504 related articles for article (PubMed ID: 17024283)
1. Synthesis and biological evaluation of two chemically modified peptide epitopes for the class I MHC protein HLA-B*2705.
Jones MA; Hislop AD; Snaith JS
Org Biomol Chem; 2006 Oct; 4(20):3769-77. PubMed ID: 17024283
[TBL] [Abstract][Full Text] [Related]
2. T cell receptor recognition of a 'super-bulged' major histocompatibility complex class I-bound peptide.
Tynan FE; Burrows SR; Buckle AM; Clements CS; Borg NA; Miles JJ; Beddoe T; Whisstock JC; Wilce MC; Silins SL; Burrows JM; Kjer-Nielsen L; Kostenko L; Purcell AW; McCluskey J; Rossjohn J
Nat Immunol; 2005 Nov; 6(11):1114-22. PubMed ID: 16186824
[TBL] [Abstract][Full Text] [Related]
3. Alloreactive T cell recognition of MHC class I molecules: the T cell receptor interacts with limited regions of the MHC class I long alpha helices.
Smith KD; Lutz CT
J Immunol; 1997 Mar; 158(6):2805-12. PubMed ID: 9058816
[TBL] [Abstract][Full Text] [Related]
4. NK cell recognition of MHC class I. NK cells are sensitive to peptide-binding groove and surface alpha-helical mutations that affect T cells.
Kurago ZB; Smith KD; Lutz CT
J Immunol; 1995 Mar; 154(6):2631-41. PubMed ID: 7876538
[TBL] [Abstract][Full Text] [Related]
5. Nonapeptide analogues containing (R)-3-hydroxybutanoate and beta-homoalanine oligomers: synthesis and binding affinity to a class I major histocompatibility complex protein.
Poenaru S; Lamas JR; Folkers G; López de Castro JA; Seebach D; Rognan D
J Med Chem; 1999 Jul; 42(13):2318-31. PubMed ID: 10395472
[TBL] [Abstract][Full Text] [Related]
6. The impact of HLA-B micropolymorphism outside primary peptide anchor pockets on the CTL response to CMV.
Burrows JM; Wynn KK; Tynan FE; Archbold J; Miles JJ; Bell MJ; Brennan RM; Walker S; McCluskey J; Rossjohn J; Khanna R; Burrows SR
Eur J Immunol; 2007 Apr; 37(4):946-53. PubMed ID: 17357107
[TBL] [Abstract][Full Text] [Related]
7. In vitro mutagenesis of HLA-B27. Amino acid substitutions at position 67 disrupt anti-B27 monoclonal antibody binding in direct relation to the size of the substituted side chain.
el-Zaatari FA; Sams KC; Taurog JD
J Immunol; 1990 Feb; 144(4):1512-7. PubMed ID: 1689355
[TBL] [Abstract][Full Text] [Related]
8. A pattern search method for putative anchor residues in T cell epitopes.
Hobohm U; Meyerhans A
Eur J Immunol; 1993 Jun; 23(6):1271-6. PubMed ID: 7684684
[TBL] [Abstract][Full Text] [Related]
9. Extended repertoire of permissible peptide ligands for HLA-B*2702.
Raghavan M; Lebrón JA; Johnson JL; Bjorkman PJ
Protein Sci; 1996 Oct; 5(10):2080-8. PubMed ID: 8897608
[TBL] [Abstract][Full Text] [Related]
10. Changes at the floor of the peptide-binding groove induce a strong preference for proline at position 3 of the bound peptide: molecular dynamics simulations of HLA-A*0217.
Toh H; Savoie CJ; Kamikawaji N; Muta S; Sasazuki T; Kuhara S
Biopolymers; 2000 Oct; 54(5):318-27. PubMed ID: 10935972
[TBL] [Abstract][Full Text] [Related]
11. Unusual topology of an HLA-B27 allospecific T cell epitope lacking peptide specificity.
Villadangos JA; Galocha B; López de Castro JA
J Immunol; 1994 Mar; 152(5):2317-23. PubMed ID: 7510742
[TBL] [Abstract][Full Text] [Related]
12. Immunogenicity of peptides bound to MHC class I molecules depends on the MHC-peptide complex stability.
van der Burg SH; Visseren MJ; Brandt RM; Kast WM; Melief CJ
J Immunol; 1996 May; 156(9):3308-14. PubMed ID: 8617954
[TBL] [Abstract][Full Text] [Related]
13. The peptide length specificity of some HLA class I alleles is very broad and includes peptides of up to 25 amino acids in length.
Bell MJ; Burrows JM; Brennan R; Miles JJ; Tellam J; McCluskey J; Rossjohn J; Khanna R; Burrows SR
Mol Immunol; 2009 May; 46(8-9):1911-7. PubMed ID: 19157553
[TBL] [Abstract][Full Text] [Related]
14. Characterization of peptide binding to the murine MHC class I H-2Kk molecule. Sequencing of the bound peptides and direct binding of synthetic peptides to isolated class I molecules.
Brown EL; Wooters JL; Ferenz CR; O'Brien CM; Hewick RM; Herrmann SH
J Immunol; 1994 Oct; 153(7):3079-92. PubMed ID: 7522249
[TBL] [Abstract][Full Text] [Related]
15. Peptide selection by MHC class I molecules.
Schumacher TN; De Bruijn ML; Vernie LN; Kast WM; Melief CJ; Neefjes JJ; Ploegh HL
Nature; 1991 Apr; 350(6320):703-6. PubMed ID: 1708852
[TBL] [Abstract][Full Text] [Related]
16. Impact of MHC class I alleles on the M. tuberculosis antigen-specific CD8+ T-cell response in patients with pulmonary tuberculosis.
Weichold FF; Mueller S; Kortsik C; Hitzler WE; Wulf MJ; Hone DM; Sadoff JC; Maeurer MJ
Genes Immun; 2007 Jun; 8(4):334-43. PubMed ID: 17429413
[TBL] [Abstract][Full Text] [Related]
17. Anti-HLA-E mAb 3D12 mimics MEM-E/02 in binding to HLA-B and HLA-C alleles: Web-tools validate the immunogenic epitopes of HLA-E recognized by the antibodies.
Ravindranath MH; Pham T; El-Awar N; Kaneku H; Terasaki PI
Mol Immunol; 2011 Jan; 48(4):423-30. PubMed ID: 21145594
[TBL] [Abstract][Full Text] [Related]
18. Overlapping peptide-binding specificities of HLA-B27 and B39: evidence for a role of peptide supermotif in the pathogenesis of spondylarthropathies.
Sobao Y; Tsuchiya N; Takiguchi M; Tokunaga K
Arthritis Rheum; 1999 Jan; 42(1):175-81. PubMed ID: 9920028
[TBL] [Abstract][Full Text] [Related]
19. T cell recognition of MHC class II-associated peptides is independent of peptide affinity for MHC and sodium dodecyl sulfate stability of the peptide/MHC complex. Effects of conservative amino acid substitutions at anchor position 1 of influenza matrix protein19-31.
Wu S; Gorski J; Eckels DD; Newton-Nash DK
J Immunol; 1996 May; 156(10):3815-20. PubMed ID: 8621918
[TBL] [Abstract][Full Text] [Related]
20. Conformational and structural characteristics of peptides binding to HLA-DR molecules.
Hill CM; Hayball JD; Allison AA; Rothbard JB
J Immunol; 1991 Jul; 147(1):189-97. PubMed ID: 1711073
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]