9KU2

Structure of taterapox core protease central domain

Summary for 9KU2

• Entry DOI: 10.2210/pdb9ku2/pdb
• Descriptor: Viral core cysteine proteinase (2 entities in total)
• Functional Keywords: orthopoxvirus, mpox, protease, viral protein
• Biological source: Taterapox virus
• Total number of polymer chains: 1
• Total formula weight: 49419.86

Authors

Li, D.,Wang, H.,Ji, X.,Gao, Y.,Wang, W.,Yang, H. (deposition date: 2024-12-03, release date: 2025-03-12, Last modification date: 2025-09-24)

Primary citation

Gao, Y.,Xie, X.,Zhang, X.,Cao, J.,Lan, W.,You, T.,Li, D.,Dong, X.,Dai, W.,Xiang, Y.,Hu, S.,Shang, W.,Wu, B.,Zhang, Y.,Xu, J.,Liu, X.,Wang, H.,Hu, W.,Zhang, M.,Duan, Y.,Cui, W.,Zhou, H.,Mao, S.,Jia, H.,Sun, Z.,Jia, M.,Yin, Y.,Nguyen, H.C.,Yang, K.,Yang, B.,Yang, X.,Ji, X.,Xiao, G.,Wang, W.,Zhang, L.,Rao, Z.,Liu, H.,Yang, H.
Substrate recognition and cleavage mechanism of the monkeypox virus core protease.
Nature, 643:271-279, 2025

PubMed Abstract: Poxviruses cause severe diseases, including smallpox and mpox, that pose major threats to human health. The poxvirus core protease (Core) is essential for viral maturation and is highly conserved in poxviruses, making it an attractive antiviral target. However, the structure of Core remains unknown, hampering antiviral development. Here we determined the apo structure of monkeypox virus (MPXV) Core and the structure of Core in a complex with the inhibitor aloxistatin, a drug candidate for muscular dystrophy. These structures show that Core forms a homodimer that features a unique 'dancing couple' fold. The catalytic intermediate state of Core was characterized by an aldehyde derivative from a natural substrate (I-G18). This derivative binds covalently to the catalytic Cys328, shifting the active site of the viral protease from a closed conformation in the apo form to a favourable open conformation upon substrate binding. On the basis of the Core-I-G18 complex, we designed a series of peptidomimetic inhibitors with a nitrile warhead, which could covalently anchor with the catalytic Cys328. These compounds inhibit Core with half-maximal inhibitory concentrations of 44.9-100.3 nM, and exhibit potent and broad anti-poxvirus activity. Our studies provide a basis for designing wide-spectrum inhibitors against poxvirus infections.

PubMed: 40262633
DOI: 10.1038/s41586-025-09014-x

Experimental method

X-RAY DIFFRACTION (1.895 Å)