Characterization of binding site of closed-state KCNQ1 potassium channel by homology modeling, molecular docking, and pharmacophore identification

Author:

Du Lü-Pei,Li Min-Yong,Tsai Keng-Chang,You Qi-Dong,Xia Lin

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference32 articles.

1. Molecular physiology of cardiac delayed rectifier K+ channels;Sanguinetti;Heart Vessels Suppl.,1997

2. Is the slowly activating component of the delayed rectifier current, IKs’ absent from undiseased human ventricular myocardium?;Veldkamp;Cardiovasc. Res.,1998

3. The cardiac K+ channel KCNQ1 is essential for gastric acid secretion;Grahammer;Gastroenterology,2001

4. IKs, a slow and intriguing cardiac K+ channel and its associated long QT diseases;Barhanin;Trends Cardiovasc. Med.,1998

5. Molecular determinants of KCNQ1 channel block by a benzodiazepine;Seebohm;Mol. Pharmacol.,2003

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