The NR1 M3 domain mediates allosteric coupling in the N-Methyl-D-aspartate receptor

Molecular Pharmacology

Volumn 74, Issue 2, 2008, Pages 454-465

  Blanke, Marie L ^a,b   VanDongen, Antonius M J ^b  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b DUKE NUS MEDICAL SCHOOL   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE; GLUTAMIC ACID; GLYCINE; MUTANT PROTEIN; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR 1; PROTEIN SUBUNIT;

ALLOSTERISM; AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CHANNEL GATING; COMPETITIVE INHIBITION; COUPLING FACTOR; LIGAND BINDING; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN DOMAIN;

ALLOSTERIC REGULATION; ANIMALS; BINDING SITES; EXCITATORY AMINO ACID ANTAGONISTS; FEMALE; PROTEIN INTERACTION DOMAINS AND MOTIFS; RECEPTORS, N-METHYL-D-ASPARTATE; XENOPUS LAEVIS;

EID: 47949104957     PISSN: 0026895X     EISSN: 15210111     Source Type: Journal    
DOI: 10.1124/mol.107.044115     Document Type: Article

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