EC Number | Cloned (Comment) | Organism |
---|---|---|
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Petunia x hybrida |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Vinca major |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Pericallis cruenta |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Delphinium grandiflorum |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Glycine max |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Gossypium hirsutum |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Nierembergia sp. |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Lycianthes rantonnei |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Solanum melongena |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Solanum tuberosum |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Torenia hybrid cultivar |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Glandularia x hybrida |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Callistephus chinensis |
1.14.14.81 | DNA and amino acid sequence determination and analysis, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Osteospermum hybrid cultivar |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Perilla frutescens |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Allium cepa |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Arabidopsis thaliana |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Gentiana triflora |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Glycine max |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Ipomoea nil |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Pelargonium x hortorum |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Petunia x hybrida |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Matthiola incana |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Torenia hybrid cultivar |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Callistephus chinensis |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Osteospermum hybrid cultivar |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Gerbera hybrid cultivar |
1.14.14.82 | DNA and amino acid sequence determination and analysis, detailed phylogenetic analysis and comparison of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, overview | Pilosella officinarum |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
1.14.14.81 | microsome | - |
Petunia x hybrida | - |
- |
1.14.14.81 | microsome | - |
Vinca major | - |
- |
1.14.14.81 | microsome | - |
Pericallis cruenta | - |
- |
1.14.14.81 | microsome | - |
Delphinium grandiflorum | - |
- |
1.14.14.81 | microsome | - |
Glycine max | - |
- |
1.14.14.81 | microsome | - |
Gossypium hirsutum | - |
- |
1.14.14.81 | microsome | - |
Nierembergia sp. | - |
- |
1.14.14.81 | microsome | - |
Lycianthes rantonnei | - |
- |
1.14.14.81 | microsome | - |
Solanum melongena | - |
- |
1.14.14.81 | microsome | - |
Solanum tuberosum | - |
- |
1.14.14.81 | microsome | - |
Torenia hybrid cultivar | - |
- |
1.14.14.81 | microsome | - |
Glandularia x hybrida | - |
- |
1.14.14.81 | microsome | - |
Callistephus chinensis | - |
- |
1.14.14.81 | microsome | - |
Osteospermum hybrid cultivar | - |
- |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.14.14.81 | additional information | Petunia x hybrida | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Vinca major | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Pericallis cruenta | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Delphinium grandiflorum | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Glycine max | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Gossypium hirsutum | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Nierembergia sp. | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Lycianthes rantonnei | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Solanum melongena | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Solanum tuberosum | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Torenia hybrid cultivar | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Glandularia x hybrida | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Callistephus chinensis | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.81 | additional information | Osteospermum hybrid cultivar | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Perilla frutescens | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Allium cepa | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Arabidopsis thaliana | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Gentiana triflora | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Glycine max | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Ipomoea nil | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Pelargonium x hortorum | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Petunia x hybrida | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Matthiola incana | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Torenia hybrid cultivar | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Callistephus chinensis | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Osteospermum hybrid cultivar | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Gerbera hybrid cultivar | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | Pilosella officinarum | - |
dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | additional information | Perilla frutescens | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Allium cepa | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Arabidopsis thaliana | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Gentiana triflora | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Glycine max | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Ipomoea nil | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Pelargonium x hortorum | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Petunia x hybrida | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Matthiola incana | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Torenia hybrid cultivar | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Callistephus chinensis | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Osteospermum hybrid cultivar | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Gerbera hybrid cultivar | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | additional information | Pilosella officinarum | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | ? | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Perilla frutescens | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Allium cepa | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Arabidopsis thaliana | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Gentiana triflora | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Glycine max | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Ipomoea nil | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Pelargonium x hortorum | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Petunia x hybrida | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Matthiola incana | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Torenia hybrid cultivar | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Callistephus chinensis | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Osteospermum hybrid cultivar | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Gerbera hybrid cultivar | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | Pilosella officinarum | - |
eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
1.14.14.81 | Callistephus chinensis | Q9FPN4 | line '01' | - |
1.14.14.81 | Delphinium grandiflorum | Q52YL8 | - |
- |
1.14.14.81 | Glandularia x hybrida | Q6J210 | - |
- |
1.14.14.81 | Glycine max | Q6YLS3 | - |
- |
1.14.14.81 | Gossypium hirsutum | Q84NG3 | i.e. Gossypium maxicanum | - |
1.14.14.81 | Lycianthes rantonnei | Q9FPN3 | blue potato bush | - |
1.14.14.81 | Nierembergia sp. | Q8LP20 | - |
- |
1.14.14.81 | Osteospermum hybrid cultivar | Q304Q4 | cv. Bamba | - |
1.14.14.81 | Pericallis cruenta | Q304Q5 | cv. Blue Bicolor | - |
1.14.14.81 | Petunia x hybrida | P48418 | - |
- |
1.14.14.81 | Solanum melongena | P37120 | - |
- |
1.14.14.81 | Solanum tuberosum | Q5EWY2 | - |
- |
1.14.14.81 | Torenia hybrid cultivar | Q9FS35 | hybrid cultivar | - |
1.14.14.81 | Vinca major | Q76LL4 | - |
- |
1.14.14.82 | Allium cepa | Q6QHJ9 | - |
- |
1.14.14.82 | Arabidopsis thaliana | Q9SD85 | - |
- |
1.14.14.82 | Callistephus chinensis | Q9FPN5 | line '01' | - |
1.14.14.82 | Gentiana triflora | Q59I68 | - |
- |
1.14.14.82 | Gerbera hybrid cultivar | Q38L00 | - |
- |
1.14.14.82 | Glycine max | Q8W3Y5 | - |
- |
1.14.14.82 | Ipomoea nil | Q767R1 | i.e. Pharbitis nil, cv. japanese morning glory | - |
1.14.14.82 | Matthiola incana | Q9FPN2 | - |
- |
1.14.14.82 | Osteospermum hybrid cultivar | Q304R0 | cv. Bamba | - |
1.14.14.82 | Pelargonium x hortorum | Q9FPM9 | - |
- |
1.14.14.82 | Perilla frutescens | Q93XJ2 | var. crispa | - |
1.14.14.82 | Petunia x hybrida | Q9SBQ9 | - |
- |
1.14.14.82 | Pilosella officinarum | Q0QLB3 | - |
- |
1.14.14.82 | Torenia hybrid cultivar | Q8S9C6 | gene ght | - |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
1.14.14.81 | flower | - |
Petunia x hybrida | - |
1.14.14.81 | flower | - |
Vinca major | - |
1.14.14.81 | flower | - |
Pericallis cruenta | - |
1.14.14.81 | flower | - |
Delphinium grandiflorum | - |
1.14.14.81 | flower | - |
Glycine max | - |
1.14.14.81 | flower | - |
Gossypium hirsutum | - |
1.14.14.81 | flower | - |
Nierembergia sp. | - |
1.14.14.81 | flower | - |
Lycianthes rantonnei | - |
1.14.14.81 | flower | - |
Solanum melongena | - |
1.14.14.81 | flower | - |
Solanum tuberosum | - |
1.14.14.81 | flower | - |
Torenia hybrid cultivar | - |
1.14.14.81 | flower | - |
Glandularia x hybrida | - |
1.14.14.81 | flower | - |
Callistephus chinensis | - |
1.14.14.81 | flower | - |
Osteospermum hybrid cultivar | - |
1.14.14.81 | petal | - |
Petunia x hybrida | - |
1.14.14.81 | petal | - |
Vinca major | - |
1.14.14.81 | petal | - |
Pericallis cruenta | - |
1.14.14.81 | petal | - |
Delphinium grandiflorum | - |
1.14.14.81 | petal | - |
Glycine max | - |
1.14.14.81 | petal | - |
Gossypium hirsutum | - |
1.14.14.81 | petal | - |
Nierembergia sp. | - |
1.14.14.81 | petal | - |
Lycianthes rantonnei | - |
1.14.14.81 | petal | - |
Solanum melongena | - |
1.14.14.81 | petal | - |
Solanum tuberosum | - |
1.14.14.81 | petal | - |
Torenia hybrid cultivar | - |
1.14.14.81 | petal | - |
Glandularia x hybrida | - |
1.14.14.81 | petal | - |
Callistephus chinensis | - |
1.14.14.81 | petal | - |
Osteospermum hybrid cultivar | - |
1.14.14.82 | flower | - |
Perilla frutescens | - |
1.14.14.82 | flower | - |
Allium cepa | - |
1.14.14.82 | flower | - |
Arabidopsis thaliana | - |
1.14.14.82 | flower | - |
Gentiana triflora | - |
1.14.14.82 | flower | - |
Glycine max | - |
1.14.14.82 | flower | - |
Ipomoea nil | - |
1.14.14.82 | flower | - |
Pelargonium x hortorum | - |
1.14.14.82 | flower | - |
Petunia x hybrida | - |
1.14.14.82 | flower | - |
Matthiola incana | - |
1.14.14.82 | flower | - |
Torenia hybrid cultivar | - |
1.14.14.82 | flower | - |
Callistephus chinensis | - |
1.14.14.82 | flower | - |
Osteospermum hybrid cultivar | - |
1.14.14.82 | flower | - |
Gerbera hybrid cultivar | - |
1.14.14.82 | flower | - |
Pilosella officinarum | - |
1.14.14.82 | petal | - |
Perilla frutescens | - |
1.14.14.82 | petal | - |
Allium cepa | - |
1.14.14.82 | petal | - |
Arabidopsis thaliana | - |
1.14.14.82 | petal | - |
Gentiana triflora | - |
1.14.14.82 | petal | - |
Glycine max | - |
1.14.14.82 | petal | - |
Ipomoea nil | - |
1.14.14.82 | petal | - |
Pelargonium x hortorum | - |
1.14.14.82 | petal | - |
Petunia x hybrida | - |
1.14.14.82 | petal | - |
Matthiola incana | - |
1.14.14.82 | petal | - |
Torenia hybrid cultivar | - |
1.14.14.82 | petal | - |
Callistephus chinensis | - |
1.14.14.82 | petal | - |
Osteospermum hybrid cultivar | - |
1.14.14.82 | petal | - |
Gerbera hybrid cultivar | - |
1.14.14.82 | petal | - |
Pilosella officinarum | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Petunia x hybrida | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Vinca major | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Pericallis cruenta | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Delphinium grandiflorum | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glycine max | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Gossypium hirsutum | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Nierembergia sp. | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Lycianthes rantonnei | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum melongena | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum tuberosum | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Torenia hybrid cultivar | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glandularia x hybrida | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Callistephus chinensis | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | (2S)-naringenin + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Osteospermum hybrid cultivar | (2S)-5,7,3',4',5'-pentahydroxyflavanone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Petunia x hybrida | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Vinca major | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Pericallis cruenta | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Delphinium grandiflorum | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Glycine max | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Gossypium hirsutum | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Nierembergia sp. | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Lycianthes rantonnei | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Solanum melongena | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Solanum tuberosum | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Torenia hybrid cultivar | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Glandularia x hybrida | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Callistephus chinensis | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Osteospermum hybrid cultivar | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Petunia x hybrida | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Vinca major | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Pericallis cruenta | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Delphinium grandiflorum | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glycine max | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Gossypium hirsutum | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Nierembergia sp. | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Lycianthes rantonnei | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum melongena | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum tuberosum | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Torenia hybrid cultivar | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glandularia x hybrida | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Callistephus chinensis | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Osteospermum hybrid cultivar | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Petunia x hybrida | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Vinca major | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Pericallis cruenta | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Delphinium grandiflorum | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glycine max | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Gossypium hirsutum | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Nierembergia sp. | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Lycianthes rantonnei | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum melongena | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum tuberosum | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Torenia hybrid cultivar | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glandularia x hybrida | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Callistephus chinensis | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Osteospermum hybrid cultivar | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Petunia x hybrida | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Vinca major | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Pericallis cruenta | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Delphinium grandiflorum | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Glycine max | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Gossypium hirsutum | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Nierembergia sp. | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Lycianthes rantonnei | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Solanum melongena | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Solanum tuberosum | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Torenia hybrid cultivar | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Glandularia x hybrida | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Callistephus chinensis | ? | - |
? | |
1.14.14.81 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Osteospermum hybrid cultivar | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Petunia x hybrida | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Pericallis cruenta | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Delphinium grandiflorum | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Glycine max | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Gossypium hirsutum | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Nierembergia sp. | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Lycianthes rantonnei | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Solanum melongena | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Solanum tuberosum | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Torenia hybrid cultivar | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Glandularia x hybrida | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Callistephus chinensis | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, 3',5'-hydroxylation, 3',4'-hydroxylation and 3',4',5'-hydroxylation occurs, overview | Osteospermum hybrid cultivar | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, overview | Vinca major | ? | - |
? | |
1.14.14.81 | additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, overview | Glycine max | ? | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Perilla frutescens | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Allium cepa | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Arabidopsis thaliana | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Gentiana triflora | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Glycine max | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Ipomoea nil | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Pelargonium x hortorum | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Petunia x hybrida | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Matthiola incana | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Torenia hybrid cultivar | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Callistephus chinensis | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Osteospermum hybrid cultivar | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Gerbera hybrid cultivar | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 | - |
Pilosella officinarum | dihydroquercetin + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Perilla frutescens | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Allium cepa | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Arabidopsis thaliana | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Gentiana triflora | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Glycine max | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Ipomoea nil | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Pelargonium x hortorum | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Petunia x hybrida | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Matthiola incana | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Torenia hybrid cultivar | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Callistephus chinensis | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Osteospermum hybrid cultivar | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Gerbera hybrid cultivar | ? | - |
? | |
1.14.14.82 | additional information | the hydroxylation pattern of the B-ring of flavonoids is determined by the activity of the flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase, phylogenetic analysis of sequences of both enzymes indicate that F3',5'H is recruited from F3'H before the divergence of angiosperms and gymnosperms, flavonoid biosynthesis pathways, overview | Pilosella officinarum | ? | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Perilla frutescens | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Allium cepa | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Arabidopsis thaliana | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Gentiana triflora | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Glycine max | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Ipomoea nil | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Pelargonium x hortorum | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Petunia x hybrida | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Matthiola incana | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Torenia hybrid cultivar | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Callistephus chinensis | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Osteospermum hybrid cultivar | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Gerbera hybrid cultivar | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
1.14.14.82 | naringenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Pilosella officinarum | eriodictyol + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
1.14.14.81 | F3',5'H | - |
Petunia x hybrida |
1.14.14.81 | F3',5'H | - |
Vinca major |
1.14.14.81 | F3',5'H | - |
Pericallis cruenta |
1.14.14.81 | F3',5'H | - |
Delphinium grandiflorum |
1.14.14.81 | F3',5'H | - |
Glycine max |
1.14.14.81 | F3',5'H | - |
Gossypium hirsutum |
1.14.14.81 | F3',5'H | - |
Nierembergia sp. |
1.14.14.81 | F3',5'H | - |
Lycianthes rantonnei |
1.14.14.81 | F3',5'H | - |
Solanum melongena |
1.14.14.81 | F3',5'H | - |
Solanum tuberosum |
1.14.14.81 | F3',5'H | - |
Torenia hybrid cultivar |
1.14.14.81 | F3',5'H | - |
Glandularia x hybrida |
1.14.14.81 | F3',5'H | - |
Callistephus chinensis |
1.14.14.81 | F3',5'H | - |
Osteospermum hybrid cultivar |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Petunia x hybrida |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Vinca major |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Pericallis cruenta |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Delphinium grandiflorum |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Glycine max |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Gossypium hirsutum |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Nierembergia sp. |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Lycianthes rantonnei |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Solanum melongena |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Solanum tuberosum |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Torenia hybrid cultivar |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Glandularia x hybrida |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Callistephus chinensis |
1.14.14.81 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Osteospermum hybrid cultivar |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Perilla frutescens |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Allium cepa |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Arabidopsis thaliana |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Gentiana triflora |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Glycine max |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Ipomoea nil |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Pelargonium x hortorum |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Petunia x hybrida |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Matthiola incana |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Torenia hybrid cultivar |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Callistephus chinensis |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Osteospermum hybrid cultivar |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Gerbera hybrid cultivar |
1.14.14.82 | flavonoid 3'-hydroxylase | - |
Pilosella officinarum |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Perilla frutescens |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Allium cepa |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Arabidopsis thaliana |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Gentiana triflora |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Glycine max |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Ipomoea nil |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Pelargonium x hortorum |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Petunia x hybrida |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Matthiola incana |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Torenia hybrid cultivar |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Callistephus chinensis |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Osteospermum hybrid cultivar |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Gerbera hybrid cultivar |
1.14.14.82 | More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Pilosella officinarum |
EC Number | Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|---|
1.14.14.81 | 30 | - |
assay at | Petunia x hybrida |
1.14.14.81 | 30 | - |
assay at | Vinca major |
1.14.14.81 | 30 | - |
assay at | Pericallis cruenta |
1.14.14.81 | 30 | - |
assay at | Delphinium grandiflorum |
1.14.14.81 | 30 | - |
assay at | Glycine max |
1.14.14.81 | 30 | - |
assay at | Gossypium hirsutum |
1.14.14.81 | 30 | - |
assay at | Nierembergia sp. |
1.14.14.81 | 30 | - |
assay at | Lycianthes rantonnei |
1.14.14.81 | 30 | - |
assay at | Solanum melongena |
1.14.14.81 | 30 | - |
assay at | Solanum tuberosum |
1.14.14.81 | 30 | - |
assay at | Torenia hybrid cultivar |
1.14.14.81 | 30 | - |
assay at | Glandularia x hybrida |
1.14.14.81 | 30 | - |
assay at | Callistephus chinensis |
1.14.14.81 | 30 | - |
assay at | Osteospermum hybrid cultivar |
1.14.14.82 | 30 | - |
assay at | Perilla frutescens |
1.14.14.82 | 30 | - |
assay at | Allium cepa |
1.14.14.82 | 30 | - |
assay at | Arabidopsis thaliana |
1.14.14.82 | 30 | - |
assay at | Gentiana triflora |
1.14.14.82 | 30 | - |
assay at | Glycine max |
1.14.14.82 | 30 | - |
assay at | Ipomoea nil |
1.14.14.82 | 30 | - |
assay at | Pelargonium x hortorum |
1.14.14.82 | 30 | - |
assay at | Petunia x hybrida |
1.14.14.82 | 30 | - |
assay at | Matthiola incana |
1.14.14.82 | 30 | - |
assay at | Torenia hybrid cultivar |
1.14.14.82 | 30 | - |
assay at | Callistephus chinensis |
1.14.14.82 | 30 | - |
assay at | Osteospermum hybrid cultivar |
1.14.14.82 | 30 | - |
assay at | Gerbera hybrid cultivar |
1.14.14.82 | 30 | - |
assay at | Pilosella officinarum |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
1.14.14.81 | 7.5 | - |
assay at | Petunia x hybrida |
1.14.14.81 | 7.5 | - |
assay at | Vinca major |
1.14.14.81 | 7.5 | - |
assay at | Pericallis cruenta |
1.14.14.81 | 7.5 | - |
assay at | Delphinium grandiflorum |
1.14.14.81 | 7.5 | - |
assay at | Glycine max |
1.14.14.81 | 7.5 | - |
assay at | Gossypium hirsutum |
1.14.14.81 | 7.5 | - |
assay at | Nierembergia sp. |
1.14.14.81 | 7.5 | - |
assay at | Lycianthes rantonnei |
1.14.14.81 | 7.5 | - |
assay at | Solanum melongena |
1.14.14.81 | 7.5 | - |
assay at | Solanum tuberosum |
1.14.14.81 | 7.5 | - |
assay at | Torenia hybrid cultivar |
1.14.14.81 | 7.5 | - |
assay at | Glandularia x hybrida |
1.14.14.81 | 7.5 | - |
assay at | Callistephus chinensis |
1.14.14.81 | 7.5 | - |
assay at | Osteospermum hybrid cultivar |
1.14.14.82 | 7.5 | - |
assay at | Perilla frutescens |
1.14.14.82 | 7.5 | - |
assay at | Allium cepa |
1.14.14.82 | 7.5 | - |
assay at | Arabidopsis thaliana |
1.14.14.82 | 7.5 | - |
assay at | Gentiana triflora |
1.14.14.82 | 7.5 | - |
assay at | Glycine max |
1.14.14.82 | 7.5 | - |
assay at | Ipomoea nil |
1.14.14.82 | 7.5 | - |
assay at | Pelargonium x hortorum |
1.14.14.82 | 7.5 | - |
assay at | Petunia x hybrida |
1.14.14.82 | 7.5 | - |
assay at | Matthiola incana |
1.14.14.82 | 7.5 | - |
assay at | Torenia hybrid cultivar |
1.14.14.82 | 7.5 | - |
assay at | Callistephus chinensis |
1.14.14.82 | 7.5 | - |
assay at | Osteospermum hybrid cultivar |
1.14.14.82 | 7.5 | - |
assay at | Gerbera hybrid cultivar |
1.14.14.82 | 7.5 | - |
assay at | Pilosella officinarum |