OBH

Unknown CYP98A

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping

Substrate

ligupurpuroside B

PubChem ↗ C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@H]2[C@@H](O[C@H]([C@@H]…

OBH

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

ligurobustoside N

PubChem ↗ C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@H]2[C@@H](O[C@H]([C@@H]…

Evidence trail

Excerpts are machine-extracted plain text for biochemical provenance. Follow DOI / PubMed links for the primary literature; publisher figures and PDF images are not displayed here.

Source text excerpt ation; ation; OeCYP98A167 catalyzes same reaction.

Reaction & quality gates

Mechanism: Hydroxylation (+15.99 Da)
Evidence type: In vitro
Confidence: High
Data tier: Quarantine
non-CYP auxiliary enzyme (pathway partner, not cytochrome P450)
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:36935606 ↗
DOI: 10.1016/j.xplc.2023.100592 ↗
UniProt: —
GenBank: —
NCBI TaxID: —

Complete biosynthesis of the phenylethanoid glycoside verbascoside.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme