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

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

AurH

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

Substrate Information:

Substrate Name 2-[(3E,5E)-3,5-Dimethyl-6-(4-nitrophenyl)-3,5-hexadien-1-yl]-6-methoxy-3,5-dimethyl-4H-pyran-4-one
Substrate Chemical FormulaC22H25NO5
Substrate PubChem CID11246062
Substrate SmilesO=C1C(=C(OC(=C1C)CCC(=CC(=CC2=CC=C(C=C2)N(=O)=O)C)C)OC)C
Substrate Structure

Product Information:

Product Name 2-[(1R,3E,5E)-1-Hydroxy-3,5-dimethyl-6-(4-nitrophenyl)-3,5-hexadien-1-yl]-6-methoxy-3,5-dimethyl-4H-pyran-4-one
Product Chemical FormulaC22H25NO6
Product PubChem CID102027521
Product CAS Number1101168-58-4
Product SmilesO=C1C(=C(OC(=C1C)C(O)CC(=CC(=CC2=CC=C(C=C2)N(=O)=O)C)C)OC)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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