Target intelligence / Profile preview

UDP-glycosyltransferase 3A1 (UGT3A1)

Target
UGT3A1
Molecular classification
Enzyme, Glycosyltransferase, Phase II metabolic enzyme, Transferase
01

Overview

UDP-glycosyltransferase 3A1 (UGT3A1) is an enzyme of the glycosyltransferase superfamily, functioning primarily as a phase II metabolic enzyme that catalyzes the transfer of glycosyl groups from nucleotide sugars (such as UDP-glucose or UDP-N-acetylglucosamine) to small molecule substrates. This enzymatic activity is part of the body's detoxification system, aiding in the conjugation and elimination of various endogenous and exogenous substances through glucosidation and glycosylation. Unlike the more common UGT1A and UGT2B families associated with glucuronidation, UGT3A1 uses glucose and N-acetylglucosamine as donor molecules rather than glucuronic acid. UGT3A1 is expressed in human tissues such as the liver and kidney and may influence the metabolism of certain drugs, steroids, and xenobiotics. Dysregulation or genetic variants in UGT3A1 can affect drug response and toxicity, though it is not currently a primary therapeutic target. Its function in drug metabolism and disposition, along with potential links to disease and variability in drug handling, make it of clinical and pharmacogenetic interest[3].

Other names
UDP-glucuronosyltransferase 3A1UDPGT 3A1FLJ34658UDP glycosyltransferase 3 family, polypeptide A1
02

Mechanism of action

Glucosidation of xenobiotics and other small molecules, sometimes increasing solubility and enhancing excretion

03

Biological functions

Conjugation of xenobiotics and endogenous substratesGlucosidation and glycosylation reactionsDetoxificationMetabolic processing of small molecules
04

Disease associations

CancerDrug metabolism-related toxicityOther
05

Safety considerations

Potential for variability in drug metabolism leading to altered drug exposure or toxicity.Genetic polymorphisms could cause interindividual differences in drug response.
06

Interacting drugs

No FDA-approved drugs selectively target UGT3A1 as a primary molecular target, but various drugs and chemicals can be substrates for UGT3A1-catalyzed reactions
07

Biomarkers

No established biomarkers for patient selection or efficacy specifically for UGT3A1

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