Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-18571
Neuron 1996 Feb 01;162:399-406. doi: 10.1016/s0896-6273(00)80057-4.
Show Gene links Show Anatomy links

Agitoxin footprinting the shaker potassium channel pore.

Gross A , MacKinnon R .


???displayArticle.abstract???
In voltage-dependent K+ channels, each of the four identical subunits contributes one pore loop to the central ion selectivity unit at the interface between the subunits. The pore loop is also the target for scorpion venom peptide inhibitors. These inhibitors bind at the pore entryway between the four subunits and can assume any one of four orientations. The orientations become distinguishable only if the binding site symmetry is disrupted. We have used mutagenesis and site-directed chemical modification to alter pore loop amino acids in either one or four subunits. The effects of these alterations on inhibitor affinity define the eccentricity of amino acids in the pore entryway and imply a different secondary structure for the amino and carboxyl ends of the pore loop.

???displayArticle.pubmedLink??? 8789954
???displayArticle.link??? Neuron
???displayArticle.grants??? [+]