Mutations That Change the Position of the Putative γ-Phosphate Linker in the Nucleotide Binding Domains of CFTR Alter Channel Gating

This publication has 43 references indexed in Scilit:

• Differential Interactions of Nucleotides at the Two Nucleotide Binding Domains of the Cystic Fibrosis Transmembrane Conductance Regulator
  Published by Elsevier ,2001
• Walker A Lysine Mutations of TAP1 and TAP2 Interfere with Peptide Translocation but Not Peptide Binding
  Journal of Biological Chemistry, 2001
• The non‐hydrolytic pathway of cystic fibrosis transmembrane conductance regulator ion channel gating
  The Journal of Physiology, 2000
• Structural Biology of Rad50 ATPase
  Cell, 2000
• Gating of Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channels by Adenosine Triphosphate Hydrolysis
  The Journal of general physiology, 1999
• Walker Mutations Reveal Loose Relationship between Catalytic and Channel-Gating Activities of Purified CFTR (Cystic Fibrosis Transmembrane Conductance Regulator)
  Biochemistry, 1999
• Conformational states of CFTR associated with channel gating: The role of ATP binding and hydrolysis
  Cell, 1995
• Regulation of CFTR Cl- channel gating by ADP and ATP analogues.
  The Journal of general physiology, 1995
• Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutation
  Human Molecular Genetics, 1992
• Bacterial periplasmic permeases belong to a family of transport proteins operating from Escherichia coli to human: Traffic ATPases
  FEMS Microbiology Letters, 1990