4GAW
Crystal structure of active human granzyme H
4GAW の概要
| エントリーDOI | 10.2210/pdb4gaw/pdb |
| 関連するPDBエントリー | 4GA7 |
| 分子名称 | Granzyme H, SULFATE ION, CHLORIDE ION, ... (4 entities in total) |
| 機能のキーワード | serine protease, cytolysis, hydrolase, cytotoxic granules |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Cytoplasmic granule: P20718 |
| タンパク質・核酸の鎖数 | 12 |
| 化学式量合計 | 304096.30 |
| 構造登録者 | |
| 主引用文献 | Wang, L.,Li, Q.,Wu, L.,Liu, S.,Zhang, Y.,Yang, X.,Zhu, P.,Zhang, H.,Zhang, K.,Lou, J.,Liu, P.,Tong, L.,Sun, F.,Fan, Z. Identification of SERPINB1 as a physiological inhibitor of human granzyme H J.Immunol., 190:1319-1330, 2013 Cited by PubMed Abstract: The granzyme/perforin pathway is a major mechanism for cytotoxic lymphocytes to eliminate virus-infected and tumor cells. The balance between activation and inhibition of the proteolytic cascade must be tightly controlled to avoid self damage. Granzyme H (GzmH) is constitutively expressed in NK cells and induces target cell death; however, how GzmH activity is regulated remains elusive. We reported earlier the crystal structures of inactive D102N-GzmH alone and in complex with its synthetic substrate and inhibitor, as well as defined the mechanisms of substrate recognition and enzymatic activation. In this study, we identified SERPINB1 as a potent intracellular inhibitor for GzmH. Upon cleavage of the reactive center loop at Phe(343), SERPINB1 forms an SDS-stable covalent complex with GzmH. SERPINB1 overexpression suppresses GzmH- or LAK cell-mediated cytotoxicity. We determined the crystal structures of active GzmH and SERPINB1 (LM-DD mutant) in the native conformation to 3.0- and 2.9-Å resolution, respectively. Molecular modeling reveals the possible conformational changes in GzmH for the suicide inhibition. Our findings provide new insights into the inhibitory mechanism of SERPINB1 against human GzmH. PubMed: 23269243DOI: 10.4049/jimmunol.1202542 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (3 Å) |
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