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Volumn 77, Issue 2, 2001, Pages 445-451
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Identification of amino acid residues responsible for the α5 subunit binding selectivity of L-655,708, a benzodiazepine binding site ligand at the GABAA receptor
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Author keywords
Benzodiazepine binding site; GABAA receptor; Site directed mutagenesis
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Indexed keywords
4 AMINOBUTYRIC ACID A RECEPTOR;
AMINO ACID;
BENZODIAZEPINE;
L 655 708;
LIGAND;
UNCLASSIFIED DRUG;
ALPHA CHAIN;
AMINO TERMINAL SEQUENCE;
ARTICLE;
BINDING AFFINITY;
BINDING SITE;
CONTROLLED STUDY;
DRUG BINDING;
DRUG SELECTIVITY;
HUMAN;
HUMAN CELL;
LIGAND BINDING;
MOLECULAR BIOLOGY;
PRIORITY JOURNAL;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
ANIMALS;
ANTI-ANXIETY AGENTS;
AZIDES;
BENZODIAZEPINES;
BINDING SITES;
BINDING, COMPETITIVE;
CARBOLINES;
DNA, COMPLEMENTARY;
FEMALE;
FLUMAZENIL;
FLUNITRAZEPAM;
HUMANS;
IMIDAZOLES;
ISOLEUCINE;
LIGANDS;
MOLECULAR SEQUENCE DATA;
MUTAGENESIS, SITE-DIRECTED;
OOCYTES;
PROTEIN BINDING;
PROTEIN STRUCTURE, TERTIARY;
PROTEIN SUBUNITS;
PYRIDAZINES;
PYRIDINES;
RECEPTORS, GABA-A;
RECOMBINANT FUSION PROTEINS;
SEQUENCE ALIGNMENT;
STRUCTURE-ACTIVITY RELATIONSHIP;
THREONINE;
TRANSFECTION;
XENOPUS LAEVIS;
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EID: 0035044472
PISSN: 00223042
EISSN: None
Source Type: Journal
DOI: 10.1046/j.1471-4159.2001.00289.x Document Type: Article |
Times cited : (55)
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References (23)
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