Destabilization of the Transmembrane Domain Induces Misfolding in a Phenotypic Mutant of Cystic Fibrosis Transmembrane Conductance Regulator
Open Access
- 1 February 2005
- journal article
- Published by Elsevier
- Vol. 280 (6) , 4968-4974
- https://doi.org/10.1074/jbc.m410069200
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Proline Substitutions are not Easily Accommodated in a Membrane ProteinJournal of Molecular Biology, 2004
- RETRACTED: Structure of MsbA from Vibrio cholera: A Multidrug Resistance ABC Transporter Homolog in a Closed ConformationJournal of Molecular Biology, 2003
- The Role of the C Terminus and Na+/H+ Exchanger Regulatory Factor in the Functional Expression of Cystic Fibrosis Transmembrane Conductance Regulator in Nonpolarized Cells and EpitheliaJournal of Biological Chemistry, 2003
- The influence of proline residues on α‐helical structurePublished by Wiley ,2001
- Relationship between anion binding and anion permeability revealed by mutagenesis within the cystic fibrosis transmembrane conductance regulator chloride channel poreThe Journal of Physiology, 2001
- Guidelines for membrane protein engineering derived from de novo designed model peptidesBiopolymers, 1998
- Management of Pulmonary Disease in Patients with Cystic FibrosisNew England Journal of Medicine, 1996
- Proline residues in transmembrane helixes: structural or dynamic role?Biochemistry, 1991
- Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion SelectivityScience, 1991
- Proline kinks in transmembrane α-helicesJournal of Molecular Biology, 1991