(Q40500058)

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

21 September 2017

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

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Europe PubMed Central

PubMed publication ID

21 September 2017

cystic fibrosis

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transmembrane protein

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4

object named as

Paul Linsdell

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Europe PubMed Central

PubMed publication ID

21 September 2017

author name string

Ning Ge

1

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Europe PubMed Central

PubMed publication ID

21 September 2017

Chantal N Muise

2

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Europe PubMed Central

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21 September 2017

Xiandi Gong

3

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Europe PubMed Central

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21 September 2017

language of work or name

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publication date

25 October 2004

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21 September 2017

Journal of Biological Chemistry

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21 September 2017

279

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Europe PubMed Central

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21 September 2017

53

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Europe PubMed Central

PubMed publication ID

21 September 2017

55283-55289

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Europe PubMed Central

PubMed publication ID

21 September 2017

The human ATP-binding cassette (ABC) transporter superfamily

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

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/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

The cystic fibrosis transmembrane conductance regulator: an intriguing protein with pleiotropic functions

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https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

Extent of the selectivity filter conferred by the sixth transmembrane region in the CFTR chloride channel pore

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

Cystic fibrosis transmembrane conductance regulator (CFTR) anion binding as a probe of the pore

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

Alternate translation initiation codons can create functional forms of cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

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/10.1074%2FJBC.M411935200

21 January 2018

Structure of MsbA from Vibrio cholera: a multidrug resistance ABC transporter homolog in a closed conformation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

Three-dimensional structures of the mammalian multidrug resistance P-glycoprotein demonstrate major conformational changes in the transmembrane domains upon nucleotide binding

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

Maximization of the rate of chloride conduction in the CFTR channel pore by ion-ion interactions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

Coupled movement of permeant and blocking ions in the CFTR chloride channel pore

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

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/10.1074%2FJBC.M411935200

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/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

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/10.1074%2FJBC.M411935200

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/10.1074%2FJBC.M411935200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

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/10.1074%2FJBC.M411935200

21 January 2018

Molecular modeling correctly predicts the functional importance of Phe594 in transmembrane helix 11 of the multidrug resistance protein, MRP1 (ABCC1).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M411935200

21 January 2018

Identifiers

10.1074/JBC.M411935200

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

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