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http://purl.uniprot.org/citations/23566939http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23566939http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23566939http://www.w3.org/2000/01/rdf-schema#comment"High polymorphism is one of the most important features of human leukocyte antigen (HLA) alleles, which were initially classified by serotyping but have recently been re-grouped into supertypes according to their peptide presentation properties. Two relatively prevalent HLA alleles HLA-A*6801 and HLA-A*6802, are classified into the same serotype HLA-A68. However, based on their distinct peptide-binding characteristics, HLA-A*6801 is grouped into A3 supertype, whereas HLA-A*6802 belongs to A2 supertype, similar to HLA-A*0201. Thusfar, the structural basis of the different supertype definitions of these serotyping-identical HLA alleles remains largely unknown. Herein, we determined the structures of HLA-A*6801 and HLA-A*6802 presenting three typical A3 and A2 supertype-restricted peptides, respectively. The binding capabilities of these peptides to HLA-A*6801, HLA-A*6802, and HLA-A*0201 were analyzed. These data indicate that the similar conformations of the residues within the F pocket contribute to close-related peptide binding features of HLA-A*6802 and HLA-A*0201. However, the overall structure and the peptide conformation of HLA-A*6802 are more similar to HLA-A*6801 rather than HLA-A*0201 which illuminates the similar serotype grouping of HLA-A*6802 and HLA-A*6801. Our findings are helpful for understanding the divergent peptide presentation and virus-specific CTL responses impacted by MHC micropolymorphisms and also elucidate the molecular basis of HLA supertype definitions."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.org/dc/terms/identifier"doi:10.1016/j.molimm.2013.03.015"xsd:string
http://purl.uniprot.org/citations/23566939http://purl.org/dc/terms/identifier"doi:10.1016/j.molimm.2013.03.015"xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Cheng H."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Cheng H."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Gao G.F."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Gao G.F."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Liu J."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Liu J."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Qi J."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Qi J."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Niu L."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Niu L."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Zhang Y."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Zhang Y."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Zhang S."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Zhang S."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Tan S."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/author"Tan S."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/name"Mol. Immunol."xsd:string
http://purl.uniprot.org/citations/23566939http://purl.uniprot.org/core/name"Mol Immunol"xsd:string