7TVB
Stat5A Core in Complex with AK305
7TVB の概要
| エントリーDOI | 10.2210/pdb7tvb/pdb |
| 分子名称 | Signal transducer and activator of transcription 5A, N-{5-[difluoro(phosphono)methyl]-1-benzothiophene-2-carbonyl}-3-methyl-L-valyl-L-prolyl-N,N-dimethyl-N~3~-[4-(1,3-thiazol-2-yl)phenyl]-beta-alaninamide, GLYCEROL, ... (4 entities in total) |
| 機能のキーワード | stat5a, activator, transcription |
| 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 | 66788.74 |
| 構造登録者 | |
| 主引用文献 | Kaneshige, A.,Bai, L.,Wang, M.,McEachern, D.,Meagher, J.L.,Xu, R.,Wang, Y.,Jiang, W.,Metwally, H.,Kirchhoff, P.D.,Zhao, L.,Jiang, H.,Wang, M.,Wen, B.,Sun, D.,Stuckey, J.A.,Wang, S. A selective small-molecule STAT5 PROTAC degrader capable of achieving tumor regression in vivo. Nat.Chem.Biol., 19:703-711, 2023 Cited by PubMed Abstract: Signal transducer and activator of transcription 5 (STAT5) is an attractive therapeutic target, but successful targeting of STAT5 has proved to be difficult. Here we report the development of AK-2292 as a first, potent and selective small-molecule degrader of both STAT5A and STAT5B isoforms. AK-2292 induces degradation of STAT5A/B proteins with an outstanding selectivity over all other STAT proteins and more than 6,000 non-STAT proteins, leading to selective inhibition of STAT5 activity in cells. AK-2292 effectively induces STAT5 depletion in normal mouse tissues and human chronic myeloid leukemia (CML) xenograft tissues and achieves tumor regression in two CML xenograft mouse models at well-tolerated dose schedules. AK-2292 is not only a powerful research tool with which to investigate the biology of STAT5 and the therapeutic potential of selective STAT5 protein depletion and inhibition but also a promising lead compound toward ultimate development of a STAT5-targeted therapy. PubMed: 36732620DOI: 10.1038/s41589-022-01248-4 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.653 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






