Molecular Determinants of Voltage-dependent Gating and Binding of Pore-blocking Drugs in Transmembrane Segment IIIS6 of the Na+ Channel α Subunit
Open Access
- 1 January 2001
- journal article
- Published by Elsevier
- Vol. 276 (1) , 20-27
- https://doi.org/10.1074/jbc.m006992200
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Hydrophobicity scales and computational techniques for detecting amphipathic structures in proteinsPublished by Elsevier ,2005
- The Structure of the Potassium Channel: Molecular Basis of K + Conduction and SelectivityScience, 1998
- Lamotrigine Versus Other Antiepileptic Drugs: A Star Rating System Is BornEpilepsia, 1994
- Auxiliary subunits of voltage-gated ion channelsNeuron, 1994
- LamotrigineDrugs, 1993
- Structural Basis of Amino Acid α Helix PropensityScience, 1993
- Hydrophobic Organization of Membrane ProteinsScience, 1989
- THE BACTERIAL PHOTOSYNTHETIC REACTION CENTER AS A MODEL FOR MEMBRANE PROTEINSAnnual Review of Biochemistry, 1989
- Antiarrhythmic Agents: The Modulated Receptor Mechanism of Action of Sodium and Calcium Channel-Blocking DrugsAnnual Review of Pharmacology and Toxicology, 1984
- Time- and voltage-dependent interactions of antiarrhythmic drugs with cardiac sodium channelsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1977