Functional arrangement of the 12th transmembrane region in the CFTR chloride channel pore based on functional investigation of a cysteine-less CFTR variant. (Q51766349)

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scientific article published on 28 July 2011

Language	Label	Description	Also known as
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

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1

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Europe PubMed Central

11 April 2018

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

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object named as

Paul Linsdell

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Europe PubMed Central

11 April 2018

author name string

Yassine El Hiani

2

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Europe PubMed Central

11 April 2018

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

publication date

28 July 2011

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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

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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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