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badB | Ferredoxin. (81 aa) | ||||
fixG, | 4Fe-4S ferredoxin, iron-sulfur binding domain. (485 aa) | ||||
RPA0042 | Possible iron-sulfur cluster binding protein. (370 aa) | ||||
hydC | Hydrogenase gamma-fused hydrogenase large and small subunit. (619 aa) | ||||
RPA0135 | Possible oxidoreductase. (673 aa) | ||||
acnA | Aconitate hydratase; Catalyzes the isomerization of citrate to isocitrate via cis- aconitate. (905 aa) | ||||
sdhB | Succinate dehydrogenase iron-sulfur protein subunit; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the succinate dehydrogenase/fumarate reductase iron-sulfur protein family. (260 aa) | ||||
leuC | 3-isopropylmalate dehydratase; Catalyzes the isomerization between 2-isopropylmalate and 3- isopropylmalate, via the formation of 2-isopropylmaleate. (469 aa) | ||||
RPA0251 | MiaB-like tRNA modifying enzyme. (423 aa) | ||||
hemN2 | Possible oxygen-independent coproporphyrinogen III oxidase (hemN); Probably acts as a heme chaperone, transferring heme to an unknown acceptor. Binds one molecule of heme per monomer, possibly covalently. Binds 1 [4Fe-4S] cluster. The cluster is coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine. Belongs to the anaerobic coproporphyrinogen-III oxidase family. (385 aa) | ||||
nth | Endonuclease III DNA-(apurinic or apyrimidinic site) lyase; 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. (261 aa) | ||||
RPA0380 | Possible oxidoreductase similar to formate dehydrogenase and cbbBc of R. eutropha; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the prokaryotic molybdopterin-containing oxidoreductase family. (770 aa) | ||||
rlmN | Cfr family protein; Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs. m2A2503 modification seems to play a crucial role in the proofreading step occurring at the peptidyl transferase center and thus would serve to optimize ribosomal fidelity; Belongs to the radical SAM superfamily. RlmN family. (424 aa) | ||||
miaB | tRNA-i(6)A37 modification enzyme MiaB; Catalyzes the methylthiolation of N6-(dimethylallyl)adenosine (i(6)A), leading to the formation of 2-methylthio-N6- (dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine. (463 aa) | ||||
RPA0453 | Possible NifU-like domain (residues 119-187); Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (188 aa) | ||||
RPA0489 | Ferredoxin II; Ferredoxins are iron-sulfur proteins that transfer electrons in a wide variety of metabolic reactions. (112 aa) | ||||
gcpE | 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase (flavodoxin); Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME- 2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate. Belongs to the IspG family. (441 aa) | ||||
badF | benzoyl-CoA reductase subunit. (437 aa) | ||||
badG | benzoyl-CoA reductase subunit. (277 aa) | ||||
hbaB | 4-hydroxybenzoyl-CoA reductase, first of three subunits. (163 aa) | ||||
hbaD | 4-hydroxybenzoyl-CoA reductase, third of three subunits; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (327 aa) | ||||
gltA | Possible pyridine nucleotide-linked oxidoreductase, possible glutamate synthase; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (1035 aa) | ||||
RPA0679 | Protein of unknown function UPF0004:Elongator protein 3/MiaB/NifB. (677 aa) | ||||
phnJ | PhnJ protein, phosphonate metabolism, function unknown; Catalyzes the breakage of the C-P bond in alpha-D-ribose 1- methylphosphonate 5-phosphate (PRPn) forming alpha-D-ribose. Belongs to the PhnJ family. (292 aa) | ||||
fdsG | Putative NAD-dependent formate dehydrogenase gamma subunit. (156 aa) | ||||
fdsB | NAD-dependent formate dehydrogenase beta subunit. (518 aa) | ||||
fdsA | NAD-dependent formate dehydrogenase alpha subunit. (948 aa) | ||||
cysH | Putative phosphoadenosine phosphosulfate reductase; Reduction of activated sulfate into sulfite. (246 aa) | ||||
gltB | Glutamate synthase, large subunit; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (1575 aa) | ||||
gltD | Glutamate synthase (NADPH) small chain; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (484 aa) | ||||
RPA0933 | Putative protease, putative; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (325 aa) | ||||
RPA0934 | Conserved unknown protein; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (306 aa) | ||||
RPA0948 | Possible hypothetical RNA methyltransferase; Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family. (412 aa) | ||||
hupU | Uptake hydrogenase accessory protein hupU. (333 aa) | ||||
hupS | Uptake hydrogenase regulatory protein hupV pseudogene, frameshifted; Authentic frameshift, hupV pseudogene. (370 aa) | ||||
hypD | Hydrogenase expression/formation protein hypD; Belongs to the HypD family. (380 aa) | ||||
RPA0983 | Possible phthalate dioxygenase; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (452 aa) | ||||
fixG | Nitrogen fixation protein fixG, homologous to rdxB of R. sphaeroides; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (480 aa) | ||||
petA | Ubiquinol-cytochrome-c reductase, Rieske iron-sulfur protein; Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis. (177 aa) | ||||
RPA1017 | Nitrogen fixation-related protein. (130 aa) | ||||
RPA1033 | DUF85:Elongator protein 3/MiaB/NifB. (386 aa) | ||||
polN | Possible phage DNA polymerases. (276 aa) | ||||
RPA1037 | Possible electron transfer flavoprotein dehydrogenases; Accepts electrons from ETF and reduces ubiquinone. (552 aa) | ||||
nadA | Quinolinate synthetase A; Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate. (370 aa) | ||||
glcF | Glycolate oxidase subunit, (Fe-S)protein, GlcF. (437 aa) | ||||
queE | 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. (210 aa) | ||||
RPA1192 | Cytochrome b6-F complex iron-sulfur subunit; Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis. (208 aa) | ||||
iorA | Putative indolepyruvate ferredoxin oxidoreductase, alpha subunit; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (608 aa) | ||||
RPA1244 | Conserved unknown protein. (201 aa) | ||||
vnfX | Putative vanadium nitrogenase protein. (161 aa) | ||||
vnfH | Nitrogenase iron protein, vnfH; The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components: the iron protein and the molybdenum-iron protein; Belongs to the NifH/BchL/ChlL family. (296 aa) | ||||
vnfD | Nitrogenase vanadium-iron protein alpha chain. (472 aa) | ||||
vnfK | Nitrogenase vanadium-iron protein, VnfK subunit; Belongs to the NifD/NifK/NifE/NifN family. (462 aa) | ||||
RPA1382 | Nitrogen fixation-related protein. (161 aa) | ||||
anfK | Alternative nitrogenase 3 beta chain; Belongs to the NifD/NifK/NifE/NifN family. (461 aa) | ||||
anfD | Putative nitrogenase molybdenum-iron protein alpha chain (nitrogenase component I) (dinitrogenase). (522 aa) | ||||
anfH | Nitrogenase iron protein (nitrogenase component II) (nitrogenase reductase); The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components: the iron protein and the molybdenum-iron protein; Belongs to the NifH/BchL/ChlL family. (275 aa) | ||||
ilvD2 | Dihydroxy-acid dehydratase; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the IlvD/Edd family. (618 aa) | ||||
RPA1501 | Possible coenzyme F420 hydrogenase beta subunit. (409 aa) | ||||
bchX | Bacteriochlorophyllide reductase subunit BchX; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the NifH/BchL/ChlL family. (332 aa) | ||||
bchN | Protochlorophyllide reductase subunit BchN; Component of the dark-operative protochlorophyllide reductase (DPOR) that uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent. The NB-protein (BchN-BchB) is the catalytic component of the complex. (429 aa) | ||||
bchB | Protochlorophyllide reductase BchB subunit; Component of the dark-operative protochlorophyllide reductase (DPOR) that uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent. The NB-protein (BchN-BchB) is the catalytic component of the complex. (540 aa) | ||||
bchL | Protochlorophyllide reductase iron-sulfur ATP-binding protein BchL; Component of the dark-operative protochlorophyllide reductase (DPOR) that uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent. The L component serves as a unique electron donor to the NB-component of the complex, and binds Mg-ATP. (312 aa) | ||||
RPA1606 | Conserved unknown protein; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the glutaredoxin family. Monothiol subfamily. (127 aa) | ||||
hemN1 | Putative coproporphyrinogen oxidase III; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the anaerobic coproporphyrinogen-III oxidase family. (449 aa) | ||||
bchE | Mg-protoporphyrin IX monomethyl ester oxidative cyclase 66kD subunit; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (565 aa) | ||||
RPA1719 | Protein of unknown function UPF0153. (110 aa) | ||||
fdxA | Putative ferredoxin; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (75 aa) | ||||
ung | Uracil-DNA glycosylase:Phage SPO1 DNA polymerase-related protein. (495 aa) | ||||
RPA1800 | Elongator protein 3/MiaB/NifB. (416 aa) | ||||
thcC | Rhodocoxin; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (106 aa) | ||||
pqqE | Putative pyrroloquinoline quinone biosynthesis protein E; Catalyzes the cross-linking of a glutamate residue and a tyrosine residue in the PqqA protein as part of the biosynthesis of pyrroloquinoline quinone (PQQ). (377 aa) | ||||
RPA1974 | MRP protein(ATP/GTP-binding protein) homolog; Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP; Belongs to the Mrp/NBP35 ATP-binding proteins family. (370 aa) | ||||
moaA | Molybdenum biosynthetic protein A; Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate. (344 aa) | ||||
RPA2016 | Possible methyltransferase related protein. (652 aa) | ||||
bioB | Biotin synthetase; Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical-based mechanism; Belongs to the radical SAM superfamily. Biotin synthase family. (336 aa) | ||||
RPA2092 | Conserved hypothetical protein; InterPro IPR001450. (378 aa) | ||||
RPA2122 | Putative oxygen independent coproporphyrinogen III oxidase. (486 aa) | ||||
ilvD3 | Dihydroxy-acid dehydratase; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the IlvD/Edd family. (568 aa) | ||||
ilvD | Putative dihydroxy-acid dehydratase; Belongs to the IlvD/Edd family. (559 aa) | ||||
nifH1 | Putative nitrogenase NifH subunit; The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components: the iron protein and the molybdenum-iron protein; Belongs to the NifH/BchL/ChlL family. (291 aa) | ||||
nifB2 | Putative nitrogenase iron-molybdenum cofactor biosynthesis protein NifB. (307 aa) | ||||
RPA2355 | Possible nitrogenase NifB. (127 aa) | ||||
queH | DUF208; Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr). (199 aa) | ||||
nifS1 | Putative cysteine desulfurase, nifS homolog. (390 aa) | ||||
sufB | sufB, needed for fhuF Fe-S center stability. (493 aa) | ||||
RPA2468 | DUF59. (122 aa) | ||||
RPA2470 | Protein of unknown function, HesB/YadR/YfhF; Belongs to the HesB/IscA family. (123 aa) | ||||
RPA2493 | Possible P-methylase. (598 aa) | ||||
kamA | Putative L-lysine 2,3-aminomutase; Citation: Ruzicka et al. (2000) J. Bact. 182:469-476. (363 aa) | ||||
lipA2 | Lipoic acid synthetase; 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. (319 aa) | ||||
RPA2614 | Conserved hypothetical protein. (425 aa) | ||||
nifH2 | Putative nitrogenase iron protein (nitrogenase component II) (nitrogenase reductase); Belongs to the NifH/BchL/ChlL family. (290 aa) | ||||
nifB1 | Putative nitrogenase iron-molybdenum cofactor biosynthesis protein NifB. (298 aa) | ||||
nifH3 | Putative nitrogenase reductase NifH subunit; The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components: the iron protein and the molybdenum-iron protein; Belongs to the NifH/BchL/ChlL family. (289 aa) | ||||
rimO | Protein of unknown function UPF0004:Elongator protein 3/MiaB/NifB; Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12; Belongs to the methylthiotransferase family. RimO subfamily. (441 aa) | ||||
RPA2690 | Possible uracil-DNA glycosylase. (224 aa) | ||||
RPA2856 | Protein of unknown function, HesB/YadR/YfhF; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the HesB/IscA family. (110 aa) | ||||
nuoI1 | NADH-ubiquinone dehydrogenase chain I; NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. (162 aa) | ||||
nuoG1 | NADH-ubiquinone dehydrogenase chain G; NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. Belongs to the complex I 75 kDa subunit family. (694 aa) | ||||
nuoF1 | NADH-ubiquinone dehydrogenase chain F; NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. Belongs to the complex I 51 kDa subunit family. (441 aa) | ||||
nuoE1 | NADH-ubiquinone dehydrogenase chain E; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (249 aa) | ||||
nuoB1 | NADH-ubiquinone dehydrogenase chain B; NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. (198 aa) | ||||
RPA3088 | Conserved hypothetical protein; COGs COG0327. (130 aa) | ||||
RPA3195 | Related to Pyruvate ferredoxin/flavodoxin oxidoreductase; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (1161 aa) | ||||
RPA3324 | Hypothetical protein; InterPro IPR000183. (289 aa) | ||||
RPA3392 | Possible nifU homolog. (150 aa) | ||||
ilvD1 | Dihydroxy-acid dehydratase; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the IlvD/Edd family. (602 aa) | ||||
RPA3550 | Coenzyme B12-binding:Elongator protein 3/MiaB/NifB. (589 aa) | ||||
thiC | Thiamin biosynthesis protein thiC; 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. (666 aa) | ||||
vanA | Putative vanillate O-demethylase oxygenase, iron-sulfur subunit. (347 aa) | ||||
vanB | Putative vanillate O-demethylase oxidoreductase. (330 aa) | ||||
nirA | Possible ferredoxin-nitrite reductase; Belongs to the nitrite and sulfite reductase 4Fe-4S domain family. (590 aa) | ||||
RPA3711 | Possible sulfite reductase (NADPH). (539 aa) | ||||
lytB1 | Penicillin tolerance protein; Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP/MEP pathway for isoprenoid precursor biosynthesis. Belongs to the IspH family. (306 aa) | ||||
RPA3735 | Conserved unknown protein; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (386 aa) | ||||
RPA3748 | Elongator protein 3/MiaB/NifB. (527 aa) | ||||
RPA3764 | Putative 2Fe:2S ferredoxin; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (362 aa) | ||||
paaD | Putative phenylacetic acid degradation protein PaaD. (167 aa) | ||||
RPA3803 | Carbon-monoxide dehydrogenase small subunit; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (161 aa) | ||||
fumA | Fumarate hydratase, class I; Catalyzes the reversible hydration of fumarate to (S)-malate. Belongs to the class-I fumarase family. (551 aa) | ||||
RPA3956 | Ferredoxin; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (106 aa) | ||||
RPA3999 | Possible coenzyme PQQ synthesis protein E. (347 aa) | ||||
RPA4213 | Sulfite reductase hemoprotein subunit; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (551 aa) | ||||
RPA4231 | Putative oxidoreductase; Belongs to the prokaryotic molybdopterin-containing oxidoreductase family. (703 aa) | ||||
nuoI2 | NADH-ubiquinone dehydrogenase chain I; NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. (173 aa) | ||||
nuoG2 | NADH-ubiquinone dehydrogenase chain G; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (877 aa) | ||||
nuoF2 | NADH-ubiquinone dehydrogenase chain F. (428 aa) | ||||
nuoE2 | NADH-ubiquinone dehydrogenase chain E. (162 aa) | ||||
nuoB2 | NADH-ubiquinone dehydrogenase chain B; NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. (208 aa) | ||||
lytB2 | Penicillin tolerance protein (lytB), control of stringent response; Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP/MEP pathway for isoprenoid precursor biosynthesis. Belongs to the IspH family. (320 aa) | ||||
mutY | Adenine glycosylase mutY; Adenine glycosylase active on G-A mispairs. (349 aa) | ||||
RPA4493 | Conserved unknown protein. (221 aa) | ||||
RPA4507 | Elongator protein 3/MiaB/NifB. (594 aa) | ||||
fixX | Ferredoxin like protein, fixX; Could be a 3Fe-4S cluster-containing protein. (98 aa) | ||||
nifS2 | Nitrogenase cofactor synthesis protein nifS; Catalyzes the removal of elemental sulfur atoms from cysteine to produce alanine. (410 aa) | ||||
nifU | Putative nifU protein; May be involved in the formation or repair of [Fe-S] clusters present in iron-sulfur proteins. (328 aa) | ||||
RPA4610 | Protein of unknown function, HesB/YadR/YfhF; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished; Belongs to the HesB/IscA family. (106 aa) | ||||
fdxB | Ferredoxin 2[4Fe-4S] III, fdxB; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (103 aa) | ||||
nifX | Nitrogenase molybdenum-iron protein nifX; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (132 aa) | ||||
nifD | Nitrogenase molybdenum-iron protein alpha chain, nifD; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (487 aa) | ||||
nifH4 | Nitrogenase iron protein, nifH; The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components: the iron protein and the molybdenum-iron protein; Belongs to the NifH/BchL/ChlL family. (298 aa) | ||||
hesB | Protein of unknown function, HesB/YadR/YfhF; Belongs to the HesB/IscA family. (118 aa) | ||||
ferN | Ferredoxin 2[4Fe-4S], fdxN. (73 aa) | ||||
nifB | Nitrogen fixation protein nifB; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (518 aa) | ||||
fer1 | Ferredoxin 2[4Fe-4S], fdxN; Ferredoxins are iron-sulfur proteins that transfer electrons in a wide variety of metabolic reactions. (64 aa) | ||||
bisC | Biotin sulfoxide reductase; Belongs to the prokaryotic molybdopterin-containing oxidoreductase family. (769 aa) | ||||
coxS, | Carbon-monoxide dehydrogenase small subunit; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (156 aa) | ||||
RPA4721 | possible+E2677 pyruvate-flavodoxin oxidoreductase; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (1737 aa) | ||||
RPA4722 | Possible glutamate synthase, small subunit; Observed by proteomics; Citation: Proteomics from VerBerkmoes et al. (2003) unpublished. (944 aa) |