P450 Protein:
| P450 Symbol | OxyB |
| Protein Name | OxyB |
| Uniprot ID | A0A385L3H2 |
| Species | Amycolatopsis keratiniphila |
| Txid | 129921 |
| 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 | C66H77ClN8O24 → C66H75ClN8O24 |
| Reaction Type | Oxidation |
| Chemical Bond | C-O |
OxyB
Substrate Information:
| Substrate Name | / |
| Substrate Chemical Formula | C66H77ClN8O24 |
| Substrate Smiles | C1C=C([C@H](NC(=O)[C@H]([C@H](O)C2=CC=C(C(=C2)Cl)O)NC([C@H](NC([C@H]2C3=CC(OC4=C([*])C=C(C=C4)[C@@H](O)[C@@H](NC([C@H](NC)CC(C)C)=O)C(=O)N[C@@H](CC(=O)N)C(=O)N2)=C(O[C@H]2C(C(O)C(O)[C@@H](CO)O2)O[C@@H]2CC(C)([*])C(O)[C@H](C)O2)C=C3)=O)C2C=CC(O)=CC=2)=O)C(=O)O)C(O)=CC=1O |
| Substrate Structure |
Product Information:
| Product Name | / |
| Product Chemical Formula | C66H75ClN8O24 |
| Product Smiles | C1C=C([C@H](NC(=O)[C@@H]2[C@H](O)C3=CC=C(C(=C3)Cl)OC3=CC4=CC(OC5=C([*])C=C(C=C5)[C@@H](O)[C@@H](NC([C@H](NC)CC(C)C)=O)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@H]4C(=O)N[C@H](C4C=CC(O)=CC=4)C(=O)N2)=C3O[C@H]2C(C(O)C(O)[C@@H](CO)O2)O[C@@H]2CC(C)([*])C(O)[C@H](C)O2)C(=O)O)C(O)=CC=1O |
| Product Structure |
References:
| Title: | Radical enzymatic peptide cyclization in natural product biosynthesis |
| PMID: | 41697225 |
| Journal: | Chemical Society reviews |
| Year: | 2026/3/9 |