P450 Protein:
| P450 Symbol | OxyA |
| Protein Name | OxyA |
| Uniprot ID | A0A385L3H5 |
| 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 | C88H103Cl2N9O33 → C88H101Cl2N9O33 |
| Reaction Type | Oxidation |
| Chemical Bond | C-O |
OxyA
Substrate Information:
| Substrate Name | / |
| Substrate Chemical Formula | C88H103Cl2N9O33 |
| Substrate Smiles | CCCCCCCCCC(N[C@H]1[C@H](OC2=C(O)C=C([C@@H](NC([C@H]3NC(=O)[C@@H](CC4C=CC(O)=C(Cl)C=4)NC(=O)[C@H](N)C4=CC(=C(O)C=C4)OC4=CC3=CC(O)=C4)=O)C(=O)N[C@@H](C(N[C@H](C(N[C@H](C(O)=O)C3C=C(O)C=C(OC4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O)C=3)=O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3NC(C)=O)C3C=CC=C(Cl)C=3)=O)C3=CC=C(O)C=C3)C=C2)O[C@H](CO)[C@@H](O)[C@@H]1O)=O |
| Substrate Structure |
Product Information:
| Product Name | / |
| Product Chemical Formula | C88H101Cl2N9O33 |
| Product Smiles | CCCCCCCCCC(N[C@H]1[C@H](OC2=C(O)C=C3[C@@H](NC([C@H]4NC(=O)[C@@H](CC5C=CC(OC2=C3)=C(Cl)C=5)NC(=O)[C@H](N)C2=CC(=C(O)C=C2)OC2=CC4=CC(O)=C2)=O)C(=O)N[C@@H](C(N[C@H](C(N[C@H](C(O)=O)C2C=C(O)C=C(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]3O)C=2)=O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2NC(C)=O)C2C=CC=C(Cl)C=2)=O)C2=CC=C(O)C=C2)O[C@H](CO)[C@@H](O)[C@@H]1O)=O |
| Product Structure |
References:
| Title: | Radical enzymatic peptide cyclization in natural product biosynthesis |
| PMID: | 41697225 |
| Journal: | Chemical Society reviews |
| Year: | 2026/3/9 |