FsoA

Unknown

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

Substrate

2α-acetyloxy-fern-9(11)-en-3β-ol

PubChem ↗ Crowdsource substrate structure

FsoA

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

(2α,3β)-2-acetyloxy-fern-9(11)-en-3-yl β-D-glucopyranoside

PubChem ↗ [H][C@@]1(O[C@H]2C[C@]3(C)CC[C@]4(C)C(=CC=C5[C@@]6(C)C[C@@H](O)…

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; GT domain of FsoA transfers glucose to 3-OH after acetylation; product 8 confirmed by feeding experiments (Figure 5B).

Reaction & quality gates

Mechanism: Glycosylation
Evidence type: In vivo
Confidence: High
Data tier: Bronze
source_organism 为空
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:40898010 ↗
DOI: 10.1002/advs.202507531 ↗
UniProt: —
GenBank: —
NCBI TaxID: —

Engineered Fusion Enzyme-Mediated Non-Consecutive Cyclization-Glycosylation Enables Heterologous Synthesis of Antifungal Enfumafungin.