Mechanism of Dihydropyridine Interaction with Critical Binding Residues of L-type Ca2+ Channel α1 Subunits
Open Access
- 1 April 2001
- journal article
- Published by Elsevier BV
- Vol. 276 (16), 12730-12735
- https://doi.org/10.1074/jbc.m010164200
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Serine Residue in the IIIS5-S6 Linker of the L-type Ca2+ Channel α1C Subunit Is the Critical Determinant of the Action of Dihydropyridine Ca2+Channel AgonistsPublished by Elsevier BV ,2000
- Three New Familial Hemiplegic Migraine Mutants Affect P/Q-type Ca2+ Channel KineticsPublished by Elsevier BV ,2000
- Molecular Mechanism of Diltiazem Interaction with L-type Ca2+ ChannelsJournal of Biological Chemistry, 1998
- The Structure of the Potassium Channel: Molecular Basis of K + Conduction and SelectivityScience, 1998
- Analysis of the Dihydropyridine Receptor Site ofl-type Calcium Channels by Alanine-scanning MutagenesisPublished by Elsevier BV ,1997
- Motif III S5 of L-type Calcium Channels Is Involved in the Dihydropyridine Binding SitePublished by Elsevier BV ,1997
- Transfer of 1,4-Dihydropyridine Sensitivity from L-Type to Class A (BI) Calcium ChannelsNeuron, 1996
- Distinct calcium channels are generated by alternative splicing and are differentially expressed in the mammalian CNSNeuron, 1991
- Primary Structure of the β Subunit of the DHP-Sensitive Calcium Channel from Skeletal MuscleScience, 1989
- Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extensionGene, 1989