4IKA

Crystal structure of EV71 3Dpol-VPg

4IKA の概要

• エントリーDOI: 10.2210/pdb4ika/pdb
• 分子名称: 3Dpol, VPg, NICKEL (II) ION, ... (4 entities in total)
• 機能のキーワード: rdrp, replication, vpg
• 由来する生物種: Human enterovirus 71; 詳細
• 細胞内の位置: Host cytoplasm (By similarity). Host cytoplasmic vesicle membrane; Peripheral membrane protein; Cytoplasmic side (By similarity). Virion (By similarity): I3UIB4 Q0ZSY4
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 55023.76

構造登録者

Chen, C.,Wang, Y.X.,Lou, Z.Y. (登録日: 2012-12-25, 公開日: 2013-09-04, 最終更新日: 2023-11-08)

主引用文献

Chen, C.,Wang, Y.X.,Shan, C.,Sun, Y.,Xu, P.,Zhou, H.G.,Yang, C.,Shi, P.Y.,Rao, Z.H.,Zhang, B.,Lou, Z.Y.
Crystal structure of enterovirus 71 RNA-dependent RNA polymerase complexed with its protein primer VPg: implication for a trans mechanism of VPg uridylylation
J.Virol., 87:5755-5768, 2013

PubMed Abstract: Picornavirus RNA replication is initiated by VPg uridylylation, during which the hydroxyl group of the third tyrosine residue of the virally encoded protein VPg is covalently linked to two UMP molecules by RNA-dependent RNA polymerase (RdRp; also known as 3D(pol)). We previously identified site 311, located at the base of the palm domain of the enterovirus 71 (EV71) RdRp, to be the site for EV71 VPg binding and uridylylation. Here we report the crystal structure of EV71 3D(pol) complexed with VPg. VPg was anchored at the bottom of the palm domain of the 3D(pol) molecule and exhibited an extended V-shape conformation. The corresponding interface on 3D(pol) was mainly formed by residues within site 311 and other residues in the palm and finger domains. Mutations of the amino acids of 3D(pol) involved in the VPg interaction (3DL319A, 3DD320A, and 3DY335A) significantly disrupted VPg binding to 3D(pol), resulting in defective VPg uridylylation. In contrast, these mutations did not affect the RNA elongation activity of 3D(pol). In the context of viral genomic RNA, mutations that abolished VPg uridylylation activity were lethal for EV71 replication. Further in vitro analysis showed that the uridylylation activity was restored by mixing VPg-binding-defective and catalysis-defective mutants, indicating a trans mechanism for EV71 VPg uridylylation. Our results, together with previous results of other studies, demonstrate that different picornaviruses use distinct binding sites for VPg uridylylation.

PubMed: 23487447
DOI: 10.1128/JVI.02733-12

実験手法

X-RAY DIFFRACTION (2.7 Å)