ATP hydrolysis-dependent asymmetry of the conformation of CFTR channel pore

A stable ATP binding to the nucleotide binding domain is important for reliable gating cycle in an ABC transporter CFTR

(2010) Hiroyasu Shimizu et al.   Journal of Physiological Sciences

CFTR Functions as a Bicarbonate Channel in Pancreatic Duct Cells

(2009) Hiroshi Ishiguro et al.   JOURNAL OF GENERAL PHYSIOLOGY

The maxi-anion channel: a classical channel playing novel roles through an unidentified molecular entity

(2009) Ravshan Z. Sabirov et al.   Journal of Physiological Sciences

Relationship between nucleotide binding and ion channel gating in cystic fibrosis transmembrane conductance regulator

(2009) Andrei A. Aleksandrov et al.   JOURNAL OF PHYSIOLOGY-LONDON

Architecture of the cystic fibrosis transmembrane conductance regulator protein and structural changes associated with phosphorylation and nucleotide binding

(2009) Liang Zhang et al.   JOURNAL OF STRUCTURAL BIOLOGY

Atomic model of human cystic fibrosis transmembrane conductance regulator: Membrane-spanning domains and coupling interfaces

(2008) J.-P. Mornon et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Monomeric CFTR in Plasma Membranes in Live Cells Revealed by Single Molecule Fluorescence Imaging

(2008) Peter M. Haggie et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Three-dimensional Reconstruction of Human Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Revealed an Ellipsoidal Structure with Orifices beneath the Putative Transmembrane Domain

(2008) Kazuhiro Mio et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mechanism of direct bicarbonate transport by the CFTR anion channel

(2008) Lin Tang et al.   Journal of Cystic Fibrosis

Mutations at Arginine 352 Alter the Pore Architecture of CFTR

(2008) Guiying Cui et al.   JOURNAL OF MEMBRANE BIOLOGY

ATP hydrolysis-driven gating in cystic fibrosis transmembrane conductance regulator

(2008) D. Muallem et al.   PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES

Evolutionary and functional divergence between the cystic fibrosis transmembrane conductance regulator and related ATP-binding cassette transporters

(2008) I. King Jordan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Phenylalanine-508 mediates a cytoplasmic-membrane domain contact in the CFTR 3D structure crucial to assembly and channel function

(2008) A. W. R. Serohijos et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA