Molecular modeling of the tetramerization domain of human potassium channel Kv10.2 in different oligomeric states
- 作者: Novoseletsky V.N.1, Volyntseva A.D.1, Shaitan K.V.1, Sokolova O.S.1
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隶属关系:
- Department of Biology
- 期: 卷 72, 编号 2 (2017)
- 页面: 69-73
- 栏目: Molecular Biology
- URL: https://journal-vniispk.ru/0096-3925/article/view/173608
- DOI: https://doi.org/10.3103/S0096392517020031
- ID: 173608
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详细
A voltage-gated potassium channel Kv10.2 is expressed in the nervous system, but its functions and involvement in the development of human disease remain poorly understood. Mutant forms of the Kv10.2 channel were found in patients with epileptic encephalopathy and autism. Molecular modeling of the channel spatial structure is an important tool for gaining knowledge about the molecular aspects of the channel functioning and mechanisms responsible for pathogenesis. In the present work, molecular modeling of the helical fragment of the human Kv10.2 (hEAG2) C-terminal domain in dimeric, trimeric, and tetrameric forms was performed. The stability of all forms was confirmed by molecular dynamics simulation. Contacts and interactions, stabilizing the structure, were identified.
作者简介
V. Novoseletsky
Department of Biology
编辑信件的主要联系方式.
Email: valeryns@gmail.com
俄罗斯联邦, Moscow, 119234
A. Volyntseva
Department of Biology
Email: valeryns@gmail.com
俄罗斯联邦, Moscow, 119234
K. Shaitan
Department of Biology
Email: valeryns@gmail.com
俄罗斯联邦, Moscow, 119234
O. Sokolova
Department of Biology
Email: valeryns@gmail.com
俄罗斯联邦, Moscow, 119234
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