The molecular basis for an allosteric inhibition of K+-flux gating in K2P channels
<p>Two-pore-domain potassium (K<sub>2P</sub>) channels are key regulators of many physiological and pathophysiological processes and thus emerged as promising drug targets. As for other potassium channels, there is a lack of selective blockers, since drugs preferentially bind to a...
| Main Authors: | , , , , , , , , , , , , |
|---|---|
| פורמט: | Journal article |
| שפה: | English |
| יצא לאור: |
eLife Sciences Publications
2019
|