8HKO

Mutated human ADP-ribosyltransferase 2 (PARP2) catalytic domain bound to Rucaparib

8HKO の概要

• エントリーDOI: 10.2210/pdb8hko/pdb
• 分子名称: Poly [ADP-ribose] polymerase 2, GLYCEROL, Rucaparib, ... (4 entities in total)
• 機能のキーワード: dna adp-ribosyltransferase 2, parp2, rucaparib, transferase
• 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: 81131.11

構造登録者

Wang, X.Y.,Zhou, J.,Xu, B.L. (登録日: 2022-11-27, 公開日: 2024-05-01, 最終更新日: 2025-05-14)

主引用文献

Wang, X.,Zhou, J.,Xu, B.
Engaging an engineered PARP-2 catalytic domain mutant to solve the complex structures harboring approved drugs for structure analyses.
Bioorg.Chem., 160:108471-108471, 2025

PubMed Abstract: The PARP-1/2 inhibitors have been approved for the treatment of cancers by modulating the enzymatic activity and/or the trapping ability for damaged DNA of PARP-1 and/or PARP-2, and the selective PARP-1 inhibitors are now attracting considerable attention with an aim to search for drug candidates with an improved safety. Exploring the structural basis of the selectivity and trapping capability of known PARP-1/2 inhibitors would be beneficial for the discovery of the improved inhibitors. Herein, a mutated PARP-2 catalytic domain, designated as catPARP-2SE, was engineered. It could be expressed in an elevated level and had capability to crystalize at 25 °C, which greatly facilitated obtaining PARP-2 crystals. Consequently, the complex structures of Fluzoparib, Pamiparib, Rucaparib, and Niraparib within PARP-2 were achieved. Taking advantage of these complexed structures, the detailed and quantitative analyses of protein-ligand and intra-protein interactions (αB-αF, αJ-αB, αJ-αF, ASL-αD and ASL-αF interfaces) were conducted with quantum chemistry methods (GFN2-xTB and IGMH). It suggested that the residues adjacent to Asp766 in the HD and ASL domains and the αJ-αF and ASL-αD interfaces were closely related to the selectivity and trapping mechanism. These results would provide some insights for the design and development of novel PARP-1/2 inhibitors with improved pharmacodynamic properties.

PubMed: 40228437
DOI: 10.1016/j.bioorg.2025.108471

実験手法

X-RAY DIFFRACTION (2.1 Å)