5MQE
Crystal structure of CREBBP bromodomain complexed with CBP006
5MQE の概要
エントリーDOI | 10.2210/pdb5mqe/pdb |
分子名称 | CREB-binding protein, 4-bromanyl-~{N}-methyl-1~{H}-pyrrole-2-carboxamide (3 entities in total) |
機能のキーワード | crebbp bromodomain, inhibitor, transcription |
由来する生物種 | Homo sapiens (Human) |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 28852.77 |
構造登録者 | |
主引用文献 | Spiliotopoulos, D.,Zhu, J.,Wamhoff, E.C.,Deerain, N.,Marchand, J.R.,Aretz, J.,Rademacher, C.,Caflisch, A. Virtual screen to NMR (VS2NMR): Discovery of fragment hits for the CBP bromodomain. Bioorg. Med. Chem. Lett., 27:2472-2478, 2017 Cited by PubMed Abstract: Overexpression of the CREB-binding protein (CBP), a bromodomain-containing transcription coactivator involved in a variety of cellular processes, has been observed in several types of cancer with a correlation to aggressiveness. We have screened a library of nearly 1500 fragments by high-throughput docking into the CBP bromodomain followed by binding energy evaluation using a force field with electrostatic solvation. Twenty of the 39 fragments selected by virtual screening are positive in one or more ligand-observed nuclear magnetic resonance (NMR) experiments. Four crystal structures of the CBP bromodomain in complex with in silico screening hits validate the pose predicted by docking. Thus, the success ratio of the high-throughput docking procedure is 50% or 10% if one considers the validation by ligand-observed NMR spectroscopy or X-ray crystallography, respectively. Compounds 1 and 3 show favorable ligand efficiency in two different in vitro binding assays. The structure of the CBP bromodomain in the complex with the brominated pyrrole 1 suggests fragment growing by Suzuki coupling. PubMed: 28410781DOI: 10.1016/j.bmcl.2017.04.001 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.65 Å) |
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