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

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Journal of Physiological Sciences

• Publication date

  2011-04-03

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1007/s12576-011-0144-0PMID 21461971PMCID PMC10717511
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2008influential reference
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  2008cited by this paper
• Monomeric CFTR in Plasma Membranes in Live Cells Revealed by Single Molecule Fluorescence Imaging*

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  2007cited by this paper
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  2007cited by this paper
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  2007influential reference
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  2006cited by this paper
• Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

  2006cited by this paper
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  2006cited by this paper
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  2005cited by this paper
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• Location of a Common Inhibitor Binding Site in the Cytoplasmic Vestibule of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore*

  2005cited by this paper
• Assembly of functional CFTR chloride channels.

  2005cited by this paper
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• On the Mechanism of MgATP-dependent Gating of CFTR Cl− Channels

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  2001cited by this paper
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  2000cited by this paper
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  2000cited by this paper
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  2000cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1998cited by this paper
• Non‐pore lining amino acid side chains influence anion selectivity of the human CFTR Cl− channel expressed in mammalian cell lines

  1998cited by this paper
• Adenosine Triphosphate–dependent Asymmetry of Anion Permeation in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel

  1998influential reference
• Block by MOPS reveals a conformation change in the CFTR pore produced by ATP hydrolysis.

  1997cited by this paper
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  1997influential reference
• Mechanism of Glibenclamide Inhibition of Cystic Fibrosis Transmembrane Conductance Regulator Cl− Channels Expressed in a Murine Cell Line

  1997influential reference
• Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel.

  1996cited by this paper
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  1996cited by this paper
• Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl‐ channels expressed in a mammalian cell line and its regulation by a critical pore residue.

  1996influential reference
• Pyrophosphate Stimulates Wild-type and Mutant Cystic Fibrosis Transmembrane Conductance Regulator Cl− Channels (*)

  1995cited by this paper
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  1995influential reference
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  1995cited by this paper
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  1994cited by this paper
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