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Scanning Mutagenesis of α-Conotoxin Vc1.1 Reveals Residues Crucial for Activity at the α9α10 Nicotinic Acetylcholine Receptor

Vc1.1 is a disulfide-rich peptide inhibitor of nicotinic acetylcholine receptors that has stimulated considerable interest in these receptors as potential therapeutic targets for the treatment of neuropathic pain. Here we present an extensive series of mutational studies in which all residues except...

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Detalhes bibliográficos
Main Authors: Halai, Reena, Clark, Richard J., Nevin, Simon T., Jensen, Jonas E., Adams, David J., Craik, David J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2740453/
https://ncbi.nlm.nih.gov/pubmed/19447885
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M109.015339
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