8JED

Crystal structure of mRNA cap (guanine-N7) methyltransferase E12 subunit from monkeypox virus and discovery of its inhibitors

8JED の概要

• エントリーDOI: 10.2210/pdb8jed/pdb
• 分子名称: mRNA-capping enzyme regulatory subunit OPG124 (2 entities in total)
• 機能のキーワード: monkeypox virus, n7-methyltransferase e12 subunit, inhibitors, transferase
• 由来する生物種: Monkeypox virus
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 34663.89

構造登録者

Wang, D.,Zhao, R.,Shu, W.,Hu, W.,Wang, M.,Cao, J.,Zhou, X. (登録日: 2023-05-15, 公開日: 2023-12-06)

主引用文献

Wang, D.P.,Zhao, R.,Wang, H.F.,Wang, M.Y.,Hu, W.S.,Lin, M.M.,Shu, W.,Sun, Y.J.,Cao, J.M.,Cui, W.,Zhou, X.
Crystal structure of mRNA cap (guanine-N7) methyltransferase E12 subunit from monkeypox virus and discovery of its inhibitors.
Int.J.Biol.Macromol., 253:127565-127565, 2023

PubMed Abstract: In July 2022, the World Health Organization announced monkeypox as a public health emergency of international concern (PHEIC), and over 85,000 global cases have been reported currently. However, preventive and therapeutic treatments for the monkeypox virus (MPXV) remain limited. MPXV mRNA cap N7 methyltransferase (MTase) is composed of two subunits (E1 C-terminal domain (E1) and E12) which are essential for the replication of MPXV. Here, we solved a 2.16 Å crystal structure of E12. We also docked the D1 of the vaccinia virus (VACV) corresponding to the E1 in MPXV with E12 and found critical residues at their interface. These residues were further used for drug screening. After virtual screening, the top 347 compounds were screened out and a list of top 20 potential MPXV E12 inhibitors were discovered, including Rutin, Quercitrin, Epigallocatechin, Rosuvastatin, 5-hydroxy-L-Tryptophan, and Deferasirox, etc., which were potential E12 inhibitors. Taking the advantage of the previously unrecognized special structure of MPXV MTase composing of E1 and E12 heterodimer, we screened for inhibitors targeting MTase for the first time based on the interface between the heterodimer of MPXV MTase. Our study may provide insights into the development of anti-MPXV drugs.

PubMed: 37866584
DOI: 10.1016/j.ijbiomac.2023.127565

実験手法

X-RAY DIFFRACTION (2.16 Å)