Title : Substrate exchange properties of the high-affinity glutamate transporter EAAT2.

Pub. Date : 2001 Nov 1

PMID : 11746366






1 Functional Relationships(s)
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1 L-Aspartate, L-glutamate and L-cysteate produced an equivalent degree of [3H] exchange to that observed with D-aspartate, although the non-substrate EAAT2 inhibitor dihydrokainate and D-glutamate, which does not interact with the substrate binding site, failed to stimulate [3H]D-aspartate exchange. L-Cysteic acid solute carrier family 1 member 2 Homo sapiens