoA hydratase; Belongs to the enoyl-CoA hydratase/isomerase family. (661 aa)
glyA1Serine hydroxymethyltransferase; Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. Also exhibits THF-independent aldolase activity toward beta- hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism. (415 aa)
folDMethylenetetrahydrofolate dehydrogenase / methenyltetrahydrofolate cyclohydrolase; Catalyzes the oxidation of 5,10-methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10- methenyltetrahydrofolate to 10-formyltetrahydrofolate. (297 aa)
HVO_2871Pyridoxal phosphate-dependent aminotransferase; Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. (450 aa)
HVO_2879Homolog to ornithine cyclodeaminase. (332 aa)
fumCFumarate hydratase; Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate; Belongs to the class-II fumarase/aspartase family. Fumarase subfamily. (469 aa)
maoC3MaoC domain protein. (153 aa)
folP2Dihydropteroate synthase. (379 aa)
mptE6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase MptE; Catalyzes the transfer of diphosphate from ATP to 6- hydroxymethyl-7,8-dihydropterin (6-HMD), leading to 6-hydroxymethyl- 7,8-dihydropterin diphosphate (6-HMDP); Belongs to the archaeal 6-HMPDK family. (227 aa)
HVO_2917Beta-lactamase domain protein. (192 aa)
hdrBDihydrofolate reductase; Belongs to the dihydrofolate reductase family. (194 aa)
HVO_2926Metal-dependent amidohydrolase M38 superfamily protein. (253 aa)
valSvaline--tRNA ligase; 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; Belongs to the class-I aminoacyl-tRNA synthetase family. ValS type 2 subfamily. (870 aa)
metB2Cystathionine synthase/lyase (cystathionine gamma-synthase, cystathionine gamma-lyase, cystathionine beta-lyase). (401 aa)
pheTphenylalanine--tRNA ligase beta subunit. (570 aa)
pheSphenylalanine--tRNA ligase alpha subunit. (499 aa)
ocd3Ornithine cyclodeaminase. (349 aa)
trpS1tryptophan--tRNA ligase; Catalyzes the attachment of tryptophan to tRNA(Trp). (529 aa)
lipALipoate synthase; 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. (311 aa)
oadhA12-oxo-3-methylvalerate dehydrogenase E1 component alpha subunit. (368 aa)
oadhB12-oxo-3-methylvalerate dehydrogenase E1 component beta subunit. (327 aa)
lpdADihydrolipoyl dehydrogenase. (475 aa)
serBPhosphoserine phosphatase. (215 aa)
thrC3Threonine synthase; Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine. (419 aa)
hisBImidazoleglycerol-phosphate dehydratase. (197 aa)
hisA1-(5-phosphoribosyl)-5-[(5- phosphoribosylamino)methylideneamino] imidazole-4-carboxamide isomerase. (238 aa)
hisIphosphoribosyl-AMP cyclohydrolase; Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP. (122 aa)
metY2O-acetylhomoserine aminocarboxypropyltransferase (methionine synthase). (431 aa)
metXHomoserine O-acetyltransferase; Transfers an acetyl group from acetyl-CoA to L-homoserine, forming acetyl-L-homoserine. (415 aa)
metY1O-acetylhomoserine aminocarboxypropyltransferase (methionine synthase). (439 aa)
mdhMalate dehydrogenase; Catalyzes the reversible oxidation of malate to oxaloacetate. Belongs to the LDH/MDH superfamily. (304 aa)
Your Current Organism:
Haloferax volcanii
NCBI taxonomy Id: 309800
Other names: H. volcanii DS2, Haloferax volcanii ATCC 29605, Haloferax volcanii DS2, Haloferax volcanii DSM 3757, Haloferax volcanii str. DS2, Haloferax volcanii strain DS2
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