Detail Information

P450 Protein:

P450 SymbolCYP5A1
Protein NameThromboxane-A synthase
Uniprot IDP24557
EC Number4.2.1.152; 5.3.99.5
Gene ID 6916
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; Multi-pass membrane protein
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C20H32O5 → C17H27O3- + C3H4O2
Reaction TypeReduction
Chemical BondO-O
RheaID 48644

Prostaglandin H2

CYP5A1

(12S)-Hydroxy-(5Z,8E,10E)-Heptadecatrienoate

+

Malonaldehyde

Substrate Information:

Substrate Name Prostaglandin H2
Substrate Chemical FormulaC20H32O5
Substrate PubChem CID445049
Substrate SmilesCCCCC[C@@H](/C=C/[C@H]1[C@H]2C[C@@H]([C@@H]1C/C=CCCCC(=O)O)OO2)O
Substrate Structure

Product Information:

Product Name (12S)-Hydroxy-(5Z,8E,10E)-Heptadecatrienoate
Product Chemical FormulaC17H27O3-
Product PubChem CID102571778
Product SmilesCCCCC[C@@H](/C=C/C=C/C/C=CCCCC(=O)[O-])O
Product Structure
Product Name Malonaldehyde
Product Chemical FormulaC3H4O2
Product PubChem CID10964
Product SmilesC(C=O)C=O
Product Structure

References:

Title: Substrate binding is the rate-limiting step in thromboxane synthase catalysis.
PMID: 11297515
Journal: The Journal of biological chemistry
Year: 2001/5/4
Title: Functional analysis of human thromboxane synthase polymorphic variants.
PMID: 22735388
Journal: Pharmacogenetics and genomics
Year: 2012/9/1
Title: Expression, purification, and spectroscopic characterization of human thromboxane synthase.
PMID: 9873013
Journal: The Journal of biological chemistry
Year: 1999/1/8

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