8FYY

Crystal structure of human PARP1 ART domain bound to inhibitor UKTT5 (compound 10)

8FYY の概要

• エントリーDOI: 10.2210/pdb8fyy/pdb
• 関連するPDBエントリー: 8FYZ 8FZ1 8G0H
• 分子名称: Poly [ADP-ribose] polymerase 1, processed C-terminus, beta-D-fructofuranose-(2-1)-alpha-D-glucopyranose, 2-(4-{[2-(1H-benzimidazol-2-yl)ethyl]carbamoyl}phenyl)-1H-benzimidazole-7-carboxamide, ... (6 entities in total)
• 機能のキーワード: parp, adp-ribose transferase, dna binding protein, dna binding protein-inhibitor complex, dna binding protein/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: 30954.28

構造登録者

Rouleau-Turcotte, E.,Pascal, J.M. (登録日: 2023-01-27, 公開日: 2024-02-07, 最終更新日: 2024-10-16)

主引用文献

Velagapudi, U.K.,Rouleau-Turcotte, E.,Billur, R.,Shao, X.,Patil, M.,Black, B.E.,Pascal, J.M.,Talele, T.T.
Novel modifications of PARP inhibitor veliparib increase PARP1 binding to DNA breaks.
Biochem.J., 481:437-460, 2024

PubMed Abstract: Catalytic poly(ADP-ribose) production by PARP1 is allosterically activated through interaction with DNA breaks, and PARP inhibitor compounds have the potential to influence PARP1 allostery in addition to preventing catalytic activity. Using the benzimidazole-4-carboxamide pharmacophore present in the first generation PARP1 inhibitor veliparib, a series of 11 derivatives was designed, synthesized, and evaluated as allosteric PARP1 inhibitors, with the premise that bulky substituents would engage the regulatory helical domain (HD) and thereby promote PARP1 retention on DNA breaks. We found that core scaffold modifications could indeed increase PARP1 affinity for DNA; however, the bulk of the modification alone was insufficient to trigger PARP1 allosteric retention on DNA breaks. Rather, compounds eliciting PARP1 retention on DNA breaks were found to be rigidly held in a position that interferes with a specific region of the HD domain, a region that is not targeted by current clinical PARP inhibitors. Collectively, these compounds highlight a unique way to trigger PARP1 retention on DNA breaks and open a path to unveil the pharmacological benefits of such inhibitors with novel properties.

PubMed: 38372302
DOI: 10.1042/BCJ20230406

実験手法

X-RAY DIFFRACTION (2.8 Å)