Control of CFTR channel gating by phosphorylation and nucleotide hydrolysis. (Q53938455)

22 May 2018

review article

1 reference

title

Control of CFTR channel gating by phosphorylation and nucleotide hydrolysis. (English)

1 reference

22 May 2018

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2

1 reference

22 May 2018

author name string

D C Gadsby

series ordinal

1

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22 May 2018

publication date

1 January 1999

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22 May 2018

published in

Physiological Reviews

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22 May 2018

volume

79

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22 May 2018

page(s)

S77-S107

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22 May 2018

issue

1 Suppl

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22 May 2018

Regulation of CFTR ion channel gating by MgATP.

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Genistein activates CFTR Cl- channels via a tyrosine kinase- and protein phosphatase-independent mechanism

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Isotype-specific activation of cystic fibrosis transmembrane conductance regulator-chloride channels by cGMP-dependent protein kinase II.

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Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model

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CFTR and outward rectifying chloride channels are distinct proteins with a regulatory relationship

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The CFTR chloride channel of mammalian heart

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A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins

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Genistein potentiates wild-type and delta F508-CFTR channel activity

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Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

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Alternate stimulation of apical CFTR by genistein in epithelia

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cAMP-independent activation of CFTR Cl channels by the tyrosine kinase inhibitor genistein

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Phosphorylation by protein kinase C is required for acute activation of cystic fibrosis transmembrane conductance regulator by protein kinase A.

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ATPase activity of the cystic fibrosis transmembrane conductance regulator

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Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics

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Identification and partial characterization of a domain in CFTR that may bind cyclic nucleotides directly.

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Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene

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Glibenclamide, an ATP-sensitive K+ channel blocker, inhibits cardiac cAMP-activated Cl- conductance

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Identification of protein kinase A phosphorylation sites on NBD1 and R domains of CFTR using electrospray mass spectrometry with selective phosphate ion monitoring

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A multivalent PDZ-domain protein assembles signalling complexes in a G-protein-coupled cascade.

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ATP alters current fluctuations of cystic fibrosis transmembrane conductance regulator: evidence for a three-state activation mechanism

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Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

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Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

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CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated state

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Human epithelial cystic fibrosis transmembrane conductance regulator without exon 5 maintains partial chloride channel function in intracellular membranes

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1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Modulation of CFTR chloride channels by calyculin A and genistein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Chloride conductance regulated by cyclic AMP-dependent protein kinase in cardiac myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Regulation of CFTR channel gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Regulation of chloride channels by protein kinase C in normal and cystic fibrosis airway epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

The protein kinase A-regulated cardiac Cl- channel resembles the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Phosphorylation fails to activate chloride channels from cystic fibrosis airway cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Multi-ion pore behaviour in the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

Indictment of pore behaviour

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.1999.79.1.S77

10.1152/PHYSREV.1999.79.1.S77

21 January 2018

Identifiers

DOI

1 reference

22 May 2018

PubMed ID

9922377

1 reference

22 May 2018