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http://purl.uniprot.org/citations/18310072http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18310072http://www.w3.org/2000/01/rdf-schema#comment"p94/calpain 3 is a skeletal muscle-specific Ca(2+)-regulated cysteine protease (calpain), and genetic loss of p94 protease activity causes muscular dystrophy (calpainopathy). In addition, a small in-frame deletion in the N2A region of connectin/titin that impairs p94-connectin interaction causes a severe muscular dystrophy (mdm) in mice. Since p94 via its interaction with the N2A and M-line regions of connectin becomes part of the connectin filament system that serves as a molecular scaffold for the myofibril, it has been proposed that structural and functional integrity of the p94-connectin complex is essential for health and maintenance of myocytes. In this study, we have surveyed the interactions made by p94 and connectin N2A inside COS7 cells. This revealed that p94 binds to connectin at multiple sites, including newly identified loci in the N2A and PEVK regions of connectin. Functionally, p94-N2A interactions suppress p94 autolysis and protected connectin from proteolysis. The connectin N2A region also contains a binding site for the muscle ankyrin repeat proteins (MARPs), a protein family involved in the cellular stress responses. MARP2/Ankrd2 competed with p94 for binding to connectin and was also proteolyzed by p94. Intriguingly, a connectin N2A fragment with the mdm deletion possessed enhanced resistance to proteases, including p94, and its interaction with MARPs was weakened. Our data support a model in which MARP2-p94 signaling converges within the N2A connectin segment and the mdm deletion disrupts their coordination. These results also implicate the dynamic nature of connectin molecule as a regulatory scaffold of p94 functions."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.org/dc/terms/identifier"doi:10.1074/jbc.m708262200"xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Mineki R."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Ono Y."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Tagami M."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Taguchi H."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Arai T."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Yanagida M."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Doi N."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Labeit D."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Labeit S."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Sorimachi H."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Kitamura F."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Hayashi C."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/author"Hirner S."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/name"J Biol Chem"xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/pages"14801-14814"xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/title"Multiple molecular interactions implicate the connectin/titin N2A region as a modulating scaffold for p94/calpain 3 activity in skeletal muscle."xsd:string
http://purl.uniprot.org/citations/18310072http://purl.uniprot.org/core/volume"283"xsd:string
http://purl.uniprot.org/citations/18310072http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18310072
http://purl.uniprot.org/citations/18310072http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18310072
http://purl.uniprot.org/uniprot/Q9CR42#attribution-44BC279E7C786891F781B03B1FBAF853http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/18310072
http://purl.uniprot.org/uniprot/Q9CR42#attribution-E678D166B7B8CD97DBEAE2C5944C91C3http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/18310072