Cargando…
The Trials and Tribulations of Structure Assisted Design of K(Ca) Channel Activators
Calcium-activated K(+) channels constitute attractive targets for the treatment of neurological and cardiovascular diseases. To explain why certain 2-aminobenzothiazole/oxazole-type K(Ca) activators (SKAs) are K(Ca)3.1 selective we previously generated homology models of the C-terminal calmodulin-bi...
Autores principales: | Shim, Heesung, Brown, Brandon M., Singh, Latika, Singh, Vikrant, Fettinger, James C., Yarov-Yarovoy, Vladimir, Wulff, Heike |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764326/ https://www.ncbi.nlm.nih.gov/pubmed/31616290 http://dx.doi.org/10.3389/fphar.2019.00972 |
Ejemplares similares
-
New capsaicin analogs as molecular rulers to define the permissive conformation of the mouse TRPV1 ligand-binding pocket
por: Vu, Simon, et al.
Publicado: (2020) -
Towards Structure-Guided Development of Pain Therapeutics Targeting Voltage-Gated Sodium Channels
por: Nguyen, Phuong T., et al.
Publicado: (2022) -
Structural modeling of hERG channel–drug interactions using Rosetta
por: Emigh Cortez, Aiyana M., et al.
Publicado: (2023) -
Are there superagonists for calcium-activated potassium channels?
por: Brown, Brandon M., et al.
Publicado: (2017) -
Molecular determinants of μ-conotoxin KIIIA interaction with the human voltage-gated sodium channel Na(V)1.7
por: Kimball, Ian H., et al.
Publicado: (2023)