4GMB
Crystal structure of human WD repeat domain 5 with compound MM-402
4GMB の概要
| エントリーDOI | 10.2210/pdb4gmb/pdb |
| 関連するPDBエントリー | 4GM3 4GM8 4GM9 |
| 関連するBIRD辞書のPRD_ID | PRD_000896 |
| 分子名称 | WD repeat-containing protein 5, MM-402 (3 entities in total) |
| 機能のキーワード | mll1, histone methyltransferase, wd40, transcription-transcription inhibitor complex, transcription/transcription inhibitor |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Nucleus : P61964 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 35024.79 |
| 構造登録者 | Karatas, H.,Townsend, E.C.,Chen, Y.,Bernard, D.,Cao, F.,Liu, L.,Lei, M.,Dou, Y.,Wang, S. (登録日: 2012-08-15, 公開日: 2014-02-19, 最終更新日: 2023-11-15) |
| 主引用文献 | Karatas, H.,Li, Y.,Liu, L.,Ji, J.,Lee, S.,Chen, Y.,Yang, J.,Huang, L.,Bernard, D.,Xu, J.,Townsend, E.C.,Cao, F.,Ran, X.,Li, X.,Wen, B.,Sun, D.,Stuckey, J.A.,Lei, M.,Dou, Y.,Wang, S. Discovery of a Highly Potent, Cell-Permeable Macrocyclic Peptidomimetic (MM-589) Targeting the WD Repeat Domain 5 Protein (WDR5)-Mixed Lineage Leukemia (MLL) Protein-Protein Interaction. J.Med.Chem., 60:4818-4839, 2017 Cited by PubMed Abstract: We report herein the design, synthesis, and evaluation of macrocyclic peptidomimetics that bind to WD repeat domain 5 (WDR5) and block the WDR5-mixed lineage leukemia (MLL) protein-protein interaction. Compound 18 (MM-589) binds to WDR5 with an IC value of 0.90 nM (K value <1 nM) and inhibits the MLL H3K4 methyltransferase (HMT) activity with an IC value of 12.7 nM. Compound 18 potently and selectively inhibits cell growth in human leukemia cell lines harboring MLL translocations and is >40 times better than the previously reported compound MM-401. Cocrystal structures of 16 and 18 complexed with WDR5 provide structural basis for their high affinity binding to WDR5. Additionally, we have developed and optimized a new AlphaLISA-based MLL HMT functional assay to facilitate the functional evaluation of these designed compounds. Compound 18 represents the most potent inhibitor of the WDR5-MLL interaction reported to date, and further optimization of 18 may yield a new therapy for acute leukemia. PubMed: 28603984DOI: 10.1021/acs.jmedchem.6b01796 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.781 Å) |
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