(Q42024754)

English

Stable dimeric assembly of the second membrane-spanning domain of CFTR (cystic fibrosis transmembrane conductance regulator) reconstitutes a chloride-selective pore

scientific article published on November 2003

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Stable dimeric assembly of the second membrane-spanning domain of CFTR (cystic fibrosis transmembrane conductance regulator) reconstitutes a chloride-selective pore (English)

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

transmembrane protein

0 references

cystic fibrosis

0 references

author name string

Mohabir Ramjeesingh

1

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Francisca Ugwu

2

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Canhui Li

3

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Sonja Dhani

4

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Ling Jun Huan

5

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Yanchun Wang

6

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Christine E Bear

7

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

language of work or name

0 references

publication date

1 November 2003

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

number of pages

9

1 reference

based on heuristic

inferred from page(s)

Biochemical Journal

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

375

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Pt 3

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

633-641

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

CFTR directly mediates nucleotide-regulated glutathione flux.

1 reference

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X-ray structure of a voltage-dependent K+ channel

1 reference

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The E. coli BtuCD structure: a framework for ABC transporter architecture and mechanism

1 reference

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

1 reference

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5 June 2018

RETRACTED: Structure of MsbA from E. coli: a homolog of the multidrug resistance ATP binding cassette (ABC) transporters

1 reference

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A monomer is the minimum functional unit required for channel and ATPase activity of the cystic fibrosis transmembrane conductance regulator

1 reference

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A novel CFTR disease-associated mutation causes addition of an extra N-linked oligosaccharide

1 reference

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

1 reference

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Direct block of the cystic fibrosis transmembrane conductance regulator Cl(-) channel by butyrate and phenylbutyrate

1 reference

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Characterization of the oligosaccharide structures associated with the cystic fibrosis transmembrane conductance regulator

1 reference

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Severed molecules functionally define the boundaries of the cystic fibrosis transmembrane conductance regulator's NH(2)-terminal nucleotide binding domain

1 reference

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

1 reference

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5 June 2018

Permeation through the CFTR chloride channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1223717

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1223717

5 June 2018

High-level expression, functional reconstitution, and quaternary structure of a prokaryotic ClC-type chloride channel

1 reference

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5 June 2018

Structure and function of the CFTR chloride channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1223717

5 June 2018

The second half of the cystic fibrosis transmembrane conductance regulator forms a functional chloride channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1223717

5 June 2018

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

1 reference

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5 June 2018

Multi-Ion mechanism for ion permeation and block in the cystic fibrosis transmembrane conductance regulator chloride channel

1 reference

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5 June 2018

Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1223717

5 June 2018

Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1223717

5 June 2018

Locating the anion-selectivity filter of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1223717

5 June 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

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Silver-staining of proteins in polyacrylamide gels: a general overview

1 reference

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

1 reference

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5 June 2018

The amino-terminal portion of CFTR forms a regulated Cl- channel.

1 reference

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

1 reference

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Solubilization and functional reconstitution of a chloride channel fromTorpedo californica electroplax

1 reference

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The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation

1 reference

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A simplification of the protein assay method of Lowry et al. which is more generally applicable

1 reference

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Chemical modification of bovine heart mitochondrial malate dehydrogenase. Selective modification of cysteine and histidine

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

1 reference

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Membrane topology of subunit a of the F1F0 ATP synthase as determined by labeling of unique cysteine residues

1 reference

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Arg352 is a major determinant of charge selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel

1 reference

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based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892562

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based on heuristic

inferred from PubMed ID database lookup

Multi-ion pore behaviour in the CFTR chloride channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892562

12 December 2020

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inferred from PubMed ID database lookup

Cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype and phenotype in cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892562

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inferred from PubMed ID database lookup

Covalent modification of the regulatory domain irreversibly stimulates cystic fibrosis transmembrane conductance regulator

1 reference

https://pubmed.ncbi.nlm.nih.gov/12892562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1042/BJ20030774

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

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