Article
The binding of propranolol at 5-hydroxytryptamine1D beta T355N mutant receptors may involve formation of two hydrogen bonds to asparagine.
Molecular pharmacology - 1 Jan 1996
Glennon R A, Dukat M, Westkaemper R B, Ismaiel A M, Izzarelli D G, Parker E M
Abstract excerpt
Although the beta-adrenergic receptor antagonist (-)-propranolol binds with relatively low affinity at human 5-hydroxytryptamine1D beta receptors (Ki = 10,200 nM), it displays significantly higher affinity (Ki = 17 nM) at its species homolog, 5-HT1B receptors, and at a mutant 5-HT1D beta receptor (Ki = 16 nM), where the threonine residue at position 355 (T355) is replaced with an asparagine residue (i.e., a T355N...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
