(Q41725516)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9511930%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

review article

1 reference

title

Probing the structural and functional domains of the CFTR chloride channel (English)

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10 November 2019

1

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10 November 2019

author name string

M Cheung

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9511930%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

R Guinamard

series ordinal

3

1 reference

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10 November 2019

language of work or name

1 reference

1 October 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9511930%20AND%20SRC:MED&resulttype=core&format=json

Journal of Bioenergetics and Biomembranes

10 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9511930%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9511930%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

453-463

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9511930%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

5

1 reference

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https://scigraph.springernature.com/pub.10.1023/a:1022482923122

10 November 2019

exact match

0 references

cites work

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Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene

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Molecular determinants of channel function

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

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Structural basis for sugar translocation through maltoporin channels at 3.1 A resolution

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Anion selectivity in biological systems

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Electrostatic potential of the acetylcholine binding sites in the nicotinic receptor probed by reactions of binding-site cysteines with charged methanethiosulfonates

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

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Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by specific protein kinases and protein phosphatases

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

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

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Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

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Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

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

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12 December 2020

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

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Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents

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Structure of the NMDA receptor channel M2 segment inferred from the accessibility of substituted cysteines.

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Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

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

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Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

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

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CFTR displays voltage dependence and two gating modes during stimulation

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

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Regulation of CFTR Cl- channel gating by ADP and ATP analogues

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12 December 2020

Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency.

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12 December 2020

Tolbutamide causes open channel blockade of cystic fibrosis transmembrane conductance regulator Cl- channels

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12 December 2020

Disease-associated mutations in the fourth cytoplasmic loop of cystic fibrosis transmembrane conductance regulator compromise biosynthetic processing and chloride channel activity.

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12 December 2020

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

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12 December 2020

Nucleoside triphosphates are required to open the CFTR chloride channel.

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12 December 2020

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

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12 December 2020

Effect of Deleting the R Domain on CFTR-Generated Chloride Channels

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12 December 2020

Ionic selectivity revisited: The role of kinetic and equilibrium processes in ion permeation through channels

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12 December 2020

Acetylcholine receptor channel structure probed in cysteine-substitution mutants.

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Protein kinase C activates chloride conductance in C127 cells stably expressing the cystic fibrosis gene

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N-glycosylation site tagging suggests a three transmembrane domain topology for the glutamate receptor GluR1.

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Classical electrostatics in biology and chemistry

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The CFTR chloride channel of mammalian heart

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12 December 2020

Molecular Architecture and Electrostatic Properties of a Bacterial Porin

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Identification of acetylcholine receptor channel-lining residues in the entire M2 segment of the alpha subunit.

1 reference

12 December 2020

Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulation

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12 December 2020

Structural and functional similarities between the nucleotide-binding domains of CFTR and GTP-binding proteins

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12 December 2020

CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated state

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12 December 2020

Reactivity of small thiolate anions and cysteine-25 in papain toward methyl methanethiosulfonate

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12 December 2020

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

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12 December 2020

The cystic fibrosis transmembrane conductance regulator. Nucleotide binding to a synthetic peptide segment from the second predicted nucleotide binding fold.

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12 December 2020

The cystic fibrosis transmembrane conductance regulator

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12 December 2020

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

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12 December 2020

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

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12 December 2020

Crystal structures explain functional properties of two E. coli porins

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12 December 2020

ABC Transporters: From Microorganisms to Man

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12 December 2020

Functionally distinct phospho-forms underlie incremental activation of protein kinase-regulated Cl- conductance in mammalian heart

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12 December 2020

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

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12 December 2020

Generation, translocation, and presentation of MHC class I-restricted peptides

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12 December 2020

The first nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator can function as an active ATPase

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12 December 2020

cAMP-dependent protein kinase-mediated phosphorylation of cystic fibrosis transmembrane conductance regulator residue Ser-753 and its role in channel activation

1 reference

12 December 2020

Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulator

1 reference

12 December 2020

Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator.

1 reference

12 December 2020

Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertion.

1 reference

12 December 2020

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

1 reference

12 December 2020

Multi-ion pore behaviour in the CFTR chloride channel

1 reference

12 December 2020

The nature of the accessible and buried surfaces in proteins

1 reference

12 December 2020

Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites

1 reference

12 December 2020

Toxigenic diarrheas, congenital diarrheas, and cystic fibrosis: disorders of intestinal ion transport

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12 December 2020

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

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12 December 2020

Pore loops: an emerging theme in ion channel structure

1 reference

12 December 2020

A Multifunctional Aqueous Channel Formed by CFTR

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12 December 2020

The cystic fibrosis transmembrane conductance regulator. Overexpression, purification, and characterization of wild type and delta F508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein.

1 reference

12 December 2020

Traffic ATPases: a superfamily of transport proteins operating from Escherichia coli to humans

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12 December 2020

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

1 reference

12 December 2020

Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

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12 December 2020

cAMP-stimulated ion currents in Xenopus oocytes expressing CFTR cRNA

1 reference

12 December 2020

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

12 December 2020

Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1022482923122

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9511930%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

10 November 2019

0 references

1 reference