6SO4

Fragment RZ132 in complex with MAP kinase p38-alpha

6SO4 の概要

• エントリーDOI: 10.2210/pdb6so4/pdb
• 分子名称: Mitogen-activated protein kinase 14, (2~{S})-2-methyl-4-(oxetan-3-yl)-~{N}-(phenylmethyl)piperazine-2-carboxamide, CHLORIDE ION, ... (6 entities in total)
• 機能のキーワード: fbdd, fragment based drug design, p38, mapk14, kinase, transferase., transferase
• 由来する生物種: Mus musculus (House mouse)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 44527.26

構造登録者

Nichols, C.E.,De Nicola, G.F. (登録日: 2019-08-29, 公開日: 2019-09-11, 最終更新日: 2024-01-24)

主引用文献

Nichols, C.,Ng, J.,Keshu, A.,Kelly, G.,Conte, M.R.,Marber, M.S.,Fraternali, F.,De Nicola, G.F.
Mining the PDB for Tractable Cases Where X-ray Crystallography Combined with Fragment Screens Can Be Used to Systematically Design Protein-Protein Inhibitors: Two Test Cases Illustrated by IL1 beta-IL1R and p38 alpha-TAB1 Complexes.
J.Med.Chem., 63:7559-7568, 2020

PubMed Abstract: Nowadays, it is possible to combine X-ray crystallography and fragment screening in a medium throughput fashion to chemically probe the surfaces used by proteins to interact and use the outcome of the screens to systematically design protein-protein inhibitors. To prove it, we first performed a bioinformatics analysis of the Protein Data Bank protein complexes, which revealed over 400 cases where the crystal lattice of the target in the free form is such that large portions of the interacting surfaces are free from lattice contacts and therefore accessible to fragments during soaks. Among the tractable complexes identified, we then performed single fragment crystal screens on two particular interesting cases: the Il1β-ILR and p38α-TAB1 complexes. The result of the screens showed that fragments tend to bind in clusters, highlighting the small-molecule hotspots on the surface of the target protein. In most of the cases, the hotspots overlapped with the binding sites of the interacting proteins.

PubMed: 32543856
DOI: 10.1021/acs.jmedchem.0c00403

実験手法

X-RAY DIFFRACTION (1.51 Å)