7TVB
Stat5A Core in Complex with AK305
Summary for 7TVB
Entry DOI | 10.2210/pdb7tvb/pdb |
Descriptor | 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) |
Functional Keywords | stat5a, activator, transcription |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 66788.74 |
Authors | Meagher, J.L.,Stuckey, J.A. (deposition date: 2022-02-04, release date: 2023-02-15, Last modification date: 2024-04-03) |
Primary citation | 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 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.653 Å) |
Structure validation
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