3VPP
Crystal Structure of the Human CLEC9A C-type Lectin-Like Domain
3VPP の概要
| エントリーDOI | 10.2210/pdb3vpp/pdb |
| 分子名称 | C-type lectin domain family 9 member A, CALCIUM ION (3 entities in total) |
| 機能のキーワード | dendritic cell, c-type lectin-like domain, membrane, immune system |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Membrane; Single-pass type II membrane protein: Q6UXN8 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 30199.51 |
| 構造登録者 | Czabotar, P.E.,Zhang, J.G.,Policheni, A.N.,Shortman, K.,Lahoud, M.H.,Colman, P.M. (登録日: 2012-03-07, 公開日: 2012-04-25, 最終更新日: 2024-10-30) |
| 主引用文献 | Zhang, J.G.,Czabotar, P.E.,Policheni, A.N.,Caminschi, I.,Wan, S.S.,Kitsoulis, S.,Tullett, K.M.,Robin, A.Y.,Brammananth, R.,van Delft, M.F.,Lu, J.,O'Reilly, L.A.,Josefsson, E.C.,Kile, B.T.,Chin, W.J.,Mintern, J.D.,Olshina, M.A.,Wong, W.,Baum, J.,Wright, M.D.,Huang, D.C.,Mohandas, N.,Coppel, R.L.,Colman, P.M.,Nicola, N.A.,Shortman, K.,Lahoud, M.H. The dendritic cell receptor Clec9A binds damaged cells via exposed actin filaments. Immunity, 36:646-657, 2012 Cited by PubMed Abstract: The immune system must distinguish viable cells from cells damaged by physical and infective processes. The damaged cell-recognition molecule Clec9A is expressed on the surface of the mouse and human dendritic cell subsets specialized for the uptake and processing of material from dead cells. Clec9A recognizes a conserved component within nucleated and nonnucleated cells, exposed when cell membranes are damaged. We have identified this Clec9A ligand as a filamentous form of actin in association with particular actin-binding domains of cytoskeletal proteins. We have determined the crystal structure of the human CLEC9A C-type lectin domain and propose a functional dimeric structure with conserved tryptophans in the ligand recognition site. Mutation of these residues ablated CLEC9A binding to damaged cells and to the isolated ligand complexes. We propose that Clec9A provides targeted recruitment of the adaptive immune system during infection and can also be utilized to enhance immune responses generated by vaccines. PubMed: 22483802DOI: 10.1016/j.immuni.2012.03.009 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.642 Å) |
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