Rauer, H <br/><br/>
Structure-guided transformation of charybdotoxin yields an analog that selectively targets Ca(2+)-activated over voltage-gated K(+) channels.  [electronic resource] 

 -  The Journal of biological chemistry  Jan 2000 
 - 1201-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0021-9258 
<br/><br/><label>Standard No.: </label>10.1074/jbc.275.2.1201  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Bacterial Proteins--chemistry<br/>Binding Sites<br/>Calcium Channels--chemistry<br/>Cell Line<br/>Charybdotoxin--chemistry<br/>Drug Design<br/>Humans<br/>Intermediate-Conductance Calcium-Activated Potassium Channels<br/>Kv1.3 Potassium Channel<br/>Models, Molecular<br/>Molecular Sequence Data<br/>Potassium Channels--chemistry<br/>Potassium Channels, Voltage-Gated<br/>Protein Conformation<br/>Protein Structure, Secondary<br/>Rats<br/>Recombinant Proteins--chemistry<br/>Sequence Alignment<br/>T-Lymphocytes--physiology<br/>Transfection