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6. Crystal structures of murine MHC Class I H-2 D(b) and K(b) molecules in complex with CTL epitopes from influenza A virus: implications for TCR repertoire selection and immunodominance. Meijers R; Lai CC; Yang Y; Liu JH; Zhong W; Wang JH; Reinherz EL J Mol Biol; 2005 Feb; 345(5):1099-110. PubMed ID: 15644207 [TBL] [Abstract][Full Text] [Related]
7. Recognition of an MHC class I-restricted antigenic peptide can be modulated by para-substitution of its buried tyrosine residues in a TCR-specific manner. Saito NG; Chang HC; Paterson Y J Immunol; 1999 May; 162(10):5998-6008. PubMed ID: 10229839 [TBL] [Abstract][Full Text] [Related]
8. The signal sequence of lymphocytic choriomeningitis virus contains an immunodominant cytotoxic T cell epitope that is restricted by both H-2D(b) and H-2K(b) molecules. Hudrisier D; Oldstone MB; Gairin JE Virology; 1997 Jul; 234(1):62-73. PubMed ID: 9234947 [TBL] [Abstract][Full Text] [Related]
9. Modeling the interactions of a peptide-major histocompatibility class I ligand with its receptors. II. Cross-reaction between a monoclonal antibody and two alpha beta T cell receptors. Rognan D; Engberg J; Stryhn A; Andersen PS; Buus S J Comput Aided Mol Des; 2000 Jan; 14(1):71-82. PubMed ID: 10702926 [TBL] [Abstract][Full Text] [Related]
10. The critical role of a solvent-exposed residue of an MHC class I-restricted peptide in MHC-peptide binding. Huard R; Dyall R; Nikolić-Zugić J Int Immunol; 1997 Nov; 9(11):1701-7. PubMed ID: 9418131 [TBL] [Abstract][Full Text] [Related]
11. Recognition of the Major Histocompatibility Complex (MHC) Class Ib Molecule H2-Q10 by the Natural Killer Cell Receptor Ly49C. Sullivan LC; Berry R; Sosnin N; Widjaja JM; Deuss FA; Balaji GR; LaGruta NL; Mirams M; Trapani JA; Rossjohn J; Brooks AG; Andrews DM J Biol Chem; 2016 Sep; 291(36):18740-52. PubMed ID: 27385590 [TBL] [Abstract][Full Text] [Related]
12. Crystal structure of an H-2Kb-ovalbumin peptide complex reveals the interplay of primary and secondary anchor positions in the major histocompatibility complex binding groove. Fremont DH; Stura EA; Matsumura M; Peterson PA; Wilson IA Proc Natl Acad Sci U S A; 1995 Mar; 92(7):2479-83. PubMed ID: 7708669 [TBL] [Abstract][Full Text] [Related]
13. Structural basis for the restoration of TCR recognition of an MHC allelic variant by peptide secondary anchor substitution. Miley MJ; Messaoudi I; Metzner BM; Wu Y; Nikolich-Zugich J; Fremont DH J Exp Med; 2004 Dec; 200(11):1445-54. PubMed ID: 15557346 [TBL] [Abstract][Full Text] [Related]
14. The NK cell MHC class I receptor Ly49A detects mutations on H-2Dd inside and outside of the peptide binding groove. Matsumoto N; Yokoyama WM; Kojima S; Yamamoto K J Immunol; 2001 Apr; 166(7):4422-8. PubMed ID: 11254697 [TBL] [Abstract][Full Text] [Related]
15. Three-dimensional structure of H-2Dd complexed with an immunodominant peptide from human immunodeficiency virus envelope glycoprotein 120. Li H; Natarajan K; Malchiodi EL; Margulies DH; Mariuzza RA J Mol Biol; 1998; 283(1):179-91. PubMed ID: 9761682 [TBL] [Abstract][Full Text] [Related]
16. Immunobiological analysis of TCR single-chain transgenic mice reveals new possibilities for interaction between CDR3alpha and an antigenic peptide bound to MHC class I. Zhang W; Honda S; Wang F; DiLorenzo TP; Kalergis AM; Ostrov DA; Nathenson SG J Immunol; 2001 Oct; 167(8):4396-404. PubMed ID: 11591764 [TBL] [Abstract][Full Text] [Related]
17. Presentation of a self-peptide for in vivo tolerance induction of CD4+ T cells is governed by a processing factor that maps to the class II region of the major histocompatibility complex locus. Fedoseyeva EV; Tam RC; Orr PL; Garovoy MR; Benichou G J Exp Med; 1995 Nov; 182(5):1481-91. PubMed ID: 7595218 [TBL] [Abstract][Full Text] [Related]
18. Emerging principles for the recognition of peptide antigens by MHC class I molecules. Matsumura M; Fremont DH; Peterson PA; Wilson IA Science; 1992 Aug; 257(5072):927-34. PubMed ID: 1323878 [TBL] [Abstract][Full Text] [Related]
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