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 | C10H16 → C10H16O + C10H16O |
| Reaction Type | Oxidation |
| Chemical Bond | CH |
| Solvents | Water |
| Transformations | 1. Hydroxylation at an Aliphatic Carbon |
CYP101A1
Substrate Information:
| Substrate Name | Adamantane |
| Substrate Chemical Formula | C10H16 |
| Substrate PubChem CID | 9238 |
| Substrate Smiles | C1C2CC3CC1CC(C2)C3 |
| Substrate Structure |
Product Information:
| Product Name | 1-Adamantanol |
| Product Chemical Formula | C10H16O |
| Product PubChem CID | 64152 |
| Product CAS Number | 768-95-6 |
| Product Smiles | C1C2CC3CC1CC(C2)(C3)O |
| Product Structure |
| Product Name | 2-Adamantanol |
| Product Chemical Formula | C10H16O |
| Product PubChem CID | 64149 |
| Product CAS Number | 700-57-2 |
| Product Smiles | C1C2CC3CC1CC(C2)C3O |
| Product Structure |
References:
| Title: | Regioselective hydroxylation of adamantane by Streptomyces griseoplanus cells. |
| PMID: | 16187097 |
| Journal: | Applied Microbiology and Biotechnology (2006) |
| Year: | 2005/9/27 |