Summary information and primary citation
- PDB-id
- 8hg1; SNAP-derived features in text and JSON formats;
DNAproDB
- Class
- replication-DNA
- Method
- cryo-EM (2.8 Å)
- Summary
- The structure of mpxv polymerase holoenzyme in replicating state
- Reference
- Peng Q, Xie Y, Kuai L, Wang H, Qi J, Gao GF, Shi Y (2023): "Structure of monkeypox virus DNA polymerase holoenzyme." Science, 379, 100-105. doi: 10.1126/science.ade6360.
- Abstract
- The World Health Organization announced mpox (or monkeypox) as a public health emergency of international concern in July 2022, and prophylactic and therapeutic measures are in urgent need. The monkeypox virus (MPXV) has its own DNA polymerase F8, together with the processive cofactors A22 and E4, constituting the polymerase holoenzyme for genome replication. Here, we determined the holoenzyme structure in complex with DNA using cryo-electron microscopy at the global resolution of ~2.8 Å. The holoenzyme possesses an architecture that suggests a "forward sliding clamp" processivity mechanism for viral DNA replication. MPXV polymerase has a similar DNA binding mode to other B-family DNA polymerases from different species. These findings reveal the mechanism of the MPXV genome replication and may guide the development of anti-poxvirus drugs.
