(Q31743298)

3 July 2017

title

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

published in

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3 July 2017

volume

276

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3 July 2017

issue

15

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3 July 2017

page(s)

11575-11581

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Nucleoside triphosphates are required to open the CFTR chloride channel.

3 July 2017

cites work

1 reference

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21 January 2018

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21 January 2018

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

21 January 2018

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Generation of cAMP-Activated Chloride Currents by Expression of CFTR

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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ATPase activity of the cystic fibrosis transmembrane conductance regulator

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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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

1 reference

3 July 2017

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