BcUGT009

Belamcanda chinensis

Iridaceae

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

Substrate

iristectorigenin B

PubChem ↗ COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O)O

BcUGT009

ΔMass: +162.0528 Da mismatch

Product

iristectorin B

PubChem ↗ COC1=C(C=CC(=C1)C2=COC3=CC(=C(C(=C3C2=O)O)OC)O[C@H]4[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; 7-O-glucosylation; kinetic data provided.

Reaction & quality gates

Mechanism: Glycosylation
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:41830405 ↗
DOI: 10.1111/pbi.70612 ↗
UniProt: —
GenBank: —
NCBI TaxID: 58944 ↗

A Near Telomere-to-Telomere Genome of Belamcanda chinensis Provides Insights Into Genome Evolution and the Biosynthesis of Characteristic Isoflavones.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme