STRINGSTRING
acnA acnA pufB pufB pufA pufA pufL pufL pufM pufM pufC pufC BVIR_702 BVIR_702 BVIR_704 BVIR_704 aceB aceB cycA cycA lutA lutA BVIR_1017 BVIR_1017 glgB glgB hyfB hyfB glgC glgC hycD hycD hyfE hyfE nuoM_1 nuoM_1 hycE hycE hycG hycG glgA1 glgA1 ndhC ndhC nuoB nuoB nqo5 nqo5 nuoD nuoD nqo2 nqo2 nqo1 nqo1 nqo3 nqo3 nuoH nuoH nuoI nuoI nuoJ nuoJ nuoK nuoK nuoL nuoL nuoM_2 nuoM_2 nrfB nrfB rpiA_1 rpiA_1 ccpA ccpA tal tal BVIR_965 BVIR_965 nuoN nuoN petA_1 petA_1 BVIR_1475 BVIR_1475 yodB yodB tpiA tpiA BVIR_1612 BVIR_1612 BVIR_1692 BVIR_1692 pntA pntA pntB pntB ifcA ifcA etfA_2 etfA_2 adhC2 adhC2 etfB_2 etfB_2 BVIR_1818 BVIR_1818 ratA ratA pdhC pdhC eno eno BVIR_1961 BVIR_1961 cobC cobC BVIR_2028 BVIR_2028 fccA fccA hgdC_1 hgdC_1 hgdC_2 hgdC_2 hgdC_3 hgdC_3 prpC prpC isiB isiB etfB_1 etfB_1 etfA_1 etfA_1 BVIR_2266 BVIR_2266 fer1 fer1 porB porB adh adh pgk pgk BVIR_2397 BVIR_2397 aarA aarA yceJ yceJ shp shp BVIR_2471 BVIR_2471 petC petC petB petB petA petA glgX_1 glgX_1 BVIR_2536 BVIR_2536 hybE hybE hupC hupC hoxL hoxL hoxK hoxK cydA cydA cydB cydB sucB sucB sucA sucA sucD_1 sucD_1 sucC sucC mdh mdh sdhB sdhB sdhA sdhA BVIR_2657 BVIR_2657 sdhC sdhC pgi_1 pgi_1 hgdC_4 hgdC_4 kamA_1 kamA_1 glk glk fixP fixP BVIR_2881 BVIR_2881 BVIR_2882 BVIR_2882 fumC fumC gpmA gpmA frdA frdA frdB frdB frdC frdC kamA_2 kamA_2 pyk pyk BVIR_3179 BVIR_3179 ubiE_5 ubiE_5 BVIR_3212 BVIR_3212 fdxA fdxA BVIR_454 BVIR_454 BVIR_455 BVIR_455 BVIR_458 BVIR_458 cycB cycB BVIR_498 BVIR_498 ubiE_1 ubiE_1 BVIR_568 BVIR_568 puhA puhA rpe_1 rpe_1 tktA tktA
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splice isoforms or post-translational modifications are collapsed, i.e. each node represents all the proteins produced by a single, protein-coding gene locus.
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colored nodes:
query proteins and first shell of interactors
white nodes:
second shell of interactors
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empty nodes:
proteins of unknown 3D structure
filled nodes:
a 3D structure is known or predicted
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Edges represent protein-protein associations
associations are meant to be specific and meaningful, i.e. proteins jointly contribute to a shared function; this does not necessarily mean they are physically binding to each other.
Known Interactions
from curated databases
experimentally determined
Predicted Interactions
gene neighborhood
gene fusions
gene co-occurrence
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textmining
co-expression
protein homology
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acnAAconitate hydratase 1; Catalyzes the isomerization of citrate to isocitrate via cis- aconitate. (902 aa)
pufBLight-harvesting protein B-1015 beta chain precursor; Antenna complexes are light-harvesting systems, which transfer the excitation energy to the reaction centers. (69 aa)
pufALight-harvesting protein B-1015 alpha chain precursor; Antenna complexes are light-harvesting systems, which transfer the excitation energy to the reaction centers. (69 aa)
pufLReaction center protein L chain; The reaction center is a membrane-bound complex that mediates the initial photochemical event in the electron transfer process of photosynthesis. (274 aa)
pufMReaction center protein M chain; The reaction center is a membrane-bound complex that mediates the initial photochemical event in the electron transfer process of photosynthesis. (324 aa)
pufCPhotosynthetic reaction center cytochrome c subunit precursor; The reaction center of purple bacteria contains a tightly bound cytochrome molecule which re-reduces the photo oxidized primary electron donor. (356 aa)
BVIR_702Electron transfer flavoprotein-ubiquinone oxidoreductase; Accepts electrons from ETF and reduces ubiquinone. (555 aa)
BVIR_704Indolepyruvate ferredoxin oxidoreductase. (1164 aa)
aceBMalate synthase A; Belongs to the malate synthase family. (999 aa)
cycACytochrome c2 precursor; Cytochrome c2 is found mainly in purple, non-sulfur, photosynthetic bacteria where it functions as the electron donor to the oxidized bacteriochlorophyll in the photophosphorylation pathway. However, it may also have a role in the respiratory chain and is found in some non-photosynthetic bacteria. (127 aa)
lutALactate utilization protein A. (260 aa)
BVIR_1017Isocitrate dehydrogenase [NADP]; Belongs to the isocitrate and isopropylmalate dehydrogenases family. (405 aa)
glgB1,4-alpha-glucan branching enzyme GlgB; Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position; Belongs to the glycosyl hydrolase 13 family. GlgB subfamily. (730 aa)
hyfBHydrogenase-4 component B. (672 aa)
glgCGlucose-1-phosphate adenylyltransferase; Involved in the biosynthesis of ADP-glucose, a building block required for the elongation reactions to produce glycogen. Catalyzes the reaction between ATP and alpha-D-glucose 1-phosphate (G1P) to produce pyrophosphate and ADP-Glc; Belongs to the bacterial/plant glucose-1-phosphate adenylyltransferase family. (439 aa)
hycDFormate hydrogenlyase subunit 4. (325 aa)
hyfEHydrogenase-4 component E. (223 aa)
nuoM_1NADH-quinone oxidoreductase subunit M. (482 aa)
hycEFormate hydrogenlyase subunit 5 precursor. (497 aa)
hycGFormate hydrogenlyase subunit 7. (174 aa)
glgA1Glycogen synthase 1; Synthesizes alpha-1,4-glucan chains using ADP-glucose. (548 aa)
ndhCNAD(P)H-quinone oxidoreductase subunit 3; 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; Belongs to the complex I subunit 3 family. (121 aa)
nuoBNADH-quinone oxidoreductase subunit 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. (192 aa)
nqo5NADH-quinone oxidoreductase subunit C 1; 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; Belongs to the complex I 30 kDa subunit family. (212 aa)
nuoDNADH-quinone oxidoreductase subunit D; 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; Belongs to the complex I 49 kDa subunit family. (397 aa)
nqo2NADH-quinone oxidoreductase chain 2. (258 aa)
nqo1NADH-quinone oxidoreductase chain 1; 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. (435 aa)
nqo3NADH-quinone oxidoreductase chain 3; 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. (692 aa)
nuoHNADH-quinone oxidoreductase subunit H; 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. This subunit may bind ubiquinone. (348 aa)
nuoINADH-quinone oxidoreductase subunit 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)
nuoJNADH-quinone oxidoreductase subunit J; 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. (203 aa)
nuoKNADH-quinone oxidoreductase subunit K; 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; Belongs to the complex I subunit 4L family. (102 aa)
nuoLNADH-quinone oxidoreductase subunit L. (659 aa)
nuoM_2NADH-quinone oxidoreductase subunit M. (503 aa)
nrfBCytochrome c-type protein NrfB precursor. (431 aa)
rpiA_1Ribose-5-phosphate isomerase A; Catalyzes the reversible conversion of ribose-5-phosphate to ribulose 5-phosphate. (238 aa)
ccpACytochrome c551 peroxidase precursor. (344 aa)
talTransaldolase. (257 aa)
BVIR_965Ferredoxin-6. (106 aa)
nuoNNADH-quinone oxidoreductase subunit N; 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; Belongs to the complex I subunit 2 family. (484 aa)
petA_1Ubiquinol-cytochrome c reductase 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. (183 aa)
BVIR_1475Hypothetical protein. (194 aa)
yodBHypothetical protein. (205 aa)
tpiATriosephosphate 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. (266 aa)
BVIR_1612Hypothetical protein. (224 aa)
BVIR_1692Hypothetical protein. (100 aa)
pntANAD(P) transhydrogenase subunit alpha. (143 aa)
pntBNAD(P) transhydrogenase subunit beta; The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane; Belongs to the PNT beta subunit family. (466 aa)
ifcAFumarate reductase flavoprotein subunit precursor. (445 aa)
etfA_2Electron transfer flavoprotein subunit alpha. (315 aa)
adhC2NADP-dependent alcohol dehydrogenase C 2. (353 aa)
etfB_2Electron transfer flavoprotein subunit beta. (249 aa)
BVIR_1818Rubredoxin. (100 aa)
ratARibosome association toxin RatA. (157 aa)
pdhCDihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex; The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). (452 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. (427 aa)
BVIR_1961Glucosyl-3-phosphoglycerate phosphatase. (209 aa)
cobCPutative phosphoserine phosphatase 2. (180 aa)
BVIR_2028Hydrogen cyanide synthase subunit HcnA. (98 aa)
fccACytochrome subunit of sulfide dehydrogenase. (111 aa)
hgdC_1R-phenyllactate dehydratase activator. (282 aa)
hgdC_2R-phenyllactate dehydratase activator. (669 aa)
hgdC_3Activator of (R)-2-hydroxyglutaryl-CoA dehydratase. (350 aa)
prpC2-methylcitrate synthase; Belongs to the citrate synthase family. (403 aa)
isiBFlavodoxin; Low-potential electron donor to a number of redox enzymes. Belongs to the flavodoxin family. (160 aa)
etfB_1Acryloyl-CoA reductase electron transfer subunit gamma. (281 aa)
etfA_1Acryloyl-CoA reductase electron transfer subunit beta. (368 aa)
BVIR_22662Fe-2S iron-sulfur cluster binding domain protein. (121 aa)
fer1Ferredoxin-1. (63 aa)
porBPyruvate-flavodoxin oxidoreductase. (1659 aa)
adhAlcohol dehydrogenase. (336 aa)
pgkPhosphoglycerate kinase; Belongs to the phosphoglycerate kinase family. (397 aa)
BVIR_2397Hypothetical protein. (120 aa)
aarACitrate synthase; Belongs to the citrate synthase family. (440 aa)
yceJHypothetical protein. (184 aa)
shpCytochrome c-type protein SHP precursor. (144 aa)
BVIR_2471Dihem cytochrome c. (177 aa)
petCCytochrome b/c1; 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. c1 functions as an electron donor to cytochrome c. (282 aa)
petBCytochrome b/c1; 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. (419 aa)
petAUbiquinol-cytochrome c reductase 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; Belongs to the Rieske iron-sulfur protein family. (179 aa)
glgX_1Glycogen debranching enzyme; Belongs to the glycosyl hydrolase 13 family. (738 aa)
BVIR_2536Nickel-dependent hydrogenase. (351 aa)
hybEHydrogenase-2 operon protein HybE. (169 aa)
hupCPutative Ni/Fe-hydrogenase B-type cytochrome subunit. (262 aa)
hoxLUptake hydrogenase large subunit; Belongs to the [NiFe]/[NiFeSe] hydrogenase large subunit family. (596 aa)
hoxKUptake hydrogenase small subunit precursor. (375 aa)
cydACytochrome bd-I ubiquinol oxidase subunit 1. (469 aa)
cydBCytochrome bd-I ubiquinol oxidase subunit 2. (334 aa)
sucBDihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex; E2 component of the 2-oxoglutarate dehydrogenase (OGDH) complex which catalyzes the second step in the conversion of 2- oxoglutarate to succinyl-CoA and CO(2). (410 aa)
sucA2-oxoglutarate dehydrogenase E1 component. (988 aa)
sucD_1Succinyl-CoA ligase [ADP-forming] subunit alpha; Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit. (294 aa)
sucCSuccinyl-CoA ligase [ADP-forming] subunit beta; Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit. (399 aa)
mdhMalate dehydrogenase; Catalyzes the reversible oxidation of malate to oxaloacetate. Belongs to the LDH/MDH superfamily. MDH type 3 family. (321 aa)
sdhBSuccinate dehydrogenase iron-sulfur subunit; Belongs to the succinate dehydrogenase/fumarate reductase iron-sulfur protein family. (259 aa)
sdhASuccinate dehydrogenase flavoprotein subunit; Belongs to the FAD-dependent oxidoreductase 2 family. FRD/SDH subfamily. (609 aa)
BVIR_2657Succinate dehydrogenase/Fumarate reductase transmembrane subunit. (131 aa)
sdhCSuccinate dehydrogenase cytochrome b556 subunit. (132 aa)
pgi_1Glucose-6-phosphate isomerase. (439 aa)
hgdC_4R-phenyllactate dehydratase activator. (256 aa)
kamA_1L-lysine 2,3-aminomutase. (476 aa)
glkGlucokinase; Belongs to the bacterial glucokinase family. (324 aa)
fixPCbb3-type cytochrome c oxidase subunit FixP; C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex. (298 aa)
BVIR_2881Cytochrome C oxidase, mono-heme subunit/FixO. (245 aa)
BVIR_2882Hypothetical protein; Belongs to the heme-copper respiratory oxidase family. (550 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. (466 aa)
gpmA2,3-bisphosphoglycerate-dependent phosphoglycerate mutase; Catalyzes the interconversion of 2-phosphoglycerate and 3- phosphoglycerate; Belongs to the phosphoglycerate mutase family. BPG- dependent PGAM subfamily. (207 aa)
frdAFumarate reductase flavoprotein subunit. (588 aa)
frdBFumarate reductase iron-sulfur subunit; Belongs to the succinate dehydrogenase/fumarate reductase iron-sulfur protein family. (250 aa)
frdCFumarate reductase subunit C. (150 aa)
kamA_2L-lysine 2,3-aminomutase. (356 aa)
pykPyruvate kinase; Belongs to the pyruvate kinase family. (477 aa)
BVIR_3179Hypothetical protein. (372 aa)
ubiE_5Ubiquinone/menaquinone biosynthesis C-methyltransferase UbiE; Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3- methyl-6-methoxy-1,4-benzoquinol (DMQH2). (257 aa)
BVIR_3212Hypothetical protein. (262 aa)
fdxAFerredoxin-2; Ferredoxins are iron-sulfur proteins that transfer electrons in a wide variety of metabolic reactions. (111 aa)
BVIR_4542-oxoglutarate ferredoxin oxidoreductase subunit gamma. (184 aa)
BVIR_4552-oxoglutarate oxidoreductase subunit KorB. (281 aa)
BVIR_458NAD(P)H-quinone oxidoreductase subunit I, chloroplastic; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (604 aa)
cycBCytochrome c-552 precursor. (104 aa)
BVIR_498NADP-reducing hydrogenase subunit HndC. (642 aa)
ubiE_1Ubiquinone/menaquinone biosynthesis C-methyltransferase UbiE; Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3- methyl-6-methoxy-1,4-benzoquinol (DMQH2). (241 aa)
BVIR_568B12 binding domain protein. (341 aa)
puhAReaction center protein H chain; The reaction center is a membrane-bound complex that mediates the initial photochemical event in the electron transfer process of photosynthesis. (258 aa)
rpe_1Ribulose-phosphate 3-epimerase; Belongs to the ribulose-phosphate 3-epimerase family. (225 aa)
tktATransketolase 1; Belongs to the transketolase family. (672 aa)
Your Current Organism:
Blastochloris viridis
NCBI taxonomy Id: 1079
Other names: ATCC 19567, B. viridis, CCUG 30818, CCUG 7830, DSM 133, LMG 4321, LMG:4321, NBRC 102659, Rhodopseudomonas viridis, strain G. Drews F
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