CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates. (Q41056312)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9463368%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates (English)

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9 November 2019

1

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9 November 2019

J. Kevin Foskett

series ordinal

3

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9 November 2019

author name string

Yue Y

series ordinal

2

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9 November 2019

language of work or name

English

0 references

publication date

1 February 1998

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9 November 2019

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9 November 2019

volume

17

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9 November 2019

page(s)

898-908

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9 November 2019

issue

4

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

9 November 2019

cites work

1 reference

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

26 September 2017

1 reference

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Block by MOPS reveals a conformation change in the CFTR pore produced by ATP hydrolysis.

26 September 2017

1 reference

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Mechanism of glibenclamide inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a murine cell line

26 September 2017

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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

26 September 2017

1 reference

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ATPase activity of the cystic fibrosis transmembrane conductance regulator

26 September 2017

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Cystic fibrosis transmembrane conductance regulator activation stimulates endosome fusion in vivo

26 September 2017

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Autocrine signaling through ATP release represents a novel mechanism for cell volume regulation

26 September 2017

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Glibenclamide blockade of CFTR chloride channels.

26 September 2017

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

26 September 2017

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Voltage-dependent block of the cystic fibrosis transmembrane conductance regulator Cl- channel by two closely related arylaminobenzoates

26 September 2017

1 reference

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Biochemistry of multidrug resistance mediated by the multidrug transporter

26 September 2017

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Protein kinase C-mediated phosphorylation of the human multidrug resistance P-glycoprotein regulates cell volume-activated chloride channels

26 September 2017

1 reference

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Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion

26 September 2017

1 reference

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Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

26 September 2017

1 reference

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CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding

26 September 2017

1 reference

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Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Mutation of lysine-48 to arginine in the yeast RAD3 protein abolishes its ATPase and DNA helicase activities but not the ability to bind ATP.

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Identification of the cystic fibrosis gene: chromosome walking and jumping

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

ABC Transporters: From Microorganisms to Man

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Homodimeric architecture of a ClC-type chloride ion channel

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP.

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

CFTR-independent ATP release from epithelial cells triggered by mechanical stimuli.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Cellular ATP release by the cystic fibrosis transmembrane conductance regulator

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Purified cystic fibrosis transmembrane conductance regulator (CFTR) does not function as an ATP channel

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Nucleotide-induced conformational changes of MalK, a bacterial ATP binding cassette transporter protein.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by negative charge in the R domain.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Interaction of nucleotides with membrane-associated cystic fibrosis transmembrane conductance regulator

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Biochemical and biophysical identification of cystic fibrosis transmembrane conductance regulator chloride channels as components of endocytic clathrin-coated vesicles

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Nucleoside triphosphates are required to open the CFTR chloride channel.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

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

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

A Multifunctional Aqueous Channel Formed by CFTR

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Independent gating of single pores in CLC-0 chloride channels

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Two physically distinct pores in the dimeric ClC-0 chloride channel.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

5'-Adenylylimidodiphosphate does not activate CFTR chloride channels in cell-free patches of membrane

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Effects of pyrophosphate and nucleotide analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator channel gating.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

Coupling of CFTR Cl- channel gating to an ATP hydrolysis cycle.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1170439

CFTR channels expressed in CHO cells do not have detectable ATP conductance

19 August 2018

1 reference

12 December 2020

Flickery block of single CFTR chloride channels by intracellular anions and osmolytes

1 reference

12 December 2020

Multi-ion pore behaviour in the CFTR chloride channel

1 reference

12 December 2020

The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel

1 reference

12 December 2020

Cystic fibrosis transmembrane conductance regulator-associated ATP and adenosine 3'-phosphate 5'-phosphosulfate channels in endoplasmic reticulum and plasma membranes

1 reference

12 December 2020

Apical and basolateral ATP stimulates tracheal epithelial chloride secretion via multiple purinergic receptors

1 reference

12 December 2020

Identifiers

DOI

10.1093/EMBOJ/17.4.898

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9463368%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9463368%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference