6VUQ

Crystal structure of CHIKV nsP3 macrodomain soaked with ADP-ribose

6VUQ の概要

• エントリーDOI: 10.2210/pdb6vuq/pdb
• 分子名称: Nonstructural polyprotein, ADENOSINE-5-DIPHOSPHORIBOSE (3 entities in total)
• 機能のキーワード: nsp3, macrodomain, viral protein
• 由来する生物種: Chikungunya virus (CHIKV)
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 76312.77

構造登録者

Wu, M. (登録日: 2020-02-16, 公開日: 2021-01-13, 最終更新日: 2023-10-11)

主引用文献

Zhang, S.,Garzan, A.,Haese, N.,Bostwick, R.,Martinez-Gzegozewska, Y.,Rasmussen, L.,Streblow, D.N.,Haise, M.T.,Pathak, A.K.,Augelli-Szafran, C.E.,Wu, M.
Pyrimidone inhibitors targeting Chikungunya Virus nsP3 macrodomain by fragment-based drug design.
Plos One, 16:e0245013-e0245013, 2021

PubMed Abstract: The macrodomain of nsP3 (nsP3MD) is highly conserved among the alphaviruses and ADP-ribosylhydrolase activity of Chikungunya Virus (CHIKV) nsP3MD is critical for CHIKV viral replication and virulence. No small molecule drugs targeting CHIKV nsP3 have been identified to date. Here we report small fragments that bind to nsP3MD which were discovered by virtually screening a fragment library and X-ray crystallography. These identified fragments share a similar scaffold, 2-pyrimidone-4-carboxylic acid, and are specifically bound to the ADP-ribose binding site of nsP3MD. Among the fragments, 2-oxo-5,6-benzopyrimidine-4-carboxylic acid showed anti-CHIKV activity with an IC50 of 23 μM. Our fragment-based drug discovery approach provides valuable information to further develop a specific and potent nsP3 inhibitor of CHIKV viral replication based on the 2-pyrimidone-4-carboxylic acid scaffold. In silico studies suggest this pyrimidone scaffold could also bind to the macrodomains of other alphaviruses and coronaviruses and thus, have potential pan-antiviral activity.

PubMed: 33482665
DOI: 10.1371/journal.pone.0245013

実験手法

X-RAY DIFFRACTION (1.64 Å)