Detail Information

P450 Protein:

P450 SymbolCYP75B137
Protein NameFlavonoid 3'-monooxygenase CYP75B137
Uniprot IDA0A4D6Q415
EC Number1.14.14.82
SpeciesCrocosmia x crocosmiiflora (Montbretia) (Crocosmia aurea x Crocosmia pottsii)
Txid 1053288
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
Subcellular LocationMembrane; Single-pass membrane protein
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C15HO2R9 + C17H21N4O9P-2 + O2 → C15HO3R9 + C17H18N4O9P-3 + H2O + H+
Reaction TypeOxidation
Chemical BondCH
RheaID 16337

A 3′-Unsubstituted Flavone

+

FMNH2

+

O2

CYP75B137

A 3′-Hydroxyflavone

+

FMN

+

H2O

+

H+

Substrate Information:

Substrate Name A 3′-Unsubstituted Flavone
Substrate Chemical FormulaC15HO2R9
Substrate PubChem SID85338425
Substrate SmilesC1(=C(C(=C(C2=C1OC(=C(C2=O)*)C3=C(C(=C(C(=C3*)*)*)[H])*)*)*)*)*
Substrate Structure
Substrate Name FMNH2
Substrate Chemical FormulaC17H21N4O9P-2
Substrate PubChem CID44229161
Substrate SmilesCC1=CC2=C(C=C1C)N(C3=C(N2)C(=O)NC(=O)N3)C[C@@H]([C@@H]([C@@H](COP(=O)([O-])[O-])O)O)O
Substrate Structure
Substrate Name O2
Substrate Chemical FormulaO2
Substrate PubChem CID977
Substrate CAS Number7782-44-7
Substrate SmilesO=O
Substrate Structure

Product Information:

Product Name A 3′-Hydroxyflavone
Product Chemical FormulaC15HO3R9
Product PubChem SID162012076
Product SmilesOc1c([*])c([*])c([*])c(c1[*])-c1oc2c([*])c([*])c([*])c([*])c2c(=O)c1[*]
Product Structure
Product Name FMN
Product Chemical FormulaC17H18N4O9P-3
Product PubChem CID44229199
Product SmilesCC1=CC2=C(C=C1C)N(C3=NC(=NC(=O)C3=N2)[O-])C[C@@H]([C@@H]([C@@H](COP(=O)([O-])[O-])O)O)O
Product Structure
Product Name H2O
Product Chemical FormulaH2O
Product PubChem CID962
Product CAS Number7732-18-5
Product SmilesO
Product Structure
Product Name H+
Product Chemical FormulaH+
Product PubChem CID1038
Product CAS Number12408-02-5
Product Smiles[H+]
Product Structure

References:

Title: Flavonol Biosynthesis Genes and Their Use in Engineering the Plant Antidiabetic Metabolite Montbretin A.
PMID: 31004005
Journal: Plant physiology
Year: 2019/7/1

Contact zhy1001@alu.uestc.edu.cn or yangzhang@cdutcm.edu.cn
© Department of Bioinformatics