Detail Information

P450 Protein:

P450 SymbolCYP716S1
Protein NameProtopanaxadiol 6-hydroxylase
Uniprot IDI7CT85
EC Number1.14.14.121
SpeciesPanax ginseng (Korean ginseng)
Txid 4054
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
Subcellular LocationMembrane; Single-pass membrane protein
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C30H52O3 → C30H52O4
Reaction TypeOxidation
Chemical BondCH3

Protopanaxadiol

CYP716S1

Protopanaxatriol

Substrate Information:

Substrate Name Protopanaxadiol
Substrate Chemical FormulaC30H52O3
Substrate PubChem CID9920281
Substrate SmilesCC(=CCC[C@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)O)C)O)C
Substrate Structure

Product Information:

Product Name Protopanaxatriol
Product Chemical FormulaC30H52O4
Product PubChem CID9847853
Product SmilesCC(=CCC[C@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(C[C@@H]([C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)O)C)O)C)O)C
Product Structure

References:

Title: Cytochrome P450 CYP716A53v2 catalyzes the formation of protopanaxatriol from protopanaxadiol during ginsenoside biosynthesis in Panax ginseng.
PMID: 22875608
Journal: Plant & cell physiology
Year: 2012/9/1

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