(Q51766349)

English

Functional arrangement of the 12th transmembrane region in the CFTR chloride channel pore based on functional investigation of a cysteine-less CFTR variant.

scientific article published on 28 July 2011

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scholarly article

1 reference

Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

Functional arrangement of the 12th transmembrane region in the CFTR chloride channel pore based on functional investigation of a cysteine-less CFTR variant. (English)

1 reference

Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

transmembrane protein

0 references

1

1 reference

Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

3

object named as

Paul Linsdell

1 reference

Europe PubMed Central

11 April 2018

author name string

Yassine El Hiani

2

1 reference

Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

publication date

28 July 2011

1 reference

Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

Pfluegers Archiv

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Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

462

1 reference

Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

4

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Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

559-571

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Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

https://scigraph.springernature.com/pub.10.1007/s00424-011-0998-2

0 references

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Cystic fibrosis transmembrane conductance regulator: using differential reactivity toward channel-permeant and channel-impermeant thiol-reactive probes to test a molecular model for the pore

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Dual roles of the sixth transmembrane segment of the CFTR chloride channel in gating and permeation

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

The DeltaF508 mutation disrupts packing of the transmembrane segments of the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

The role of cystic fibrosis transmembrane conductance regulator phenylalanine 508 side chain in ion channel gating

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Changes in accessibility of cytoplasmic substances to the pore associated with activation of the cystic fibrosis transmembrane conductance regulator chloride channel

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

The ABC protein turned chloride channel whose failure causes cystic fibrosis

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Point mutations in the pore region directly or indirectly affect glibenclamide block of the CFTR chloride channel

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

The ATP-binding cassette family: a structural perspective.

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Cysteine-independent inhibition of the CFTR chloride channel by the cysteine-reactive reagent sodium (2-sulphonatoethyl) methanethiosulphonate

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Review. Structure and mechanism of ATP-binding cassette transporters

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

In vivo phosphorylation of CFTR promotes formation of a nucleotide-binding domain heterodimer

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Three-dimensional reconstruction of human cystic fibrosis transmembrane conductance regulator chloride channel revealed an ellipsoidal structure with orifices beneath the putative transmembrane domain

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Molecular models of the open and closed states of the whole human CFTR protein

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

ABC transporters: the power to change

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Architecture of the cystic fibrosis transmembrane conductance regulator protein and structural changes associated with phosphorylation and nucleotide binding.

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Direct comparison of NPPB and DPC as probes of CFTR expressed in Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

Regulation of conductance by the number of fixed positive charges in the intracellular vestibule of the CFTR chloride channel pore

1 reference

https://api.crossref.org/works/10.1007%2FS00424-011-0998-2

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21796338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alignment of transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

https://pubmed.ncbi.nlm.nih.gov/21796338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21796338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Permeation through the CFTR chloride channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/21796338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21796338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of proline residues in the membrane-spanning domains of cystic fibrosis transmembrane conductance regulator to chloride channel function

1 reference

https://pubmed.ncbi.nlm.nih.gov/21796338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00424-011-0998-2

1 reference

Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

1 reference

Europe PubMed Central

11 April 2018

http://europepmc.org/abstract/MED/21796338

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