3I6K
Newly identified epitope from SARS-CoV membrane protein complexed with HLA-A*0201
3I6K の概要
エントリーDOI | 10.2210/pdb3i6k/pdb |
分子名称 | HLA class I histocompatibility antigen, A-2 alpha chain, Beta-2-microglobulin, Membrane glycoprotein peptide, ... (4 entities in total) |
機能のキーワード | hla-a2, sars-cov, membrane glycoprotein, disulfide bond, glycoprotein, host-virus interaction, immune response, membrane, mhc i, phosphoprotein, transmembrane, disease mutation, glycation, immunoglobulin domain, pyrrolidone carboxylic acid, secreted, envelope protein, golgi apparatus, viral matrix protein, virion, immune system |
由来する生物種 | Homo sapiens (human) 詳細 |
細胞内の位置 | Membrane; Single-pass type I membrane protein: P01892 Secreted: P61769 |
タンパク質・核酸の鎖数 | 6 |
化学式量合計 | 89481.61 |
構造登録者 | |
主引用文献 | Liu, J.,Sun, Y.,Qi, J.,Chu, F.,Wu, H.,Gao, F.,Li, T.,Yan, J.,Gao, G.F. The membrane protein of severe acute respiratory syndrome coronavirus acts as a dominant immunogen revealed by a clustering region of novel functionally and structurally defined cytotoxic T-lymphocyte epitopes J Infect Dis, 202:1171-1180, 2010 Cited by PubMed Abstract: Severe acute respiratory syndrome coronavirus (SARS-CoV), which emerged with highly contagious and life-threatening characteristics in 2002, remains a potential risk for future outbreaks. Membrane (M) and envelope (E) proteins are major structural proteins of the SARS-CoV. The M protein has been determined as a protective antigen in humoral responses. However, its potential roles in stimulating cellular immunity remain elusive. PubMed: 20831383DOI: 10.1086/656315 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.8 Å) |
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