4UFY

Crystal structure of human tankyrase 2 in complex with TA-13

4UFY の概要

• エントリーDOI: 10.2210/pdb4ufy/pdb
• 関連するPDBエントリー: 4UFU
• 分子名称: TANKYRASE-2, ZINC ION, SULFATE ION, ... (6 entities in total)
• 機能のキーワード: transferase, protein-ligand complex, diphtheria toxin like fold, adp- ribosylation, transferase-transferase inhibitor complex
• 由来する生物種: HOMO SAPIENS (HUMAN)
• 細胞内の位置: Cytoplasm: Q9H2K2
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 55891.47

構造登録者

Haikarainen, T.,Lehtio, L. (登録日: 2015-03-20, 公開日: 2016-04-13, 最終更新日: 2024-05-08)

主引用文献

Nathubhai, A.,Haikarainen, T.,Hayward, P.C.,Munoz-Descalzo, S.,Thompson, A.S.,Lloyd, M.D.,Lehtio, L.,Threadgill, M.D.
Structure-Activity Relationships of 2-Arylquinazolin-4-Ones as Highly Selective and Potent Inhibitors of the Tankyrases.
Eur.J.Med.Chem., 118:316-, 2016

PubMed Abstract: Tankyrases (TNKSs), members of the PARP (Poly(ADP-ribose)polymerases) superfamily of enzymes, have gained interest as therapeutic drug targets, especially as they are involved in the regulation of Wnt signalling. A series of 2-arylquinazolin-4-ones with varying substituents at the 8-position was synthesised. An 8-methyl group (compared to 8-H, 8-OMe, 8-OH), together with a 4'-hydrophobic or electron-withdrawing group, provided the most potency and selectivity towards TNKSs. Co-crystal structures of selected compounds with TNKS-2 revealed that the protein around the 8-position is more hydrophobic in TNKS-2 compared to PARP-1/2, rationalising the selectivity. The NAD(+)-binding site contains a hydrophobic cavity which accommodates the 2-aryl group; in TNKS-2, this has a tunnel to the exterior but the cavity is closed in PARP-1. 8-Methyl-2-(4-trifluoromethylphenyl)quinazolin-4-one was identified as a potent and selective inhibitor of TNKSs and Wnt signalling. This compound and analogues could serve as molecular probes to study proliferative signalling and for development of inhibitors of TNKSs as drugs.

PubMed: 27163581
DOI: 10.1016/J.EJMECH.2016.04.041

実験手法

X-RAY DIFFRACTION (1.7 Å)