Detail Information

P450 Protein:

P450 SymbolOxyB
Protein NameOxyB
Uniprot IDA0A385L3H2
SpeciesAmycolatopsis 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 C88H101Cl2N9O33 → C88H99Cl2N9O33
Reaction TypeOxidation
Chemical BondC-O

/

OxyB

/

Substrate Information:

Substrate Name /
Substrate Chemical FormulaC88H101Cl2N9O33
Substrate SmilesCCCCCCCCCC(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
Substrate Structure

Product Information:

Product Name /
Product Chemical FormulaC88H99Cl2N9O33
Product SmilesCCCCCCCCCC(N[C@H]1[C@H](OC2=C3OC4C=CC([C@@H](O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5NC(C)=O)[C@H](NC(=O)[C@H](NC([C@H]5C(=C3)C=C2OC2C=CC(=CC=2Cl)C[C@@H]2C(N[C@@H](C3C=C(OC6C=C([C@@H](N)C(N2)=O)C=CC=6O)C=C(O)C=3)C(=O)N5)=O)=O)C2=CC=C(O)C=C2)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)=CC=4Cl)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

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