(Q40029008)

16 September 2017

title

State-dependent access of anions to the cystic fibrosis transmembrane conductance regulator chloride channel pore (English)

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16 September 2017

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transmembrane protein

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2

Paul Linsdell

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16 September 2017

Mohammad Fatehi

1

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16 September 2017

language of work or name

English

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publication date

31 December 2007

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Journal of Biological Chemistry

16 September 2017

number of pages

8

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based on heuristic

inferred from page(s)

published in

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16 September 2017

volume

283

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16 September 2017

issue

10

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16 September 2017

page(s)

6102-6109

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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

16 September 2017

cites work

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https://api.crossref.org/works/10.1074%2FJBC.M707736200

Molecular basis for the chloride channel activity of cystic fibrosis transmembrane conductance regulator and the consequences of disease-causing mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Purification and crystallization of the cystic fibrosis transmembrane conductance regulator (CFTR).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

The ABC protein turned chloride channel whose failure causes cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

CFTR (ABCC7) is a hydrolyzable-ligand-gated channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Adenosine triphosphate-dependent asymmetry of anion permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

CFTR: covalent and noncovalent modification suggests a role for fixed charges in anion conduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Positive charges at the intracellular mouth of the pore regulate anion conduction in the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Mutation-induced blocker permeability and multiion block of the CFTR chloride channel pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

CFTR: Ligand exchange between a permeant anion ([Au(CN)2]-) and an engineered cysteine (T338C) blocks the pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Molecular determinants and role of an anion binding site in the external mouth of the CFTR chloride channel pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Location of a common inhibitor binding site in the cytoplasmic vestibule of the cystic fibrosis transmembrane conductance regulator chloride channel pore.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Direct and indirect effects of mutations at the outer mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

State-dependent chemical reactivity of an engineered cysteine reveals conformational changes in the outer vestibule of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

CFTR: a cysteine at position 338 in TM6 senses a positive electrostatic potential in the pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Cystic fibrosis transmembrane conductance regulator. Physical basis for lyotropic anion selectivity patterns

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

Novel pore-lining residues in CFTR that govern permeation and open-channel block

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707736200

21 January 2018

Identifiers

DOI

10.1074/JBC.M707736200

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16 September 2017

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