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http://purl.uniprot.org/citations/7489366http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7489366http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7489366http://www.w3.org/2000/01/rdf-schema#comment"The molecular recognition theory suggests that binding sites of interacting proteins, for example, peptide hormone and its receptor binding site, were originally encoded by and evolved from complementary strands of genomic DNA. To test this theory, we screened a rat kidney complementary DNA library twice: first with the angiotensin II (AII) followed by the vasopressin (AVP) antisense oligonucleotide probe, expecting to isolate cDNA clones of the respective receptors. Surprisingly, the identical cDNA clone was isolated twice independently. Structural analysis revealed a single receptor polypeptide with seven predicted transmembrane regions, distinct AII and AVP putative binding domains, a Gs protein-activation motif, and an internalization recognition sequence. Functional analysis revealed specific binding to both AII and AVP as well as AII- and AVP-induced coupling to the adenylate cyclase second messenger system. Site-directed mutagenesis of the predicted AII binding domain obliterates AII binding but preserves AVP binding. This corroborates the dual nature of the receptor and provides direct molecular genetic evidence for the molecular recognition theory."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.org/dc/terms/identifier"doi:10.1038/nm1095-1074"xsd:string
http://purl.uniprot.org/citations/7489366http://purl.org/dc/terms/identifier"doi:10.1038/nm1095-1074"xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/author"Akimoto K."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/author"Akimoto K."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/author"Ruiz-Opazo N."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/author"Ruiz-Opazo N."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/author"Herrera V.L.M."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/author"Herrera V.L.M."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/date"1995"xsd:gYear
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/date"1995"xsd:gYear
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/name"Nat. Med."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/name"Nat. Med."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/pages"1074-1081"xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/pages"1074-1081"xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/title"Identification of a novel dual angiotensin II/vasopressin receptor on the basis of molecular recognition theory."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/title"Identification of a novel dual angiotensin II/vasopressin receptor on the basis of molecular recognition theory."xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/volume"1"xsd:string
http://purl.uniprot.org/citations/7489366http://purl.uniprot.org/core/volume"1"xsd:string
http://purl.uniprot.org/citations/7489366http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7489366
http://purl.uniprot.org/citations/7489366http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7489366
http://purl.uniprot.org/citations/7489366http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7489366
http://purl.uniprot.org/citations/7489366http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7489366