Detail Information

P450 Protein:

P450 SymbolAurH
Protein NamePutative cytochrome P450
Uniprot IDQ70KH6
EC Number1.14.15.37
Gene ID 66737957
SpeciesStreptomyces thioluteus
Txid 66431
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 C22H25NO5 → C22H25NO6
Reaction TypeOxidation
Chemical BondCH2
SolventsDimethyl sulfoxide, Water
Conditions5 d, pH 7.4, 30°C
TransformationsHydroxylation at Aliphatic Carbon

6-[(3E,5E)-3,5-Dimethyl-6-(4-nitrophenyl)-3,5-hexadien-1-yl]-4-methoxy-3,5-dimethyl-2H-pyran-2-one

AurH

6-[(1R,3E,5E)-1-Hydroxy-3,5-dimethyl-6-(4-nitrophenyl)-3,5-hexadien-1-yl]-4-methoxy-3,5-dimethyl-2H-pyran-2-one

Substrate Information:

Substrate Name 6-[(3E,5E)-3,5-Dimethyl-6-(4-nitrophenyl)-3,5-hexadien-1-yl]-4-methoxy-3,5-dimethyl-2H-pyran-2-one
Substrate Chemical FormulaC22H25NO5
Substrate PubChem CID46910703
Substrate SmilesO=C1OC(=C(C(OC)=C1C)C)CCC(=CC(=CC2=CC=C(C=C2)N(=O)=O)C)C
Substrate Structure

Product Information:

Product Name 6-[(1R,3E,5E)-1-Hydroxy-3,5-dimethyl-6-(4-nitrophenyl)-3,5-hexadien-1-yl]-4-methoxy-3,5-dimethyl-2H-pyran-2-one
Product Chemical FormulaC22H25NO6
Product PubChem CID46910704
Product CAS Number1239914-05-6
Product SmilesO=C1OC(=C(C(OC)=C1C)C)C(O)CC(=CC(=CC2=CC=C(C=C2)N(=O)=O)C)C
Product Structure

References:

Title: Exploiting enzymatic promiscuity to engineer a focused library of highly selective antifungal and antiproliferative aureothin analogues.
PMID: 20662518
Journal: Journal of the American Chemical Society
Year: 2010/6/13

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