Detail Information

P450 Protein:

P450 SymbolbezE
Protein NameCytochrome P450 monooxygenase
Uniprot IDA0A2Z5X755
SpeciesStreptomyces sp. RI18
Txid 1894972
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 C20H27NO5 → C18H24ClNO3
Reaction TypeCyclization
Chemical BondC=C

4-(acetoxyamino)-3-[(2Z)-3-(hydroxymethyl)-6,7-dimethylocta-2,6-dienyl]benzoic acid

bezE

(2R,3R)-3-chloro-2-(3,4-dimethylpent-3-enyl)-2-(hydroxymethyl)-1,2,3,4-tetrahydroquinoline-6-carboxylic acid

Substrate Information:

Substrate Name 4-(acetoxyamino)-3-[(2Z)-3-(hydroxymethyl)-6,7-dimethylocta-2,6-dienyl]benzoic acid
Substrate Chemical FormulaC20H27NO5
Substrate SmilesO=C(C)ONC1=C(C=C(C=C1)C(O)=O)C/C=C(CO)/CC/C(=C(C)/C)/C
Substrate Structure

Product Information:

Product Name (2R,3R)-3-chloro-2-(3,4-dimethylpent-3-enyl)-2-(hydroxymethyl)-1,2,3,4-tetrahydroquinoline-6-carboxylic acid
Product Chemical FormulaC18H24ClNO3
Product SmilesOC(C1=CC=C2C(=C1)C[C@@H](Cl)[C@](CO)(CC/C(/C)=C(C)/C)N2)=O
Product Structure

References:

Title: Unprecedented Cyclization Catalyzed by a Cytochrome P450 in Benzastatin Biosynthesis.
PMID: 29716187
Journal: Journal of the American Chemical Society
Year: 2018/5/2

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