CYP81F2

Erysimum cheiranthoides CYP81F

Brassicaceae

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

Substrate

indol-3-ylmethyl glucosinolate

PubChem ↗ C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)S[C@H]3[C@@H]([C@H]([C@@H…

CYP81F2

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

4-hydroxy-indol-3-ylmethyl glucosinolate

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 ation; ation; Homolog identified in E. cheiranthoides genome; pathway inferred from Arabidopsis.

Reaction & quality gates

Mechanism: Hydroxylation
Evidence type: Pathway_inference
Confidence: Medium
Data tier: Bronze
evidence=Pathway_inference
Substrate class: Glucosinolates
Product class: Glucosinolates

Literature & public identifiers

PubMed: PMID:32252891 ↗
DOI: 10.7554/elife.51712 ↗
UniProt: C3W7I0 ↗
GenBank: —
NCBI TaxID: 330168 ↗

Independent evolution of ancestral and novel defenses in a genus of toxic plants (<i>Erysimum</i>, Brassicaceae).