Cargando…
Identification of a druggable pocket of the calcium-activated chloride channel TMEM16A in its open state
The calcium-activated chloride channel TMEM16A is a potential drug target to treat hypertension, secretory diarrhea, and several cancers. However, all reported TMEM16A structures are either closed or desensitized, and direct inhibition of the open state by drug molecules lacks a reliable structural...
Autores principales: | Shi, Sai, Ma, Biao, Ji, Qiushuang, Guo, Shuai, An, Hailong, Ye, Sheng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245117/ https://www.ncbi.nlm.nih.gov/pubmed/37142220 http://dx.doi.org/10.1016/j.jbc.2023.104780 |
Ejemplares similares
-
Theaflavin binds to a druggable pocket of TMEM16A channel and inhibits lung adenocarcinoma cell viability
por: Shi, Sai, et al.
Publicado: (2021) -
Recent progress in structural studies on TMEM16A channel
por: Shi, Sai, et al.
Publicado: (2020) -
Mechanism of pore opening in the calcium-activated chloride channel TMEM16A
por: Lam, Andy K. M., et al.
Publicado: (2021) -
Voltage-Dependent Protonation of the Calcium Pocket Enable Activation of the Calcium-Activated Chloride Channel Anoctamin-1 (TMEM16A)
por: Segura-Covarrubias, Guadalupe, et al.
Publicado: (2020) -
Activation and Inhibition of TMEM16A Calcium-Activated Chloride Channels
por: Ni, Yu-Li, et al.
Publicado: (2014)