Ligand-binding residues integrate affinity and efficacy in the NMDA receptor

Molecular Pharmacology

Volumn 66, Issue 2, 2004, Pages 209-219

  Kalbaugh, Trisha L ^a   VanDongen, Hendrika M A ^a   VanDongen, Antonius M J ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

(2 AMINOETHYL)METHANETHIOSULFONATE; AMINO ACID; ASPARTIC ACID; CYCLOSERINE; CYSTEINE; GLUTAMATE RECEPTOR; GLUTAMIC ACID; GLYCINE; ION CHANNEL; N METHYL DEXTRO ASPARTIC ACID; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR STIMULATING AGENT; PARTIAL AGONIST; RECEPTOR SUBUNIT; SERINE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; COVALENT BOND; CRYSTALLOGRAPHY; DISSOCIATION CONSTANT; DRUG CONFORMATION; DRUG EFFICACY; DRUG RECEPTOR BINDING; FEMALE; HYDROGEN BOND; LIGAND BINDING; NONHUMAN; OOCYTE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; RECEPTOR AFFINITY; XENOPUS LAEVIS;

ANIMALS; BINDING SITES; ETHYL METHANESULFONATE; EXCITATORY AMINO ACID AGONISTS; LIGANDS; PHENOTYPE; PROTEIN CONFORMATION; PROTEIN STRUCTURE, TERTIARY; PROTEIN SUBUNITS; RECEPTORS, N-METHYL-D-ASPARTATE; XENOPUS LAEVIS;

EID: 3342967463     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: 10.1124/mol.66.2.209     Document Type: Article

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