L-Type Calcium Channels: Binding Domains for Dihydropyridines and Benzothiazepines Are Located in Close Proximity to Each Other-Reference-Cited by-同舟云学术

L-Type Calcium Channels: Binding Domains for Dihydropyridines and Benzothiazepines Are Located in Close Proximity to Each Other

Published:1997-03-01 Issue:12 Volume:36 Page:3625-3631
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Brauns Thomas¹,Prinz Heino¹,Kimball S. David¹,Haugland Richard P.¹,Striessnig Jörg¹,Glossmann Hartmut¹

Affiliation:

1. Institut für Biochemische Pharmakologie, Peter-Mayr-Strasse 1, A-6020 Innsbruck, Austria, Max-Planck-Institut für Molekulare Physiologie, Rheinlanddamm 201, D-44139 Dortmund, Germany, Bristol-Myers Squibb Pharmaceutical Research Institute, P.O. Box 4000, Princeton, New Jersey 08543-4000, and Molecular Probes, Eugene, Oregon 97402-0414

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi9613584

Reference32 articles.

1. Complex Molecular Mechanism for Dihydropyridine Binding to L-Type Ca2+-Channels As Revealed by Fluorescence Resonance Energy Transfer

2. The naming of voltage-gated calcium channels

3. Benzothiazepinone Binding Domain of Purified L-Type Calcium Channels: Direct Labeling Using a Novel Fluorescent Diltiazem Analog

4. Transfer of L-type Calcium Channel IVS6 Segment Increases Phenylalkylamine Sensitivity of α1A

5. Structural Model of the Outer Vestibule and Selectivity Filter of the Shaker Voltage-gated K + Channel

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