Detail Information

P450 Protein:

P450 SymbolCYP88A108
Protein Name7,8-epoxymelianol synthase CYP88A108
Uniprot IDA0A5B8ND22
EC Number1.14.14.-
SpeciesMelia azedarach
Txid 155640
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 C31H50O2 → C31H48O2
Reaction TypeOxidation
Chemical BondC-OH

11Alpha-hydroxy-beta-amyrin

CYP88A108

11-Oxo-beta-amyrin

Substrate Information:

Substrate Name 11Alpha-hydroxy-beta-amyrin
Substrate Chemical FormulaC31H50O2
Substrate Smiles[C@](C)12CC[C@H](O)[C@](C)(C=C)[C@]1([H])CC[C@@](C)1[C@]2([H])[C@H](O)C=C2[C@@]([H])3C[C@@](C)(CC[C@@]3(CC[C@@]12C)C)C
Substrate Structure

Product Information:

Product Name 11-Oxo-beta-amyrin
Product Chemical FormulaC31H48O2
Product Smiles[C@](C)12CC[C@H](O)[C@](C)(C=C)[C@]1([H])CC[C@@](C)1[C@]2([H])C(=O)C=C2[C@@]([H])3C[C@@](C)(CC[C@@]3(CC[C@@]12C)C)C
Product Structure

References:

Title: Three cytochrome P450 88A subfamily enzymes, CYP88A108, CYP88A164, and CYP88A222, act as β-amyrin 11-oxidases involved in triterpenoid biosynthesis in Melia azedarach L.
PMID: 40541870
Journal: International Journal of Biological Macromolecule
Year: 2025/6/18

Contact zhy1001@alu.uestc.edu.cn or yangzhang@cdutcm.edu.cn
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