(Q43691957)

25 November 2017

title

A model of reversible inhibitors in the gastric H+/K+-ATPase binding site determined by rotational echo double resonance NMR. (English)

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25 November 2017

J A Watts

1

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25 November 2017

A Watts

series ordinal

2

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25 November 2017

D A Middleton

series ordinal

3

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25 November 2017

language of work or name

English

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publication date

30 July 2001

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Journal of Biological Chemistry

25 November 2017

published in

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25 November 2017

volume

276

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25 November 2017

issue

46

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25 November 2017

page(s)

43197-43204

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Structure, transmembrane topology and helix packing of P-type ion pumps

25 November 2017

cites work

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Substitutions of serine 775 in the alpha subunit of the Na,K-ATPase selectively disrupt K+ high affinity activation without affecting Na+ interaction.

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21 January 2018

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Effects of mutations in M4 of the gastric H+,K+-ATPase on inhibition kinetics of SCH28080.

21 January 2018

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Comparison of covalent with reversible inhibitor binding sites of the gastric H,K-ATPase by site-directed mutagenesis

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Structural insights into the binding of cardiac glycosides to the digitalis receptor revealed by solid-state NMR

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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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Mutational analysis of putative SCH 28080 binding sites of the gastric H+,K+-ATPase

21 January 2018

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Transmembrane carboxyl residues are essential for cation-dependent function in the gastric H,K-ATPase

21 January 2018

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Glu-857 moderates K+-dependent stimulation and SCH 28080-dependent inhibition of the gastric H,K-ATPase

21 January 2018

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SCH28080 prevents omeprazole inhibition of the gastric H+/K+-ATPase

21 January 2018

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Ouabain interactions with the H5-H6 hairpin of the Na,K-ATPase reveal a possible inhibition mechanism via the cation binding domain

21 January 2018

1 reference

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The conformation of an inhibitor bound to the gastric proton pump

21 January 2018

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21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M104808200

1 reference

25 November 2017

1 reference