Novel residues lining the CFTR chloride channel pore identified by functional modification of introduced cysteines (Q46043174)

19 December 2017

title

Novel residues lining the CFTR chloride channel pore identified by functional modification of introduced cysteines (English)

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19 December 2017

2

Paul Linsdell

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19 December 2017

Mohammad Fatehi

1

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19 December 2017

publication date

19 April 2009

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19 December 2017

number of pages

14

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Journal of Membrane Biology

inferred from page(s)

published in

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19 December 2017

volume

228

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19 December 2017

issue

3

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19 December 2017

page(s)

151-164

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19 December 2017

https://scigraph.springernature.com/pub.10.1007/s00232-009-9167-3

exact match

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cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00232-009-9167-3

Phenylalanine-508 mediates a cytoplasmic-membrane domain contact in the CFTR 3D structure crucial to assembly and channel function

21 January 2018

1 reference

12 December 2020

Amino acid residues lining the chloride channel of the cystic fibrosis transmembrane conductance regulator.

1 reference

12 December 2020

Atomic model of human cystic fibrosis transmembrane conductance regulator: membrane-spanning domains and coupling interfaces

1 reference

12 December 2020

Molecular determinants of Au(CN)(2)(-) binding and permeability within the cystic fibrosis transmembrane conductance regulator Cl(-) channel pore

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of a region of strong discrimination in the pore of CFTR.

1 reference

12 December 2020

Substituted-cysteine accessibility method

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12 December 2020

Permeation through the CFTR chloride channel

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12 December 2020

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

1 reference

12 December 2020

Direct comparison of the functional roles played by different transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

12 December 2020

Thiocyanate as a probe of the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of a second blocker binding site at the cytoplasmic mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore.

1 reference

12 December 2020

Characterization of mutations located in exon 18 of the CFTR gene.

1 reference

12 December 2020

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Structure of a bacterial multidrug ABC transporter

1 reference

12 December 2020

Identification of positive charges situated at the outer mouth of the CFTR chloride channel pore

1 reference

12 December 2020

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

1 reference

12 December 2020

On the origin of asymmetric interactions between permeant anions and the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

12 December 2020

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

1 reference

12 December 2020

The ABC protein turned chloride channel whose failure causes cystic fibrosis

1 reference

12 December 2020

Multiple inhibitory effects of Au(CN)(2-) ions on cystic fibrosis transmembrane conductance regulator Cl(-) channel currents

1 reference

12 December 2020

Asymmetric structure of the cystic fibrosis transmembrane conductance regulator chloride channel pore suggested by mutagenesis of the twelfth transmembrane region

1 reference

12 December 2020

Conformational changes in a pore-lining helix coupled to cystic fibrosis transmembrane conductance regulator channel gating

1 reference

12 December 2020

Relationship between anion binding and anion permeability revealed by mutagenesis within the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

12 December 2020

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

1 reference

12 December 2020

Non-pore lining amino acid side chains influence anion selectivity of the human CFTR Cl- channel expressed in mammalian cell lines

1 reference

12 December 2020

Molecular determinants of anion selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

12 December 2020

Structure and function of ABC transporters

1 reference

12 December 2020

Heterologous expression systems for study of cystic fibrosis transmembrane conductance regulator.

1 reference

12 December 2020

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

1 reference

12 December 2020

Interaction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator

1 reference

12 December 2020

Channel-lining residues in the M3 membrane-spanning segment of the cystic fibrosis transmembrane conductance regulator.

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00232-009-9167-3

Identifiers

DOI

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19 December 2017

PubMed ID

19381710

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19 December 2017