UGT73C5 (At2g36800, DOGT1, ZOG3; Q9ZQ94) notes

2026-10-21 — Full re-review, independent of the ProtNLM2 predictions

Context: UGT73C5 is reviewed as the experimentally characterised reference for the
UGT73C cluster of PTHR48047 (it seeds PAINT node PTN008730368). No ProtNLM2 output was
consulted.

Deep research

just deep-research-falcon ARATH UGT73C5 --fallback perplexity-lite failed: falcon
raised Exception: Failed to authenticate (Edison client JWT), and the perplexity-lite
fallback returned HTTP 401 insufficient_quota. No deep-research file exists. The
review is built from the cached primary literature (all six GOA PMIDs cached; only
PMID:16214889 has full text) and the curated UniProt record.

Evolutionary placement

Implication for transfer: only UDP-glucosyltransferase activity is phylogenetically
grounded for UGT73C-cluster relatives in other subfamilies (e.g. SF229). The
brassinosteroid 23-O-, DON 3-O-, zeatin O- and quercetin glucosylations are
experimentally established for UGT73C5 itself (Arabidopsis) and must not be
transferred as such.

Experimentally established in Arabidopsis (this protein)

  1. DON detoxification: identified in a yeast cDNA-library screen; transfers glucose from
    UDP-glucose to the C-3 hydroxyl of deoxynivalenol; the glucoside is inactive in a
    wheat-germ translation assay; also detoxifies 15-ADON but not nivalenol; overexpression
    enhances DON tolerance; gene induced by DON, SA, ethylene, JA
    [PMID:12970342, abstract only].
  2. Brassinosteroid 23-O-glucosylation: BL and CS are glucosylated only at the 23-OH (in
    planta feeding, yeast expression); overexpression gives BR-deficient dwarfism rescued
    by epiBL, reduced typhasterol/6-deoxoCS/CS; RNAi silencing abolishes detectable
    BL-23-O-glucoside in seedlings; RNAi lines have slightly longer hypocotyls in low
    fluence red/blue light [PMID:16214889, full text]. The authors note "the data do not
    provide conclusive evidence" that glucosylation is the cause of inactivation.
  3. Cytokinin O-glucosylation in vitro: one of three UGTs (with UGT85A1, UGT73C1) forming
    O-glucosides of trans-zeatin and dihydrozeatin in a 105-UGT screen [PMID:15342621,
    abstract only]; UniProt curated adds in vitro activity on cis-zeatin,
    dihydrozeatin-9-N-Glc and olomoucine, and "not induced by cytokinin treatment".
  4. Quercetin: low 7-O and 4'-O glucosylation in vitro in a 91-UGT screen
    [PMID:15352060, abstract only; specifics from UniProt curated FUNCTION].

Localization

No targeted localisation study. HDA ER call comes from microsomal proteome profiling
(PMID:28887381; gene only in supplementary tables). UniProt "Membrane; single-pass"
is ECO:0000305 inference from a predicted helix (146-162, ECO:0000255); family 1 UGTs
have a soluble GT-B fold, so a true TM span is doubtful. AtSubP chloroplast prediction
(ISM) has no supporting transit-peptide feature; removed.

Decisions summary