| Literature DB >> 24955489 |
William J Belfield1, Daniel J Cole2, Ian L Martin3, Mike C Payne1, P-L Chau4.
Abstract
Constrained geometric simulations have been performed for the recently published closed-channel state of the nicotinic acetylcholine receptor. These simulations support the theory that correlated motion in the flexible β-sheet structure of the extracellular domain helps to communicate a "conformational wave", spreading from the acetylcholine binding pocket. Furthermore, we have identified key residues that act at the interface between subunits and between domains that could potentially facilitate rapid communication between the binding site and the transmembrane gate.Entities:
Keywords: Cys-loop receptors; Ligand-gated ion channels; Membrane protein; Nicotinic acetylcholine receptor; first; froda
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Year: 2014 PMID: 24955489 DOI: 10.1016/j.jmgm.2014.05.001
Source DB: PubMed Journal: J Mol Graph Model ISSN: 1093-3263 Impact factor: 2.518