Detail Information

P450 Protein:

P450 SymbolCYP3A4
Protein NameCytochrome P450 3A4
Uniprot IDP08684
EC Number1.14.14.1; 1.14.14.55; 1.14.14.56; 1.14.14.73
Gene ID 1576
SpeciesHomo sapiens (Human)
Txid 9606
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
Subcellular LocationEndoplasmic reticulum membrane; Peripheral membrane protein Microsome membrane; Peripheral membrane protein
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C20H31O2- + C17H21N4O9P-2 + O2 → C20H31O3- + FMN + H2O + H+
Reaction TypeOxidation
Chemical BondCH2
RheaID 52292

(5Z,8Z,11Z,14Z)-Eicosatetraenoate

+

FMNH2

+

O2

CYP3A4

13-Hydroxy-(5Z,8Z,11Z,14Z)-Eicosatetraenoate

+

FMN

+

H2O

+

H+

Substrate Information:

Substrate Name (5Z,8Z,11Z,14Z)-Eicosatetraenoate
Substrate Chemical FormulaC20H31O2-
Substrate PubChem CID5460265
Substrate SmilesCCCCC/C=CC/C=CC/C=CC/C=CCCCC(=O)[O-]
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 13-Hydroxy-(5Z,8Z,11Z,14Z)-Eicosatetraenoate
Product Chemical FormulaC20H31O3-
Product PubChem CID126456465
Product SmilesCCCCC/C=CC(/C=CC/C=CC/C=CCCCC(=O)[O-])O
Product Structure
Product Name FMN
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: Cytochromes P450 with bisallylic hydroxylation activity on arachidonic and linoleic acids studied with human recombinant enzymes and with human and rat liver microsomes.
PMID: 9435160
Journal: The Journal of pharmacology and experimental therapeutics
Year: 1998/1/1

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