1FNE
HISTOCOMPATIBILITY ANTIGEN
1FNE の概要
エントリーDOI | 10.2210/pdb1fne/pdb |
関連するPDBエントリー | 1iea |
分子名称 | PROTEIN (MHC CLASS II I-EK, ALPHA CHAIN), PROTEIN (MHC CLASS II I-EK, BETA CHAIN), 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total) |
機能のキーワード | histocompatibility antigen, mhc, immune system |
由来する生物種 | Mus musculus (house mouse) 詳細 |
細胞内の位置 | Membrane ; Single-pass type I membrane protein : P04224 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 96773.86 |
構造登録者 | |
主引用文献 | Kersh, G.J.,Miley, M.J.,Nelson, C.A.,Grakoui, A.,Horvath, S.,Donermeyer, D.L.,Kappler, J.,Allen, P.M.,Fremont, D.H. Structural and functional consequences of altering a peptide MHC anchor residue. J.Immunol., 166:3345-3354, 2001 Cited by PubMed Abstract: To better understand TCR discrimination of multiple ligands, we have analyzed the crystal structures of two Hb peptide/I-E(k) complexes that differ by only a single amino acid substitution at the P6 anchor position within the peptide (E73D). Detailed comparison of multiple independently determined structures at 1.9 A resolution reveals that removal of a single buried methylene group can alter a critical portion of the TCR recognition surface. Significant variance was observed in the peptide P5-P8 main chain as well as a rotamer difference at LeuP8, approximately 10 A distal from the substitution. No significant variations were observed in the conformation of the two MHC class II molecules. The ligand alteration results in two peptide/MHC complexes that generate bulk T cell responses that are distinct and essentially nonoverlapping. For the Hb-specific T cell 3.L2, substitution reduces the potency of the ligand 1000-fold. Soluble 3.L2 TCR binds the two peptide/MHC complexes with similar affinity, although with faster kinetics. These results highlight the role of subtle variations in MHC Ag presentation on T cell activation and signaling. PubMed: 11207290主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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