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Understanding pH-Dependent Selectivity of Alamethicin K18 Channels by Computer Simulation

Alamethicin K18 is a covalently linked alamethicin dimer in which the glutamine residue at position 18 in each helix has been replaced by a lysine residue. As described in previous work, channels formed by this peptide show pH-dependent selectivity. The maximum anion selectivity of the putative octa...

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Detalhes bibliográficos
Main Authors: Tieleman, D. Peter, Borisenko, Vitali, Sansom, Mark S. P., Woolley, G. Andrew
Formato: Artigo
Idioma:Inglês
Publicado em: Biophysical Society 2003
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1302720/
https://ncbi.nlm.nih.gov/pubmed/12609853
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