6ADY

Crystal structure of the Zika virus NS3 helicase (ADP-Mn2+ complex, form 2)

6ADY の概要

• エントリーDOI: 10.2210/pdb6ady/pdb
• 分子名称: Serine protease NS3, ADENOSINE-5'-DIPHOSPHATE, MANGANESE (II) ION, ... (4 entities in total)
• 機能のキーワード: zika virus ns3 helicase, adp-mn2+ complex, hydrolase
• 由来する生物種: Zika virus (strain Mr 766) (ZIKV)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 50894.69

構造登録者

Fang, J.,Lu, G.,Gong, P. (登録日: 2018-08-02, 公開日: 2019-03-13, 最終更新日: 2023-11-22)

主引用文献

Fang, J.,Jing, X.,Lu, G.,Xu, Y.,Gong, P.
Crystallographic Snapshots of the Zika Virus NS3 Helicase Help Visualize the Reactant Water Replenishment.
ACS Infect Dis, 5:177-183, 2019

PubMed Abstract: Zika virus (ZIKV), a positive-strand RNA virus belonging to the Flavivirus genus, has become an urgent public health concern since recent outbreaks worldwide. Its genome replication is facilitated by the viral NS3 protein bearing helicase function. The NS3 helicase uses energy derived from adenosine triphosphate (ATP) hydrolysis to unwind RNA duplexed regions. Structural studies of the flavivirus NS3 helicases have suggested a conserved mechanism of ATP hydrolysis. However, the process of the reactant water replenishment, a key part of the hydrolysis cycle, remains elusive. Here, we report two high-resolution crystal structures of ZIKV NS3 helicase in complex with adenosine diphosphate (ADP) and Mn, one with the reactant water already loaded as previously observed and the other with the water molecule still in a loading state. These data suggest that the reactant water replenishment can occur between the release of phosphate and the release of ADP and improves the structural basis of the NS3 ATP hydrolysis cycle.

PubMed: 30672289
DOI: 10.1021/acsinfecdis.8b00214

実験手法

X-RAY DIFFRACTION (1.9 Å)