The role of residues in binding loop A in desflurane and propofol modulation of recombinant 5-HT3A receptor
Author:
Funder
Yonsei University College of Medicine
Publisher
Elsevier BV
Subject
General Neuroscience
Reference24 articles.
1. Molecular actions of propofol on human 5-HT3A receptors: enhancement as well as inhibition by closely related phenol derivatives;Barann;Anesth. Analg.,2008
2. Analysis of the ligand binding site of the 5-HT3 receptor using site directed mutagenesis: importance of glutamate 106;Boess;Neuropharmacology,1997
3. Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors;Brejc;Nature,2001
4. Anaesthetic binding sites for etomidate and propofol on a GABAA receptor model;Campagna-Slater;Neurosci. Lett.,2007
5. A single glycine residue at the entrance to the first membrane-spanning domain of the gamma-aminobutyric acid type A receptor beta(2) subunit affects allosteric sensitivity to GABA and anesthetics;Carlson;Mol. Pharmacol.,2000
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