Stoichiometry and novel gating mechanism within the cystic fibrosis transmembrane conductance regulator channel
Author:
Affiliation:
1. Department of Medical Function; School of Medicine; Yangtze University; Jingzhou Hubei Province 434023 China
2. Department of Biology; College of Chemistry and Life Sciences; Zhejiang Normal University; Jinhua Zhejiang Province 321004 China
Publisher
Wiley
Subject
Physiology,Physiology (medical),Nutrition and Dietetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1113/expphysiol.2014.081034/fullpdf
Reference52 articles.
1. Stereochemical preferences modulate affinity and selectivity among five PDZ domains that bind CFTR: comparative structural and sequence analyses;Amacher;Structure,2014
2. Determination of epithelial Na+ channel subunit stoichiometry from single-channel conductances;Anantharam;J Gen Physiol,2007
3. Dual roles of the sixth transmembrane segment of the CFTR chloride channel in gating and permeation;Bai;J Gen Physiol,2010
4. Structural basis for the channel function of a degraded ABC transporter, CFTR (ABCC7);Bai;J Gen Physiol,2011
5. CFTR is a monomer: biochemical and functional evidence;Chen;J Membr Biol,2002
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2. The Pore Architecture of the Cystic Fibrosis Transmembrane Conductance Regulator Channel Revealed by Co-Mutation in Pore-Forming Transmembrane Regions;Physiological Research;2016-06-14
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