Molecular mechanism of calcium channel block by isradipine. Role of a drug-induced inactivated channel conformation (Q48892866)

16 February 2018

title

Molecular mechanism of calcium channel block by isradipine. Role of a drug-induced inactivated channel conformation (English)

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16 February 2018

author name string

Berjukow S

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16 February 2018

Marksteiner R

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Gapp F

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16 February 2018

Sinnegger MJ

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Hering S

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16 February 2018

language of work or name

English

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publication date

1 July 2000

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16 February 2018

Journal of Biological Chemistry

published in

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volume

275

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issue

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page(s)

22114-22120

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Nine L-type amino acid residues confer full 1,4-dihydropyridine sensitivity to the neuronal calcium channel alpha1A subunit. Role of L-type Met1188.

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Molecular determinants of drug binding and action on L-type calcium channels

21 January 2018

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Molecular localization of regions in the L-type calcium channel critical for dihydropyridine action

21 January 2018

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Analysis of the Dihydropyridine Receptor Site ofl-type Calcium Channels by Alanine-scanning Mutagenesis

21 January 2018

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Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction

21 January 2018

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Nitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated state

21 January 2018

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Alternatively Spliced IS6 Segments of the α 1C Gene Determine the Tissue-Specific Dihydropyridine Sensitivity of Cardiac and Vascular Smooth Muscle L-Type Ca 2+ Channels

21 January 2018

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Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel

21 January 2018

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Ca2+ channel sensitivity towards the blocker isradipine is affected by alternative splicing of the human alpha1C subunit gene

21 January 2018

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Reconstruction of the dihydropyridine site in a non-L-type calcium channel: the role of the IS6 segment

21 January 2018

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Molecular studies on the voltage dependence of dihydropyridine action on L-type Ca2+ channels. Critical involvement of tyrosine residues in motif IIIS6 and IVS6.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M908836199

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16 February 2018

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16 February 2018