Molecular Determinants of High Affinity Phenylalkylamine Block of l-type Calcium Channels in Transmembrane Segment IIIS6 and the Pore Region of the α1Subunit
Open Access
- 1 July 1997
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 272 (30), 18759-18765
- https://doi.org/10.1074/jbc.272.30.18759
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Analysis of the Dihydropyridine Receptor Site ofl-type Calcium Channels by Alanine-scanning MutagenesisPublished by Elsevier ,1997
- Two Amino Acid Residues in the IIIS5 Segment of L-Type Calcium Channels Differentially Contribute to 1,4-Dihydropyridine SensitivityJournal of Biological Chemistry, 1996
- Identification of Benz(othi)azepine-binding Regions within L-type Calcium Channel α1 SubunitsPublished by Elsevier ,1996
- Transfer of L-type Calcium Channel IVS6 Segment Increases Phenylalkylamine Sensitivity of α1APublished by Elsevier ,1996
- Transfer of 1,4-Dihydropyridine Sensitivity from L-Type to Class A (BI) Calcium ChannelsNeuron, 1996
- Molecular properties of a superfamily of plasma-membrane cation channelsCurrent Opinion in Cell Biology, 1994
- Structural Basis of Amino Acid α Helix PropensityScience, 1993
- Cloning and tissue‐specific expression of the brain calcium channel β‐subunitFEBS Letters, 1991
- Distinct calcium channels are generated by alternative splicing and are differentially expressed in the mammalian CNSNeuron, 1991
- Molecular Pharmacology of the Calcium ChannelJournal of Cardiovascular Pharmacology, 1984