A Structural Basis for the Selection of Dominant αβ T Cell Receptors in Antiviral Immunity
Top Cited Papers
- 31 January 2003
- Vol. 18 (1) , 53-64
- https://doi.org/10.1016/s1074-7613(02)00513-7
Abstract
No abstract availableKeywords
This publication has 52 references indexed in Scilit:
- Crystal structure of a T cell receptor Vα11 (AV11S5) domain: new canonical forms for the first and second complementarity determining regionsJournal of Molecular Biology, 2001
- Canonical structures for the hypervariable regions of T cell αβ receptorsJournal of Molecular Biology, 2000
- One of the CD3ε Subunits within a T Cell Receptor Complex Lies in Close Proximity to the Cβ FG LoopThe Journal of Experimental Medicine, 1998
- Identification of a common docking topology with substantial variation among different TCR–peptide–MHC complexesCurrent Biology, 1998
- Cross‐reactive memory T cells for Epstein‐Barr virus augment the alloresponse to common human leukocyte antigens: degenerate recognition of major histocompatibility complex‐bound peptide by T cells and its role in alloreactivityEuropean Journal of Immunology, 1997
- Human leukocyte antigen phenotype imposes complex constraints on the antigen‐specific cytotoxic T lymphocyte repertoireEuropean Journal of Immunology, 1997
- An alloresponse in humans is dominated by cytotoxic T lymphocytes (CTL) cross-reactive with a single Epstein-Barr virus CTL epitope: implications for graft-versus-host disease.The Journal of Experimental Medicine, 1994
- Shape Complementarity at Protein/Protein InterfacesJournal of Molecular Biology, 1993
- T-cell antigen receptor genes and T-cell recognitionNature, 1988
- Canonical structures for the hypervariable regions of immunoglobulinsJournal of Molecular Biology, 1987