Detail Information

P450 Protein:

P450 SymbolCYP152A1
Protein NameP450BSβ-L78I/Q85H/G290I mutation
Uniprot ID
SpeciesBacillus subtilis (strain 168)
Txid 224308
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 C17H33NO4 → C17H33NO5
Reaction TypeOxidation
Chemical BondCH
SolventsEthanol;Polyethylene glycol mono(tert-octylphenyl) ether
Conditions60 min, rt
TransformationsHydroxylation at an Aliphatic Carbon

12-[(2-methylpropan-2-yl)oxycarbonylamino]dodecanoic acid

CYP152A1

(3R)-12-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-hydroxydodecanoic acid

Substrate Information:

Substrate Name 12-[(2-methylpropan-2-yl)oxycarbonylamino]dodecanoic acid
Substrate Chemical FormulaC17H33NO4
Substrate PubChem CID4428132
Substrate SmilesCC(C)(C)OC(=O)NCCCCCCCCCCCC(=O)O
Substrate Structure

Product Information:

Product Name (3R)-12-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-hydroxydodecanoic acid
Product Chemical FormulaC17H33NO5
Product CAS Number2776235-44-8
Product SmilesC(NCCCCCCCCC[C@H](CC(O)=O)O)(OC(C)(C)C)=O
Product Structure

References:

Title: Biocatalytic Enantioselective β-Hydroxylation of Unactivated C-H Bonds in Aliphatic Carboxylic Acids.
PMID: 35536725
Journal: Angewandte Chemie, International Edition
Year: 2022/5/10

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