Silencing of the constitutive activity of the dopamine D1B receptor: Reciprocal mutations between D1 receptor subtypes delineate residues underlying activation properties

Journal of Biological Chemistry

Volumn 271, Issue 45, 1996, Pages 28071-28076

  Charpentier, Stéphane ^a   Jarvie, Keith R ^a   Severynse, Diana M ^a   Caron, Marc G ^a   Tiberi, Mario ^a,b  

^a DUKE UNIVERSITY   (United States)

^b OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DOPAMINE 1 RECEPTOR; RECEPTOR SUBTYPE;

ARTICLE; DOPAMINERGIC SYSTEM; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN STRUCTURE; RECEPTOR BINDING; SITE DIRECTED MUTAGENESIS; STRUCTURE ANALYSIS;

(R)-2,3,4,5-TETRAHYDRO-8-CHLORO-3-METHYL-5-PHENYL-1H-3-BENZAZEPIN-7-OL; ADENYLATE CYCLASE; ARGININE; BINDING, COMPETITIVE; BUTACLAMOL; CYCLIC AMP; DOPAMINE; DOSE-RESPONSE RELATIONSHIP, DRUG; HUMANS; ISOLEUCINE; MODELS, MOLECULAR; PHENYLALANINE; PROTEIN CONFORMATION; RECEPTORS, DOPAMINE D1; RECEPTORS, DOPAMINE D5; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0029903521     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.271.45.28071     Document Type: Article

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