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http://purl.uniprot.org/citations/23754381http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23754381http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23754381http://www.w3.org/2000/01/rdf-schema#comment"The scaffolding protein at the neuromuscular junction, rapsyn, enables clustering of nicotinic acetylcholine receptors in high concentration and is critical for muscle function. Patients with insufficient receptor clustering suffer from muscle weakness. However, the detailed organization of the receptor-rapsyn network is poorly understood: it is unclear whether rapsyn first forms a wide meshwork to which receptors can subsequently dock or whether it only forms short bridges linking receptors together to make a large cluster. Furthermore, the number of rapsyn-binding sites per receptor (a heteropentamer) has been controversial. Here, we show by cryoelectron tomography and subtomogram averaging of Torpedo postsynaptic membrane that receptors are connected by up to three rapsyn bridges, the minimum number required to form a 2D network. Half of the receptors belong to rapsyn-connected groups comprising between two and fourteen receptors. Our results provide a structural basis for explaining the stability and low diffusion of receptors within clusters."xsd:string
http://purl.uniprot.org/citations/23754381http://purl.org/dc/terms/identifier"doi:10.1073/pnas.1301277110"xsd:string
http://purl.uniprot.org/citations/23754381http://purl.org/dc/terms/identifier"doi:10.1073/pnas.1301277110"xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/author"Unwin N."xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/author"Unwin N."xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/author"Zuber B."xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/author"Zuber B."xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/name"Proc Natl Acad Sci U S A"xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/pages"10622-10627"xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/pages"10622-10627"xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/title"Structure and superorganization of acetylcholine receptor-rapsyn complexes."xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/title"Structure and superorganization of acetylcholine receptor-rapsyn complexes."xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/volume"110"xsd:string
http://purl.uniprot.org/citations/23754381http://purl.uniprot.org/core/volume"110"xsd:string
http://purl.uniprot.org/citations/23754381http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23754381
http://purl.uniprot.org/citations/23754381http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23754381
http://purl.uniprot.org/citations/23754381http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23754381
http://purl.uniprot.org/citations/23754381http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23754381
http://purl.uniprot.org/uniprot/Q6S3H9http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/23754381
http://purl.uniprot.org/uniprot/Q6S3H8http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/23754381