Article
The role of the Val353 residue in antagonist binding to rat CCK-B receptors.
Neuroreport - 19 Jun 1995
Malatynska E, Knapp R J, Stropova D, Varga E, Yamamura H I
Abstract excerpt
The Val353 residue of the rat cholecystokinin-B (CCK-B) receptor was mutated to Leu to test whether this residue is part of a binding site for antagonists having different chemical structures. The agonist radioligand [3H]SNF 8702 showed similar affinity for both wild-type and mutant receptors. Mutation of the CCK-B receptor reversed the order of affinities for the asperlicin derivatives from L-365,260 >...
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