6CQF
Crystal structure of HPK1 in complex an inhibitor G1858
6CQF の概要
| エントリーDOI | 10.2210/pdb6cqf/pdb |
| 分子名称 | Mitogen-activated protein kinase kinase kinase kinase 1, N-{2-(3,3-difluoropyrrolidin-1-yl)-6-[(3R)-pyrrolidin-3-yl]pyrimidin-4-yl}-1-(propan-2-yl)-1H-pyrazolo[4,3-c]pyridin-6-amine (3 entities in total) |
| 機能のキーワード | protein kinase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
| 由来する生物種 | Homo sapiens (Human) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 33548.89 |
| 構造登録者 | Wu, P.,Lehoux, I.,Mortara, K.,Franke, Y.,Chan, B.K.,Wang, W. (登録日: 2018-03-15, 公開日: 2018-12-19, 最終更新日: 2024-03-13) |
| 主引用文献 | Wu, P.,Sneeringer, C.J.,Pitts, K.E.,Day, E.S.,Chan, B.K.,Wei, B.,Lehoux, I.,Mortara, K.,Li, H.,Wu, J.,Franke, Y.,Moffat, J.G.,Grogan, J.L.,Heffron, T.P.,Wang, W. Hematopoietic Progenitor Kinase-1 Structure in a Domain-Swapped Dimer. Structure, 27:125-133.e4, 2019 Cited by PubMed Abstract: Enhancement of antigen-specific T cell immunity has shown significant therapeutic benefit in infectious diseases and cancer. Hematopoietic progenitor kinase-1 (HPK1) is a negative-feedback regulator of T cell receptor signaling, which dampens T cell proliferation and effector function. A recent report showed that a catalytic dead mutant of HPK1 phenocopies augmented T cell responses observed in HPK1-knockout mice, indicating that kinase activity is critical for function. We evaluated active and inactive mutants and determined crystal structures of HPK1 kinase domain (HPK1-KD) in apo and ligand bound forms. In all structures HPK1-KD displays a rare domain-swapped dimer, in which the activation segment comprises a well-conserved dimer interface. Biophysical measurements show formation of dimer in solution. The activation segment adopts an α-helical structure which exhibits distinct orientations in active and inactive states. This face-to-face configuration suggests that the domain-swapped dimer may possess alternative selectivity for certain substrates of HPK1 under relevant cellular context. PubMed: 30503777DOI: 10.1016/j.str.2018.10.025 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.246 Å) |
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