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Results 1 - 10 of 10
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EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 1.14.15.39(+)-epi-isozizaene + 2 reduced [2Fe-2S] ferredoxin + 2 H+ + O2 - Streptomyces coelicolor (5R,S)-albaflavenol + 2 oxidized [2Fe-2S] ferredoxin + H2O - ?
Display the reaction diagram Show all sequences 1.14.15.39(+)-epi-isozizaene + 2 reduced [2Fe-2S] ferredoxin + 2 H+ + O2 - Streptomyces coelicolor A3(2) (5R,S)-albaflavenol + 2 oxidized [2Fe-2S] ferredoxin + H2O - ?
Display the reaction diagram Show all sequences 1.14.15.39(+)-epi-isozizaene + 4 reduced [2Fe-2S] ferredoxin + 4 H+ + 2 O2 - Streptomyces coelicolor albaflavenone + 4 oxidized [2Fe-2S] ferredoxin + 3 H2O - ?
Display the reaction diagram Show all sequences 1.14.15.39(+)-epi-isozizaene + 4 reduced [2Fe-2S] ferredoxin + 4 H+ + 2 O2 - Streptomyces coelicolor A3(2) M145 albaflavenone + 4 oxidized [2Fe-2S] ferredoxin + 3 H2O - ?
Display the reaction diagram Show all sequences 1.14.15.39(5R,S)-albaflavenol + 2 reduced [2Fe-2S] ferredoxin + 2 H+ + O2 - Streptomyces coelicolor albaflavenone + 2 oxidized [2Fe-2S] ferredoxin + 2 H2O - ?
Display the reaction diagram Show all sequences 1.14.15.39(5R,S)-albaflavenol + 2 reduced [2Fe-2S] ferredoxin + 2 H+ + O2 - Streptomyces coelicolor A3(2) albaflavenone + 2 oxidized [2Fe-2S] ferredoxin + 2 H2O - ?
Display the reaction diagram Show all sequences 1.14.15.39more enzyme catalyses two sequential allylic oxidation reactions. The substrate epi-isozizaene is first oxidized to yield the epimeric intermediates (5R)-albaflavenol and (5S)-albaflavenol, which can be further oxidized to yield the sesquiterpenoid antibiotic albaflavenone. Proposed mechanism of biosynthesis of albaflavenone catalyzed by CYP170A1 Streptomyces coelicolor ? - ?
Display the reaction diagram Show all sequences 1.14.15.39more the bifunctional enzyme is able to also generate farnesene isomers from farnesyl diphosphate: (E)-beta-farnesene (61%), (3E,6E)-alpha-farnesene (26%), (3Z,6E)-alpha-farnesene (6.8%), nerolidol (4.9%), and farnesol(1.8%) Streptomyces coelicolor ? - ?
Display the reaction diagram Show all sequences 1.14.15.39more enzyme catalyses two sequential allylic oxidation reactions. The substrate epi-isozizaene is first oxidized to yield the epimeric intermediates (5R)-albaflavenol and (5S)-albaflavenol, which can be further oxidized to yield the sesquiterpenoid antibiotic albaflavenone. Proposed mechanism of biosynthesis of albaflavenone catalyzed by CYP170A1 Streptomyces coelicolor A3(2) ? - ?
Display the reaction diagram Show all sequences 1.14.15.39more the bifunctional enzyme is able to also generate farnesene isomers from farnesyl diphosphate: (E)-beta-farnesene (61%), (3E,6E)-alpha-farnesene (26%), (3Z,6E)-alpha-farnesene (6.8%), nerolidol (4.9%), and farnesol(1.8%) Streptomyces coelicolor A3(2) M145 ? - ?
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