CYP90B1

Choe et CYP90B

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

Substrate

campesterol

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

CYP90B1

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

(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=…

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; CYP90B1 (DWF4) catalyzes C22 hydroxylation of campesterol; in vitro evidence from Choe et al., 1998; Fujita et al., 2006.

Reaction & quality gates

Mechanism: Hydroxylation (+15.99 Da)
Evidence type: In vitro
Confidence: High
Data tier: Gold
Latin binomial + experiment + dual SMILES + ΔMass pass
Substrate class: Steroids
Product class: Steroids

Literature & public identifiers

PubMed: PMID:33133120 ↗
DOI: 10.3389/fpls.2020.583622 ↗
UniProt: A0A8F0FRG5 ↗
GenBank: —
NCBI TaxID: —

Regulation of Brassinosteroid Homeostasis in Higher Plants.