Exploring Kv1.2 Channel Inactivation Through MD Simulations and Network Analysis
The KCNA2 gene encodes the Kv1.2 channel, a mammalian Shaker-like voltage-gated K+ channel, whose defections are linked to neuronal deficiency and childhood epilepsy. Despite the important role in the kinetic behavior of the channel, the inactivation remained hereby elusive. Here, we studied the Kv1...
| Published in: | Frontiers in Molecular Biosciences |
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| Main Authors: | , , |
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2021-12-01
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| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fmolb.2021.784276/full |
