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http://purl.uniprot.org/citations/19808674http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19808674http://www.w3.org/2000/01/rdf-schema#comment"Earlier studies have demonstrated interaction of the murine major histocompatibility complex (MHC) class I molecule K(d) with amyloid precursor-like protein 2 (APLP2), a ubiquitously expressed member of the amyloid precursor protein family. Our current findings indicate that APLP2 is internalized in a clathrin-dependent manner, as shown by utilization of inhibitors of the clathrin pathway. Furthermore, we demonstrated that APLP2 and K(d) bind at the cell surface and are internalized together. The APLP2 cytoplasmic tail contains two overlapping consensus motifs for binding to the adaptor protein-2 complex, and mutation of a tyrosine shared by both motifs severely impaired APLP2 internalization and ability to promote K(d) endocytosis. Upon increased expression of wild type APLP2, K(d) molecules were predominantly directed to the lysosomes rather than recycled to the plasma membrane. These findings suggest a model in which APLP2 binds K(d) at the plasma membrane, facilitates uptake of K(d) in a clathrin-dependent manner, and routes the endocytosed K(d) to the lysosomal degradation pathway. Thus, APLP2 has a multistep trafficking function that influences the expression of major histocompatibility complex class I molecules at the plasma membrane."xsd:string
http://purl.uniprot.org/citations/19808674http://purl.org/dc/terms/identifier"doi:10.1074/jbc.m109.039727"xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/author"Sharma M."xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/author"Caplan S."xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/author"Naslavsky N."xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/author"Tuli A."xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/author"Solheim J.C."xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/author"Capek H.L."xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/date"2009"xsd:gYear
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/name"J Biol Chem"xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/pages"34296-34307"xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/title"Mechanism for amyloid precursor-like protein 2 enhancement of major histocompatibility complex class I molecule degradation."xsd:string
http://purl.uniprot.org/citations/19808674http://purl.uniprot.org/core/volume"284"xsd:string
http://purl.uniprot.org/citations/19808674http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/19808674
http://purl.uniprot.org/citations/19808674http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/19808674
http://purl.uniprot.org/uniprot/#_A0A140VJE9-mappedCitation-19808674http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19808674
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http://purl.uniprot.org/uniprot/#_Q06481-mappedCitation-19808674http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19808674
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http://purl.uniprot.org/uniprot/#_Q9UED0-mappedCitation-19808674http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19808674
http://purl.uniprot.org/uniprot/Q9UED0http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/19808674
http://purl.uniprot.org/uniprot/Q06481http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/19808674