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ccoP | Unannotated protein; C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex. (311 aa) | ||||
ccoN | Unannotated protein; Belongs to the heme-copper respiratory oxidase family. (474 aa) | ||||
gltA | Unannotated protein; Belongs to the citrate synthase family. (429 aa) | ||||
RK21_00907 | Unannotated protein. (128 aa) | ||||
sdhD | Unannotated protein; Membrane-anchoring subunit of succinate dehydrogenase (SDH). (122 aa) | ||||
sdhB | Unannotated protein. (234 aa) | ||||
CMV24_07535 | Unannotated protein. (943 aa) | ||||
sucC | Unannotated protein; Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit. (388 aa) | ||||
sucD | Unannotated protein; 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) | ||||
ubiE | Unannotated protein; 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). (256 aa) | ||||
mdh | Unannotated protein; Catalyzes the reversible oxidation of malate to oxaloacetate. Belongs to the LDH/MDH superfamily. MDH type 3 family. (312 aa) | ||||
cyoD | Unannotated protein. (110 aa) | ||||
GCA_000688275_01625 | Unannotated protein. (252 aa) | ||||
RK21_01533 | Unannotated protein. (270 aa) | ||||
acnB | Unannotated protein; Belongs to the aconitase/IPM isomerase family. (697 aa) | ||||
RK21_03111 | Unannotated protein. (885 aa) | ||||
CMV24_15380 | Unannotated protein; Belongs to the citrate synthase family. (375 aa) | ||||
RK21_05190 | Unannotated protein; Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B). (375 aa) | ||||
ctaD | Unannotated protein; Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B. (529 aa) | ||||
CMV24_25300 | Unannotated protein. (295 aa) | ||||
glcB | Unannotated protein; Involved in the glycolate utilization. Catalyzes the condensation and subsequent hydrolysis of acetyl-coenzyme A (acetyl- CoA) and glyoxylate to form malate and CoA; Belongs to the malate synthase family. GlcB subfamily. (725 aa) | ||||
RK21_03318 | Unannotated protein; Catalyzes the isomerization of citrate to isocitrate via cis- aconitate. (913 aa) | ||||
RK21_04975 | Unannotated protein. (485 aa) | ||||
CMV24_20270 | Unannotated protein. (559 aa) | ||||
fumC | Unannotated protein; Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate; Belongs to the class-II fumarase/aspartase family. Fumarase subfamily. (464 aa) | ||||
RK21_03446 | Unannotated protein. (254 aa) | ||||
fumC-2 | Unannotated protein; Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate; Belongs to the class-II fumarase/aspartase family. Fumarase subfamily. (458 aa) | ||||
CMV24_15955 | Unannotated protein. (441 aa) | ||||
RK21_00978 | Unannotated protein; 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. (904 aa) | ||||
nuoH | Unannotated protein; 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. (335 aa) | ||||
nuoI | Unannotated protein; 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. (182 aa) | ||||
nuoK | Unannotated protein; 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) | ||||
CMV24_15885 | Unannotated protein. (617 aa) | ||||
CMV24_15880 | Unannotated protein. (510 aa) | ||||
nuoN | Unannotated protein; 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. (489 aa) | ||||
cydB | Unannotated protein. (335 aa) | ||||
RK21_00036 | Unannotated protein. (478 aa) | ||||
GCA_000688275_04669 | Unannotated protein. (614 aa) | ||||
GCA_000688275_04684 | Unannotated protein. (169 aa) | ||||
CMV24_16405 | Unannotated protein; Belongs to the monomeric-type IDH family. (741 aa) | ||||
CMV24_16410 | Unannotated protein. (418 aa) | ||||
RK21_04134 | Unannotated protein. (207 aa) | ||||
cyoB | Unannotated protein; Belongs to the heme-copper respiratory oxidase family. (672 aa) | ||||
RK21_04136 | Unannotated protein. (314 aa) | ||||
mqo-2 | Unannotated protein. (501 aa) | ||||
mqo | Unannotated protein. (545 aa) | ||||
ppc | Unannotated protein; Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle; Belongs to the PEPCase type 1 family. (875 aa) | ||||
aceK | Unannotated protein; Bifunctional enzyme which can phosphorylate or dephosphorylate isocitrate dehydrogenase (IDH) on a specific serine residue. This is a regulatory mechanism which enables bacteria to bypass the Krebs cycle via the glyoxylate shunt in response to the source of carbon. When bacteria are grown on glucose, IDH is fully active and unphosphorylated, but when grown on acetate or ethanol, the activity of IDH declines drastically concomitant with its phosphorylation. (569 aa) | ||||
ccoP-2 | Unannotated protein; C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex. (325 aa) | ||||
ccoN-2 | Unannotated protein; Belongs to the heme-copper respiratory oxidase family. (480 aa) |