Cystic Fibrosis Transmembrane Conductance Regulator: A Molecular Model Defines the Architecture of the Anion Conduction Path and Locates a “Bottleneck” in the Pore

This publication has 64 references indexed in Scilit:

• The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)
  Journal of Biological Chemistry, 2011
• Cystic Fibrosis Transmembrane Conductance Regulator: Temperature-Dependent Cysteine Reactivity Suggests Different Stable Conformers of the Conduction Pathway
  Biochemistry, 2011
• Tunable pKa values and the basis of opposite charge selectivities in nicotinic-type receptors
  Nature, 2011
• Changes in Accessibility of Cytoplasmic Substances to the Pore Associated with Activation of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel
  Journal of Biological Chemistry, 2010
• Cystic Fibrosis Transmembrane Conductance Regulator: Using Differential Reactivity toward Channel-Permeant and Channel-Impermeant Thiol-Reactive Probes To Test a Molecular Model for the Pore
  Biochemistry, 2009
• Ion channels versus ion pumps: the principal difference, in principle
  Nature Reviews Molecular Cell Biology, 2009
• Phenylalanine-508 mediates a cytoplasmic–membrane domain contact in the CFTR 3D structure crucial to assembly and channel function
  Proceedings of the National Academy of Sciences, 2008
• Mutations at Arginine 352 Alter the Pore Architecture of CFTR
  The Journal of Membrane Biology, 2008
• Flexibility in the ABC transporter MsbA: Alternating access with a twist
  Proceedings of the National Academy of Sciences, 2007
• In vivo phosphorylation of CFTR promotes formation of a nucleotide‐binding domain heterodimer
  The EMBO Journal, 2006