Detail Information

P450 Protein:

P450 SymbolCYP90C1
Protein Name3-epi-6-deoxocathasterone 23-monooxygenase CYP90C1
Uniprot IDQ9M066
EC Number1.14.14.-; 1.14.14.147
Gene ID 829790
SpeciesArabidopsis thaliana (Mouse-ear cress)
Txid 3702
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
Subcellular LocationEndoplasmic reticulum membrane; Single-pass membrane protein
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C28H48O3 → C28H48O4
Reaction TypeOxidation
Chemical BondCH2

Cathasterone

CYP90C1

Teasterone

Substrate Information:

Substrate Name Cathasterone
Substrate Chemical FormulaC28H48O3
Substrate PubChem CID15341086
Substrate SmilesC[C@H](C[C@@H]([C@@H](C)[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)O)C(C)C
Substrate Structure

Product Information:

Product Name Teasterone
Product Chemical FormulaC28H48O4
Product PubChem CID13475125
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(CC[C@@H](C4)O)C)C)[C@H]([C@@H]([C@@H](C)C(C)C)O)O
Product Structure

References:

Title: C-23 hydroxylation by Arabidopsis CYP90C1 and CYP90D1 reveals a novel shortcut in brassinosteroid biosynthesis.
PMID: 17138693
Journal: The Plant cell
Year: 2006/11/1

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