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Unless otherwise stated all data on this page refer to the human proteins. Gene information is provided for human (Hs), mouse (Mm) and rat (Rn).
ASC transporters mediate Na+-dependent exchange of small neutral amino acids such as Ala, Ser, Cys and Thr and their structure is predicted to be similar to that of the glutamate transporters [2,10]. ASCT1 and ASCT2 also exhibit thermodynamically uncoupled chloride channel activity associated with substrate transport [1,4,11]. Whereas EAATs counter-transport K+ (see above) ASCTs do not and their function is independent of the intracellular concentration of K+ [1,11].
ASCT1 (Alanine/serine/cysteine transporter 1 / SLC1A4) C Show summary » |
ASCT2 (Alanine/serine/cysteine transporter 2 / SLC1A5)
C
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Database page citation (select format):
Concise Guide to PHARMACOLOGY citation:
Alexander SP, Kelly E, Mathie A, Peters JA, Veale EL et al. (2021) THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Transporters. Br J Pharmacol. 178 Suppl 1:S412-S513.
The substrate specificity of ASCT1 may extend to L-proline and trans-4-hydroxy-proline [8]. At low pH (~5.5) both ASCT1 and ASCT2 are able to exchange acidic amino acids such as L-cysteate and glutamate [9-10]. In addition to the inhibitors tabulated above, HgCl2, methylmercury and mersalyl, at low micromolar concentrations, non-competitively inhibit ASCT2 by covalent modificiation of cysteine residues [7].