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Gambierol and n-alkanols inhibit Shaker Kv channel via distinct binding sites outside the K(+) pore

The marine polycyclic-ether toxin gambierol and 1-butanol (n-alkanol) inhibit Shaker-type K(v) channels by interfering with the gating machinery. Competition experiments indicated that both compounds do not share an overlapping binding site but gambierol is able to affect 1-butanol affinity for Shak...

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Detalhes bibliográficos
Publicado no:Toxicon
Main Authors: Martínez-Morales, Evelyn, Kopljar, Ivan, Rainier, Jon D., Tytgat, Jan, Snyders, Dirk J., Labro, Alain J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7008702/
https://ncbi.nlm.nih.gov/pubmed/27475861
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.toxicon.2016.07.017
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