Detail Information

P450 Protein:

P450 SymbolCYP105A3
Protein NameCytochrome P450 105A3
Uniprot IDQ59831
EC Number1.14.-.-
SpeciesStreptomyces carbophilus
Txid 44059
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 C23H34O5 → C23H36O7
Reaction TypeOxidation
Chemical BondCH3

Mevastatin

CYP105A3

Pravastatin

Substrate Information:

Substrate Name Mevastatin
Substrate Chemical FormulaC23H34O5
Substrate PubChem CID64715
Substrate SmilesCC[C@H](C)C(=O)O[C@H]1CCC=C2[C@H]1[C@H]([C@H](C=C2)C)CC[C@@H]3C[C@H](CC(=O)O3)O
Substrate Structure

Product Information:

Product Name Pravastatin
Product Chemical FormulaC23H36O7
Product PubChem CID54687
Product SmilesCC[C@H](C)C(=O)O[C@H]1C[C@@H](C=C2[C@H]1[C@H]([C@H](C=C2)C)CC[C@H](C[C@H](CC(=O)O)O)O)O
Product Structure

References:

Title: A two component-type cytochrome P-450 monooxygenase system in a prokaryote that catalyzes hydroxylation of ML-236B to pravastatin, a tissue-selective inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase.
PMID: 1905157
Journal: Biochimica et biophysica acta
Year: 1991/6/19
Title: Cloning, characterization and expression of the gene encoding cytochrome P-450sca-2 from Streptomyces carbophilus involved in production of pravastatin, a specific HMG-CoA reductase inhibitor.
PMID: 7557483
Journal: Gene
Year: 1995/9/22

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