Sequence Differences between α1C and α1S Ca2+ Channel Subunits Reveal Structural Determinants of a Guarded and Modulated Benzothiazepine Receptor-Reference-Cited by-同舟云学术

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Sequence Differences between α1C and α1S Ca2+ Channel Subunits Reveal Structural Determinants of a Guarded and Modulated Benzothiazepine Receptor

Published:1999-03 Issue:10 Volume:274 Page:6154-6160
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Berjukow Stanislav,Gapp Franz,Aczél Stefan,Sinnegger Martina J.,Mitterdorfer Joerg,Glossmann Hartmut,Hering Steffen

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference32 articles.

1. The naming of voltage-gated calcium channels

2. MOLECULAR DETERMINANTS OF DRUG BINDING AND ACTION ON L-TYPE CALCIUM CHANNELS

3. Structural basis of drug binding to L Ca2+ channels

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

5. Molecular Determinants of High Affinity Dihydropyridine Binding in L-type Calcium Channels

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1. T1143 essential for CaV1.2 inhibition by diltiazem;European Journal of Pharmacology;2021-03

2. Selective pressure modulation of synaptic voltage‐dependent calcium channels—involvement in HPNS mechanism;Journal of Cellular and Molecular Medicine;2016-06-08

3. Selective modulation of cellular voltage-dependent calcium channels by hyperbaric pressureâ€”a suggested HPNS partial mechanism;Frontiers in Cellular Neuroscience;2014-05-27

4. Interaction of diltiazem with an intracellularly accessible binding site on CaV1.2;British Journal of Pharmacology;2011-01-28

5. Molecular Modeling of Benzothiazepine Binding in the L-type Calcium Channel;Journal of Biological Chemistry;2008-06

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