Pore accessibility during C-type inactivation in Shaker K+ channels
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/S0014-5793(98)00635-8/fullpdf
Reference18 articles.
1. Current inactivation involves a histidine residue in the pore of the rat lymphocyte potassium channel RGK5
2. Two types of inactivation in Shaker K+ channels: Effects of alterations in the carboxy-terminal region
3. Pore mutations in Shaker K+ channels distinguish between the sites of tetraethylammonium blockade and C-type inactivation.
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1. A distinct mechanism of C-type inactivation in the Kv-like KcsA mutant E71V;Nature Communications;2022-03-23
2. A different mechanism of C-type inactivation in the Kv-like KcsA mutant E71V;2021-09-22
3. Kinetic analysis of the effects of H+or Ni2+on Kv1.5 current shows that both ions enhance slow inactivation and induce resting inactivation;The Journal of Physiology;2010-08-13
4. Charade of the SR K+-Channel: Two Ion-Channels, TRIC-A and TRIC-B, Masquerade as a Single K+-Channel;Biophysical Journal;2010-07
5. Slow Inactivation in Shaker K Channels Is Delayed by Intracellular Tetraethylammonium;Journal of General Physiology;2008-11-24
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