Molecular modeling of the tetramerization domain of human potassium channel Kv10.2 in different oligomeric states


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

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

补充文件

附件文件
动作
1. JATS XML

版权所有 © Allerton Press, Inc., 2017