Perturbation of the pore of the cystic fibrosis transmembrane conductance regulator (CFTR) inhibits its atpase activity (Q31743298)

3 July 2017

Perturbation of the pore of the cystic fibrosis transmembrane conductance regulator (CFTR) inhibits its atpase activity (English)

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3 July 2017

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transmembrane protein

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author name string

Kogan I

1

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3 July 2017

Ramjeesingh M

2

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3 July 2017

Huan LJ

3

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3 July 2017

Wang Y

4

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3 July 2017

Bear CE

5

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3 July 2017

language of work or name

English

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publication date

21 December 2000

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Journal of Biological Chemistry

3 July 2017

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3 July 2017

276

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3 July 2017

15

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3 July 2017

11575-11581

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Nucleoside triphosphates are required to open the CFTR chloride channel.

3 July 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Amplification of P-glycoprotein genes in multidrug-resistant mammalian cell lines

21 January 2018

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Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

The ABC of channel regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Regulation of CFTR Cl- channel gating by ATP binding and hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Gating of cystic fibrosis transmembrane conductance regulator chloride channels by adenosine triphosphate hydrolysis. Quantitative analysis of a cyclic gating scheme

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

ATPase activity of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Walker mutations reveal loose relationship between catalytic and channel-gating activities of purified CFTR (cystic fibrosis transmembrane conductance regulator)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

A novel procedure for the efficient purification of the cystic fibrosis transmembrane conductance regulator (CFTR)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Relation between the turnover number for vinblastine transport and for vinblastine-stimulated ATP hydrolysis by human P-glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Mutations in the nucleotide-binding sites of P-glycoprotein that affect substrate specificity modulate substrate-induced adenosine triphosphatase activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Cystic fibrosis-associated mutations at arginine 347 alter the pore architecture of CFTR. Evidence for disruption of a salt bridge.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Purification and reconstitution of epithelial chloride channel cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Nonequilibrium gating and voltage dependence of the ClC-0 Cl- channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Gating of the voltage-dependent chloride channel CIC-0 by the permeant anion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Chloride dependence of hyperpolarization-activated chloride channel gates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Cl(-)-channel blockers in the thick ascending limb of the loop of Henle. Structure activity relationship

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Redox reagents and divalent cations alter the kinetics of cystic fibrosis transmembrane conductance regulator channel gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

De novo synthesis of glutathione is required for both entry into and progression through the cell cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Effects of buthionine sulfoximine on the development of ozone-induced pulmonary fibrosis

21 January 2018

1 reference

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Transforming growth factor-beta1 is a potent inhibitor of glutathione synthesis in the lung epithelial cell line A549: transcriptional effect on the GSH rate-limiting enzyme gamma-glutamylcysteine synthetase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Adenosine triphosphate-dependent asymmetry of anion permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Identification of Residues in the Drug-binding Site of Human P-glycoprotein Using a Thiol-reactive Substrate

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Identification of Residues in the Drug-binding Domain of Human P-glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Identification of Residues within the Drug-binding Domain of the Human Multidrug Resistance P-glycoprotein by Cysteine-scanning Mutagenesis and Reaction with Dibromobimane

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

Multi-ion pore behaviour in the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M010403200

21 January 2018

Identifiers

DOI

10.1074/JBC.M010403200

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3 July 2017

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