7SS8
Human P300 complexed with a proline-based inhibitor
7SS8 の概要
| エントリーDOI | 10.2210/pdb7ss8/pdb |
| 分子名称 | Histone acetyltransferase p300, ZINC ION, 1,2-ETHANEDIOL, ... (5 entities in total) |
| 機能のキーワード | histone acetyltransferase, transferase, transferase-inhibitor complex, transferase/inhibitor |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 66916.32 |
| 構造登録者 | |
| 主引用文献 | Tian, X.,Suarez, D.,Thomson, D.,Li, W.,King, E.A.,LaFrance, L.,Boehm, J.,Barton, L.,Di Marco, C.,Martyr, C.,Thalji, R.,Medina, J.,Knight, S.,Heerding, D.,Gao, E.,Nartey, E.,Cecconie, T.,Nixon, C.,Zhang, G.,Berrodin, T.J.,Phelps, C.,Patel, A.,Bai, X.,Lind, K.,Prabhu, N.,Messer, J.,Zhu, Z.,Shewchuk, L.,Reid, R.,Graves, A.P.,McHugh, C.,Mangatt, B. Discovery of Proline-Based p300/CBP Inhibitors Using DNA-Encoded Library Technology in Combination with High-Throughput Screening. J.Med.Chem., 65:14391-14408, 2022 Cited by PubMed Abstract: E1A binding protein (p300) and CREB binding protein (CBP) are two highly homologous and multidomain histone acetyltransferases. These two proteins are involved in many cellular processes by acting as coactivators of a large number of transcription factors. Dysregulation of p300/CBP has been found in a variety of cancers and other diseases, and inhibition has been shown to decrease Myc expression. Herein, we report the identification of a series of highly potent, proline-based small-molecule p300/CBP histone acetyltransferase (HAT) inhibitors using DNA-encoded library technology in combination with high-throughput screening. The strategy of reducing ChromlogD and fluorination of metabolic soft spots was explored to improve the pharmacokinetic properties of potent p300 inhibitors. Fluorination of both cyclobutyl and proline rings of led to not only reduced clearance but also improved cMyc cellular potency. PubMed: 36302181DOI: 10.1021/acs.jmedchem.2c00670 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.15 Å) |
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