An allosteric ligand-binding site in the extracellular cap of K2P channels
TREKs are members of the two-pore domain potassium (K2P) channels, being important clinical targets. Here the authors identify inhibitors of K2P that bind to an allosteric site located in their extracellular cap, suggesting that it might be a promising drug target for these channels.
Guardado en:
Autores principales: | Qichao Luo, Liping Chen, Xi Cheng, Yuqin Ma, Xiaona Li, Bing Zhang, Li Li, Shilei Zhang, Fei Guo, Yang Li, Huaiyu Yang |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/e10847ccfd6b420b8772f417a958f875 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Survey of solution dynamics in Src kinase reveals allosteric cross talk between the ligand binding and regulatory sites
por: Michael Tong, et al.
Publicado: (2017) -
Inhibitors of BRAF dimers using an allosteric site
por: Xiomaris M. Cotto-Rios, et al.
Publicado: (2020) -
Two distinct mechanisms for actin capping protein regulation--steric and allosteric inhibition.
por: Shuichi Takeda, et al.
Publicado: (2010) -
Integrated System for Purification and Assembly of PCV Cap Nano Vaccine Based on Targeting Peptide Ligand
por: Wang F, et al.
Publicado: (2020) -
A monoclonal antibody against KCNK9 K+ channel extracellular domain inhibits tumour growth and metastasis
por: Han Sun, et al.
Publicado: (2016)