CYP90A1

Szekeres et CYP90A

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

Substrate

(22S)-22-hydroxy-campesterol

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

CYP90A1

ΔMass: -2.0157 Da ketone_formation(-2.0157)

Product

(22S,24R)-22-hydroxy-ergost-4-en-3-one

PubChem ↗ C[C@H](C[C@@H]([C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC…

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; CYP90A1 (CPD) catalyzes C3 oxidation; in vitro evidence from Szekeres et al., 1996; Ohnishi et al., 2012.

Reaction & quality gates

Mechanism: Ketone formation (-2.02 Da)
Evidence type: In vitro
Confidence: High
Data tier: Gold
Latin binomial + experiment + dual SMILES + ΔMass pass
Substrate class: Steroids
Product class: Other

Literature & public identifiers

PubMed: PMID:33133120 ↗
DOI: 10.3389/fpls.2020.583622 ↗
UniProt: A0A8F0K7B3 ↗
GenBank: —
NCBI TaxID: —

Regulation of Brassinosteroid Homeostasis in Higher Plants.