3I6G
Newly identified epitope Mn2 from SARS-CoV M protein complexed withHLA-A*0201
Summary for 3I6G
Entry DOI | 10.2210/pdb3i6g/pdb |
Descriptor | HLA class I histocompatibility antigen, A-2 alpha chain, Beta-2-microglobulin, Membrane protein, ... (4 entities in total) |
Functional Keywords | 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 |
Biological source | Homo sapiens (human) More |
Cellular location | Membrane; Single-pass type I membrane protein: P01892 Secreted: P61769 Virion membrane; Multi-pass membrane protein (Potential): P59596 |
Total number of polymer chains | 6 |
Total formula weight | 89697.81 |
Authors | |
Primary citation | 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: 20831383DOI: 10.1086/656315 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.201 Å) |
Structure validation
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