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• W2082607788 endingPage "1037" @default.
• W2082607788 startingPage "1029" @default.
• W2082607788 abstract "Natural killer (NK) cells function through a diverse array of cell-surface natural killer receptors (NCRs). NCRs specific for classical and non-classical MHC class I proteins, expressed in complex patterns of inhibitory and activating isoforms on overlapping, but distinct, subsets of NK cells, play an important role in immunosurveillance against cells that have reduced MHC class I expression as a result of infection or transformation. Another NCR, NKG2D, is an activating NCR first identified on NK cells, but subsequently found on macrophages and a variety of T cell types. NKG2D ligands in rodents include the MHC class I-like proteins RAE-1 and H60 and, in humans, ULBPs and the cell stress-inducible proteins MICA and MICB. NKG2D–MIC and –RAE-1 recognition events have been implicated in anti-viral and -tumor immune responses. Crystallographic analyses of NKG2D–MICA and –RAE-1 complexes reveal an unusual mode of recognition that apparently tolerates a surprising degree of ligand plasticity while generating affinities that are among the strongest TCR– or NCR–ligand affinities, thus, far described." @default.
• W2082607788 created "2016-06-24" @default.
• W2082607788 creator A5030551505 @default.
• W2082607788 date "2002-05-01" @default.
• W2082607788 modified "2023-10-02" @default.
• W2082607788 title "Asymmetric ligand recognition by the activating natural killer cell receptor NKG2D, a symmetric homodimer" @default.
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• W2082607788 doi "https://doi.org/10.1016/s0161-5890(02)00032-9" @default.
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