Target intelligence / Profile preview

Multidrug and toxin extrusion protein 2 (MATE2)

Target
MATE2
Molecular classification
Transporter, Solute carrier family (SLC47 family), Multidrug and toxin extrusion transporter
01

Overview

Multidrug and toxin extrusion protein 2 (MATE2), encoded by the SLC47A2 gene, is a membrane transporter primarily expressed in the kidney, where it mediates the excretion of endogenous and exogenous organic cations, including many drugs, into urine through a proton-coupled antiport mechanism. MATE2 is a member of the MATE transporter family (part of the SLC47 solute carrier family), sharing homology with bacterial MATE proteins and characterized structurally by 12 transmembrane helices. MATE2 works collaboratively with other transporters (such as OCT2) to facilitate renal and hepatic clearance of cationic compounds, and its function is crucial for determining the pharmacokinetics of several commonly used medications. Genetic polymorphisms in MATE2 can influence transporter expression and activity, affecting patient response and the risk of adverse drug effects for substrates such as metformin and cimetidine. MATE2 is thus an important target for understanding drug-drug interactions, adverse drug responses, and personalized medicine involving transporter-mediated drug clearance.

Other names
SLC47A2MATE2MATE2-B
02

Mechanism of action

Inhibition of organic cation transport, Modulation of renal and hepatic clearance, Proton-coupled antiport, Drug-drug interaction via transporter inhibition

03

Biological functions

Excretion of organic cationsRenal and hepatic drug clearanceDetoxificationXenobiotic transportOrganic cation/proton antiport
04

Disease associations

Drug disposition variabilityDrug resistanceAdverse drug reactionsOther
05

Safety considerations

Genetic variability leading to altered drug handling and risk for toxicityinhibition can cause changes in drug levels (notably metformin)
06

Interacting drugs

Metformin

9 more in the full profile.

07

Biomarkers

Polymorphisms in SLC47A2 affecting drug pharmacokinetics/metformin response

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