Detail Information

P450 Protein:

P450 SymbolcotB3
Protein NameCyclooctat-9-en-7-ol 5-monooxygenase (EC 1.14.99.61)
Uniprot IDC9K1X6
EC Number1.14.99.61
SpeciesStreptomyces melanosporofaciens
Txid 67327
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
Subcellular Location
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C20H34O + RH2 + O2 → C20H34O2 + R + H2O
Reaction TypeOxidation
Chemical BondCH
RheaID 56820

cyclooctat-9-en-7-ol

+

AH2

+

O2

cotB3

cyclooctat-9-ene-5,7-diol

+

A

+

H2O

Substrate Information:

Substrate Name cyclooctat-9-en-7-ol
Substrate Chemical FormulaC20H34O
Substrate PubChem CID132282046
Substrate SmilesCC1CCC2C1CC3(CCC(C3=CCC2(C)O)C(C)C)C
Substrate Structure
Substrate Name AH2
Substrate Chemical FormulaRH2
Substrate Smiles*([H])[H]
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 cyclooctat-9-ene-5,7-diol
Product Chemical FormulaC20H34O2
Product PubChem CID90658403
Product SmilesCC1CC(C2C1CC3(CCC(C3=CCC2(C)O)C(C)C)C)O
Product Structure
Product Name A
Product Chemical FormulaR
Product Smiles*
Product Structure
Product Name H2O
Product Chemical FormulaH2O
Product PubChem CID962
Product CAS Number7732-18-5
Product SmilesO
Product Structure

References:

Title: Cloning and heterologous expression of the cyclooctatin biosynthetic gene cluster afford a diterpene cyclase and two p450 hydroxylases.
PMID: 19635410
Journal: Microbial cell factories
Year: 2009/7/31
Title: Identification, characterization and molecular adaptation of class I redox systems for the production of hydroxylated diterpenoids.
PMID: 27216162
Journal: Chemistry & biology
Year: 2016/5/23

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