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Results 1 - 8 of 8
EC Number Reaction Commentary Reference
Show all pathways known for 1.3.7.8Display the word mapDisplay the reaction diagram Show all sequences 1.3.7.8cyclohexa-1,5-diene-1-carbonyl-CoA + oxidized ferredoxin + 2 ADP + 2 phosphate = benzoyl-CoA + reduced ferredoxin + 2 ATP + 2 H2O - -
Show all pathways known for 1.3.7.8Display the word mapDisplay the reaction diagram Show all sequences 1.3.7.8cyclohexa-1,5-diene-1-carbonyl-CoA + oxidized ferredoxin + 2 ADP + 2 phosphate = benzoyl-CoA + reduced ferredoxin + 2 ATP + 2 H2O ATP-binding switch is rather fast, reverse switch back of MgADP-bound enzyme is considered rate-limiting, binding of nucleotides does not affect redox potential of 4Fe-4S clusters 654733
Show all pathways known for 1.3.7.8Display the word mapDisplay the reaction diagram Show all sequences 1.3.7.8cyclohexa-1,5-diene-1-carbonyl-CoA + oxidized ferredoxin + 2 ADP + 2 phosphate = benzoyl-CoA + reduced ferredoxin + 2 ATP + 2 H2O ATP-hydrolysis-driven electron transfer with transient formation of a phosphorylated enzyme, ATPase- and autophosphatase-partial activities exhibit identical redox dependencies 657182
Show all pathways known for 1.3.7.8Display the word mapDisplay the reaction diagram Show all sequences 1.3.7.8cyclohexa-1,5-diene-1-carbonyl-CoA + oxidized ferredoxin + 2 ADP + 2 phosphate = benzoyl-CoA + reduced ferredoxin + 2 ATP + 2 H2O benzoyl-CoA reduction is initiated by a hydrogen atom transfer from a W(IV) species with an aqua ligand, yielding W(V)-[OH-] and a substrate radical intermediate. In the next step, a proton-assisted second electron transfer takes place with a conserved active-site histidine serving as the second proton donor. The electron for the second reduction step is taken from the pyranopterin cofactors rather than from the tungsten ion. The resulting cationic radical, which is distributed over both pyranopterins, is stabilized by conserved anionic amino acid residues, reaction mechanism, detailed overview -, 763184
Show all pathways known for 1.3.7.8Display the word mapDisplay the reaction diagram Show all sequences 1.3.7.8cyclohexa-1,5-diene-1-carbonyl-CoA + oxidized ferredoxin + 2 ADP + 2 phosphate = benzoyl-CoA + reduced ferredoxin + 2 ATP + 2 H2O Birch-like mechanism 654733
Show all pathways known for 1.3.7.8Display the word mapDisplay the reaction diagram Show all sequences 1.3.7.8cyclohexa-1,5-diene-1-carbonyl-CoA + oxidized ferredoxin + 2 ADP + 2 phosphate = benzoyl-CoA + reduced ferredoxin + 2 ATP + 2 H2O Birch-like reduction with base-catalyzed rearrangement to 1,5-diene 285200
Show all pathways known for 1.3.7.8Display the word mapDisplay the reaction diagram Show all sequences 1.3.7.8cyclohexa-1,5-diene-1-carbonyl-CoA + oxidized ferredoxin + 2 ADP + 2 phosphate = benzoyl-CoA + reduced ferredoxin + 2 ATP + 2 H2O class II BCRs drive BzCoA reduction by flavin-based electron bifurcation (FBEB) -, 762977
Show all pathways known for 1.3.7.8Display the word mapDisplay the reaction diagram Show all sequences 1.3.7.8cyclohexa-1,5-diene-1-carbonyl-CoA + oxidized ferredoxin + 2 ADP + 2 phosphate = benzoyl-CoA + reduced ferredoxin + 2 ATP + 2 H2O reaction mechanism, quantum mechanical/molecular mechanical (QM/MM) calculations 763132
Results 1 - 8 of 8