Chen, Jun <br/><br/>
Position of aromatic residues in the S6 domain, not inactivation, dictates cisapride sensitivity of HERG and eag potassium channels.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Sep 2002 
 - 12461-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.192367299  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Amino Acids, Aromatic--chemistry<br/>Animals<br/>Binding Sites--genetics<br/>Cation Transport Proteins<br/>Cisapride--pharmacology<br/>DNA-Binding Proteins<br/>Drosophila Proteins--antagonists & inhibitors<br/>ERG1 Potassium Channel<br/>Ether-A-Go-Go Potassium Channels<br/>Female<br/>Humans<br/>In Vitro Techniques<br/>Long QT Syndrome--chemically induced<br/>Membrane Potentials<br/>Molecular Sequence Data<br/>Mutagenesis, Site-Directed<br/>Oocytes--metabolism<br/>Potassium Channel Blockers<br/>Potassium Channels--chemistry<br/>Potassium Channels, Voltage-Gated<br/>Protein Structure, Tertiary<br/>Recombinant Proteins--antagonists & inhibitors<br/>Sequence Homology, Amino Acid<br/>Trans-Activators<br/>Transcriptional Regulator ERG<br/>Xenopus laevis