Cystic fibrosis transmembrane conductance regulator gating requires cytosolic electrolytes (Q31668598)

3 July 2017

Cystic fibrosis transmembrane conductance regulator gating requires cytosolic electrolytes (English)

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3 July 2017

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transmembrane protein

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author name string

Wu JV

1

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3 July 2017

Joo NS

2

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3 July 2017

Krouse ME

3

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3 July 2017

Wine JJ

4

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3 July 2017

language of work or name

English

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publication date

8 December 2000

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Journal of Biological Chemistry

3 July 2017

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3 July 2017

276

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3 July 2017

6473-6478

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3 July 2017

9

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An inventory of the human ABC proteins

3 July 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Nucleoside triphosphates are required to open the CFTR chloride channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Coupling of CFTR Cl- channel gating to an ATP hydrolysis cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Gating of cystic fibrosis transmembrane conductance regulator chloride channels by adenosine triphosphate hydrolysis. Quantitative analysis of a cyclic gating scheme

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Regulation of CFTR Cl- channel gating by ATP binding and hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

ClC and CFTR chloride channel gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Redox reagents and divalent cations alter the kinetics of cystic fibrosis transmembrane conductance regulator channel gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Distinct deactivation and desensitization kinetics of recombinant GABAA receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Disruption of monolayer integrity enables activation of a cystic fibrosis "bypass" channel in human airway epithelia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Activation of volume-regulated chloride currents by reduction of intracellular ionic strength in bovine endothelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Origin of the potassium and voltage dependence of the cardiac inwardly rectifying K-current (IK1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Electrophysiological characterization of the rat epithelial Na+ channel (rENaC) expressed in MDCK cells. Effects of Na+ and Ca2+.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Chloride dependence of hyperpolarization-activated chloride channel gates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Characterization of transport through the periplasmic histidine permease using proteoliposomes reconstituted by dialysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Characterization of the adenosine triphosphatase activity of the periplasmic histidine permease, a traffic ATPase (ABC transporter).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Cystic fibrosis-associated mutations at arginine 347 alter the pore architecture of CFTR. Evidence for disruption of a salt bridge.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

P-glycoprotein-mediated Hoechst 33342 transport out of the lipid bilayer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

An excitatory amino-acid transporter with properties of a ligand-gated chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Ion fluxes associated with excitatory amino acid transport.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

ABC1, an ATP binding cassette transporter required for phagocytosis of apoptotic cells, generates a regulated anion flux after expression in Xenopus laevis oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009305200

21 January 2018

Identifiers

DOI

10.1074/JBC.M009305200

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3 July 2017

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