The nucleotide-binding domains of sulfonylurea receptor 2A and 2B play different functional roles in nicorandil-induced activation of ATP-sensitive K+ Channels

Molecular Pharmacology

Volumn 65, Issue 5, 2004, Pages 1198-1207

  Yamada, Mitsuhiko ^a   Kurachi, Yoshihisa ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATE; NICORANDIL; NUCLEOTIDE DERIVATIVE; POTASSIUM CHANNEL; SULFONYLUREA RECEPTOR; SULFONYLUREA RECEPTOR 2A; SULFONYLUREA RECEPTOR 2B; UNCLASSIFIED DRUG;

ARTICLE; BINDING AFFINITY; CONCENTRATION RESPONSE; CONTROLLED STUDY; DNA BINDING; DRUG ACTIVITY; DRUG SENSITIVITY; ENZYME ACTIVATION; ENZYME ACTIVITY; GENE MUTATION; HUMAN; HUMAN CELL; HYDROLYSIS; MOLECULAR INTERACTION; PATCH CLAMP; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN MOTIF; WILD TYPE;

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATE; ALLOSTERIC SITE; ANIMALS; CELLS, CULTURED; ELECTROPHYSIOLOGY; HUMANS; LYSINE; MEMBRANE PROTEINS; MICE; MUTAGENESIS, SITE-DIRECTED; NICORANDIL; NUCLEOTIDES; POTASSIUM CHANNELS; RECOMBINANT PROTEINS;

EID: 2142663101     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: 10.1124/mol.65.5.1198     Document Type: Article

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