Detail Information

P450 Protein:

P450 SymbolCYP92A
Protein NameCytochrome P450
Uniprot IDQ0PNH1
SpeciesCapsicum chinense (Scotch bonnet) (Bonnet pepper)
Txid 80379
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
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Subcellular Location/
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C28H48O4 → C28H48O5
Reaction TypeOxidation
Chemical BondCH2

Typhasterol

CYP92A

Castasterone

Substrate Information:

Substrate Name Typhasterol
Substrate Chemical FormulaC28H48O4
Substrate PubChem CID13475120
Substrate SmilesC[C@@H]([C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC(=O)[C@@H]4[C@@]3(CC[C@H](C4)O)C)C)[C@H]([C@@H]([C@@H](C)C(C)C)O)O
Substrate Structure

Product Information:

Product Name Castasterone
Product Chemical FormulaC28H48O5
Product PubChem CID133534
Product SmilesC[C@@H]([C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC(=O)[C@@H]4[C@@]3(C[C@H]([C@H](C4)O)O)C)C)[C@H]([C@@H]([C@@H](C)C(C)C)O)O
Product Structure

References:

Title: Cytochrome P450-catalyzed brassinosteroid pathway activation through synthesis of castasterone and brassinolide in Phaseolus vulgaris.
PMID: 15016564
Journal: Phytochemistry
Year: 2004/3/1

Contact zhy1001@alu.uestc.edu.cn or yangzhang@cdutcm.edu.cn
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