UGT78D1

Morus alba

Moraceae

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

Substrate

quercetin 3-O-glucoside

PubChem ↗ C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H](…

UGT78D1

ΔMass: +146.0579 Da mismatch

Product

rutin

PubChem ↗ C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([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; MaUGT78D1 is a flavonol-3-O-glucoside-L-rhamnosyltransferase; speculated to be involved in rutin biosynthesis.

Reaction & quality gates

Mechanism: Glycosylation
Evidence type: Pathway_inference
Confidence: High
Data tier: Quarantine
non-CYP auxiliary enzyme (pathway partner, not cytochrome P450)
Substrate class: Phenylpropanoids
Product class: Other

Literature & public identifiers

PubMed: PMID:38014901 ↗
DOI: 10.1080/15592324.2023.2287881 ↗
UniProt: Q9S9P6 ↗
GenBank: —
NCBI TaxID: 3498 ↗

Biosynthetic pathways and related genes regulation of bioactive ingredients in mulberry leaves.