Search Results
Overview
| Uniprot ID | P54855 |
|---|---|
| Protein Name | UDP-glucuronosyltransferase 2B15 |
| Gene Name | UGT2B15 |
| Organism | Homo sapiens |
Kla Sites from experimental identification
| Position | Flanking peptide |
|---|---|
| 129 | DYSNKLCKDAVLNKK |
| 135 | CKDAVLNKKLMMKLQ |
| 232 | FQIYDLKKWDQFYSE |
| 284 | FVGGLHCKPAKPLPK |
| 287 | GLHCKPAKPLPKEME |
| 344 | LWRFDGKKPNTLGSN |
| 368 | NDLLGHPKTKAFITH |
| 410 | NIAHMKAKGAALSVD |
| 431 | RDLLNALKSVINDPV |
| 440 | VINDPVYKENVMKLS |
| 445 | VYKENVMKLSRIHHD |
| 456 | IHHDQPMKPLDRAVF |
Function
UDP-glucuronosyltransferase (UGT) that catalyzes phase II biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase the metabolite's water solubility, thereby facilitating excretion into either the urine or bile (PubMed:16595710, PubMed:18719240, PubMed:23288867, PubMed:7835232, PubMed:9295060). Essential for the elimination and detoxification of drugs, xenobiotics and endogenous compounds (PubMed:7835232). Catalyzes the glucuronidation of endogenous steroid hormones such as androgens (testosterone, androsterone) and estrogens (estradiol, epiestradiol, estriol, catechol estrogens) (PubMed:16595710, PubMed:18719240, PubMed:23288867, PubMed:7835232, PubMed:9295060). Displays glucuronidation activity toward several classes of xenobiotic substrates, including phenolic compounds (eugenol, 4-nitrophenol, 4-hydroxybiphenyl) and phenylpropanoids (naringenin, coumarins) (PubMed:7835232). Catalyzes the glucuronidation of monoterpenoid alcohols such as borneol, menthol and isomenthol, a class of natural compounds used in essential oils (By similarity)
Protein Sequence
Gene Ontology
| Classification | GO ID | Description |
|---|---|---|
| Cellular Component | GO:0005789 | endoplasmic reticulum membrane |
| Molecular Function | GO:0015020 | glucuronosyltransferase activity |
| Biological Process | GO:0008210 | estrogen metabolic process |
| Biological Process | GO:0008202 | steroid metabolic process |
| Biological Process | GO:0006805 | xenobiotic metabolic process |
Reference
[1] Yang Z, Yan C, Ma J, Peng P, Ren X et al.. Lactylome analysis suggests lactylation-dependent mechanisms of metabolic adaptation in hepatocellular carcinoma.. Nat Metab 5(1):61-79. 2023 Jan. PMID: 36593272.
[2] Hong H, Chen X, Wang H, Gu X, Yuan Y et al.. Global profiling of protein lysine lactylation and potential target modified protein analysis in hepatocellular carcinoma.. Proteomics 23(9):e2200432. 2023 May. PMID: 36625413.