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http://purl.uniprot.org/citations/1648176http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1648176http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1648176http://www.w3.org/2000/01/rdf-schema#comment"Kainic acid is a potent neurotoxin for certain neurons. Its neurotoxicity is thought to be mediated by an excitatory amino-acid-gated ion channel (ionotropic receptor) possessing nanomolar affinity for kainate. Here we describe a new member of the rat excitatory amino-acid receptor gene family, KA-1, that has a 30% sequence similarity with the previously characterized alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptor subunits GluR-A to -D. The pharmacological profile of expressed recombinant KA-1 determined in binding experiments with [3H]kainate is different from that of the cloned AMPA receptors and similar to the mammalian high-affinity kainate receptor (kainate greater than quisqualate greater than glutamate much greater than AMPA) with a dissociation constant of about 5 nM for kainate. The selectively high expression of KA-1 messenger RNA in the CA3 region of the hippocampus closely corresponds to autoradiographically located high-affinity kainate binding sites. This correlation, as well as the particular in vivo pattern of neurodegeneration observed on kainate-induced neurotoxicity, suggests that KA-1 participates in receptors mediating the kainate sensitivity of neurons in the central nervous system."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.org/dc/terms/identifier"doi:10.1038/351742a0"xsd:string
http://purl.uniprot.org/citations/1648176http://purl.org/dc/terms/identifier"doi:10.1038/351742a0"xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Werner P."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Werner P."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Seeburg P.H."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Seeburg P.H."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Wisden W."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Wisden W."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Voigt M."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Voigt M."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Keinaenen K."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/author"Keinaenen K."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/date"1991"xsd:gYear
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/date"1991"xsd:gYear
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/name"Nature"xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/name"Nature"xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/pages"742-744"xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/pages"742-744"xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/title"Cloning of a putative high-affinity kainate receptor expressed predominantly in hippocampal CA3 cells."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/title"Cloning of a putative high-affinity kainate receptor expressed predominantly in hippocampal CA3 cells."xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/volume"351"xsd:string
http://purl.uniprot.org/citations/1648176http://purl.uniprot.org/core/volume"351"xsd:string