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Literature summary for 1.14.14.81 extracted from
- Cloning, functional identification and sequence analysis of flavonoid 3'-hydroxylase and flavonoid 3',5'-hydroxylase cDNAs reveals independent evolution of flavonoid 3,5-hydroxylase in the Asteraceae family (2006), Plant Mol. Biol., 61, 365-381.
Cloned(Commentary)
| Cloned (Comment) | Organism |
|---|---|
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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. |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
Localization
| Localization | Comment | Organism | GeneOntology No. | Textmining |
|---|---|---|---|---|
| microsome | - |
Petunia x hybrida | - |
- |
| microsome | - |
Vinca major | - |
- |
| microsome | - |
Pericallis cruenta | - |
- |
| microsome | - |
Delphinium grandiflorum | - |
- |
| microsome | - |
Glycine max | - |
- |
| microsome | - |
Gossypium hirsutum | - |
- |
| microsome | - |
Nierembergia sp. | - |
- |
| microsome | - |
Lycianthes rantonnei | - |
- |
| microsome | - |
Solanum melongena | - |
- |
| microsome | - |
Solanum tuberosum | - |
- |
| microsome | - |
Torenia hybrid cultivar | - |
- |
| microsome | - |
Glandularia x hybrida | - |
- |
| microsome | - |
Callistephus chinensis | - |
- |
| microsome | - |
Osteospermum hybrid cultivar | - |
- |
Natural Substrates/ Products (Substrates)
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 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 | ? | - |
? |  |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Callistephus chinensis | Q9FPN4 | line '01' | - |
| Delphinium grandiflorum | Q52YL8 | - |
- |
| Glandularia x hybrida | Q6J210 | - |
- |
| Glycine max | Q6YLS3 | - |
- |
| Gossypium hirsutum | Q84NG3 | i.e. Gossypium maxicanum | - |
| Lycianthes rantonnei | Q9FPN3 | blue potato bush | - |
| Nierembergia sp. | Q8LP20 | - |
- |
| Osteospermum hybrid cultivar | Q304Q4 | cv. Bamba | - |
| Pericallis cruenta | Q304Q5 | cv. Blue Bicolor | - |
| Petunia x hybrida | P48418 | - |
- |
| Solanum melongena | P37120 | - |
- |
| Solanum tuberosum | Q5EWY2 | - |
- |
| Torenia hybrid cultivar | Q9FS35 | hybrid cultivar | - |
| Vinca major | Q76LL4 | - |
- |
Source Tissue
| Source Tissue | Comment | Organism | Textmining |
|---|---|---|---|
| flower | - |
Petunia x hybrida | - |
| flower | - |
Vinca major | - |
| flower | - |
Pericallis cruenta | - |
| flower | - |
Delphinium grandiflorum | - |
| flower | - |
Glycine max | - |
| flower | - |
Gossypium hirsutum | - |
| flower | - |
Nierembergia sp. | - |
| flower | - |
Lycianthes rantonnei | - |
| flower | - |
Solanum melongena | - |
| flower | - |
Solanum tuberosum | - |
| flower | - |
Torenia hybrid cultivar | - |
| flower | - |
Glandularia x hybrida | - |
| flower | - |
Callistephus chinensis | - |
| flower | - |
Osteospermum hybrid cultivar | - |
| petal | - |
Petunia x hybrida | - |
| petal | - |
Vinca major | - |
| petal | - |
Pericallis cruenta | - |
| petal | - |
Delphinium grandiflorum | - |
| petal | - |
Glycine max | - |
| petal | - |
Gossypium hirsutum | - |
| petal | - |
Nierembergia sp. | - |
| petal | - |
Lycianthes rantonnei | - |
| petal | - |
Solanum melongena | - |
| petal | - |
Solanum tuberosum | - |
| petal | - |
Torenia hybrid cultivar | - |
| petal | - |
Glandularia x hybrida | - |
| petal | - |
Callistephus chinensis | - |
| petal | - |
Osteospermum hybrid cultivar | - |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| (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 | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Petunia x hybrida | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Vinca major | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Pericallis cruenta | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Delphinium grandiflorum | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Glycine max | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Gossypium hirsutum | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Nierembergia sp. | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Lycianthes rantonnei | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Solanum melongena | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Solanum tuberosum | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Torenia hybrid cultivar | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Glandularia x hybrida | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Callistephus chinensis | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| apigenin + [reduced NADPH-hemoprotein reductase] + O2 | - |
Osteospermum hybrid cultivar | 5,7,3',4',5'-pentahydroxyflavone + [oxidized NADPH-hemoprotein reductase] + H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Petunia x hybrida | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Vinca major | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Pericallis cruenta | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Delphinium grandiflorum | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glycine max | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Gossypium hirsutum | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Nierembergia sp. | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Lycianthes rantonnei | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum melongena | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum tuberosum | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Torenia hybrid cultivar | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glandularia x hybrida | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Callistephus chinensis | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Osteospermum hybrid cultivar | dihydromyricetin + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Petunia x hybrida | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Vinca major | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Pericallis cruenta | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Delphinium grandiflorum | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glycine max | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Gossypium hirsutum | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Nierembergia sp. | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Lycianthes rantonnei | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum melongena | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Solanum tuberosum | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Torenia hybrid cultivar | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Glandularia x hybrida | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Callistephus chinensis | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| kaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 | - |
Osteospermum hybrid cultivar | 5,7,3',4',5'-pentahydroxyflavone + 2 [oxidized NADPH-hemoprotein reductase] + 2 H2O | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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. | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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. | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| 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 | ? | - |
? | |
| additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, overview | Vinca major | ? | - |
? | |
| additional information | the enzyme hydroxylates a broad range of flavonoid substrates in vitro, overview | Glycine max | ? | - |
? | |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| F3',5'H | - |
Petunia x hybrida |
| F3',5'H | - |
Vinca major |
| F3',5'H | - |
Pericallis cruenta |
| F3',5'H | - |
Delphinium grandiflorum |
| F3',5'H | - |
Glycine max |
| F3',5'H | - |
Gossypium hirsutum |
| F3',5'H | - |
Nierembergia sp. |
| F3',5'H | - |
Lycianthes rantonnei |
| F3',5'H | - |
Solanum melongena |
| F3',5'H | - |
Solanum tuberosum |
| F3',5'H | - |
Torenia hybrid cultivar |
| F3',5'H | - |
Glandularia x hybrida |
| F3',5'H | - |
Callistephus chinensis |
| F3',5'H | - |
Osteospermum hybrid cultivar |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Petunia x hybrida |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Vinca major |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Pericallis cruenta |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Delphinium grandiflorum |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Glycine max |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Gossypium hirsutum |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Nierembergia sp. |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Lycianthes rantonnei |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Solanum melongena |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Solanum tuberosum |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Torenia hybrid cultivar |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Glandularia x hybrida |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Callistephus chinensis |
| More | the enzyme belongs to the vast and versatile cytochrome P450 protein family of enzymes | Osteospermum hybrid cultivar |
Temperature Optimum [°C]
| Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
|---|---|---|---|
| 30 | - |
assay at | Petunia x hybrida |
| 30 | - |
assay at | Vinca major |
| 30 | - |
assay at | Pericallis cruenta |
| 30 | - |
assay at | Delphinium grandiflorum |
| 30 | - |
assay at | Glycine max |
| 30 | - |
assay at | Gossypium hirsutum |
| 30 | - |
assay at | Nierembergia sp. |
| 30 | - |
assay at | Lycianthes rantonnei |
| 30 | - |
assay at | Solanum melongena |
| 30 | - |
assay at | Solanum tuberosum |
| 30 | - |
assay at | Torenia hybrid cultivar |
| 30 | - |
assay at | Glandularia x hybrida |
| 30 | - |
assay at | Callistephus chinensis |
| 30 | - |
assay at | Osteospermum hybrid cultivar |
pH Optimum
| pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
|---|---|---|---|
| 7.5 | - |
assay at | Petunia x hybrida |
| 7.5 | - |
assay at | Vinca major |
| 7.5 | - |
assay at | Pericallis cruenta |
| 7.5 | - |
assay at | Delphinium grandiflorum |
| 7.5 | - |
assay at | Glycine max |
| 7.5 | - |
assay at | Gossypium hirsutum |
| 7.5 | - |
assay at | Nierembergia sp. |
| 7.5 | - |
assay at | Lycianthes rantonnei |
| 7.5 | - |
assay at | Solanum melongena |
| 7.5 | - |
assay at | Solanum tuberosum |
| 7.5 | - |
assay at | Torenia hybrid cultivar |
| 7.5 | - |
assay at | Glandularia x hybrida |
| 7.5 | - |
assay at | Callistephus chinensis |
| 7.5 | - |
assay at | Osteospermum hybrid cultivar |
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Release 2023.1 (January 2023)
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