Cysteine residues in the nucleotide binding domains regulate the conductance state of CFTR channels.

Ítems similars

• Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator
  per: Schwiebert, Erik M., et al.
  Publicat: (1998)
• Gating of the CFTR Cl(−) channel by ATP-driven nucleotide-binding domain dimerisation
  per: Hwang, Tzyh-Chang, et al.
  Publicat: (2009)
• CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated state
  Publicat: (1996)
• CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains
  per: Vergani, Paola, et al.
  Publicat: (2005)
• Normal gating of CFTR requires ATP binding to both nucleotide-binding domains and hydrolysis at the second nucleotide-binding domain
  per: Berger, Allan L., et al.
  Publicat: (2005)