Residue Phe266 in S5-S6 loop is not critical for Charybdotoxin binding to Ca2+-activated K+ (mSlo1) channels

Acta Pharmacologica Sinica

Volumn 27, Issue 7, 2006, Pages 945-949

  Yao, Jing ^a   Li, Hui ^a   Gan, Ge Liang ^a   Wu, Ying ^a   Ding, Jiu Ping ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Charybdotoxin; Large conductance calcium activated potassium channelss; Slo1

Indexed keywords

CALCIUM ACTIVATED POTASSIUM CHANNEL; CHARYBDOTOXIN; MUTANT PROTEIN; PHENYLALANINE;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DISSOCIATION CONSTANT; DRUG INHIBITION; DRUG PROTEIN BINDING; NONHUMAN; OOCYTE; PROTEIN BINDING; PROTEIN EXPRESSION; SITE DIRECTED MUTAGENESIS; XENOPUS;

AMINO ACID SEQUENCE; ANIMALS; CHARYBDOTOXIN; FEMALE; LARGE-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNEL ALPHA SUBUNITS; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; MUTATION; NEUROTOXINS; OOCYTES; PROTEIN BINDING; XENOPUS LAEVIS;

EID: 33748532508     PISSN: 16714083     EISSN: 17457254     Source Type: Journal    
DOI: 10.1111/j.1745-7254.2006.00385.x     Document Type: Article

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