Detail Information
P450 Protein:
| P450 Symbol | CYP101A1 |
| Protein Name | Camphor 5-monooxygenase |
| Uniprot ID | P00183 |
| EC Number | 1.14.15.1 |
| Gene ID | 9617760 |
| Species | Pseudomonas putida |
| Txid | 303 |
| 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 | C9H10 → C9H10O |
| Reaction Type | Oxidation |
| Chemical Bond | C=C |
CYP101A1
Substrate Information:
| Substrate Name | cis-beta-Methylstyrene |
| Substrate Chemical Formula | C9H10 |
| Substrate PubChem CID | 252324 |
| Substrate Smiles | C=1C=CC(=CC1)C=CC |
| Substrate Structure |
Product Information:
| Product Name | (2R,3S)-2-Methyl-3-phenyloxirane |
| Product Chemical Formula | C9H10O |
| Product PubChem CID | 6452030 |
| Product CAS Number | 14212-53-4 |
| Product Smiles | CC1C(O1)C2=CC=CC=C2 |
| Product Structure |
References:
| Title: | Theoretical and experimental analysis of the absolute stereochemistry of cis-.beta.-methylstyrene epoxidation by cytochrome P450cam |
| DOI: | https://doi.org/10.1021/ja00008a071 |
| Journal: | Journal of the American Chemical Society |
| Year: | 1991/4/1 |