FsoF

Unknown

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

Substrate

fern-9(11)-ene-2α,3β-diol

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

FsoF

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

2α-acetyloxy-fern-9(11)-en-3β-ol

PubChem ↗ Crowdsource product structure

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 Other; Other; FsoF catalyzes acetylation of 2-OH; product 9 detected in AO-efuA(TC)-fsoD/F (Figure 5A, line iv).

Reaction & quality gates

Mechanism: Other
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.