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A novel small-molecule compound disrupts influenza A virus PB2 cap-binding and inhibits viral replication
Author(s) -
Shuofeng Yuan,
Hin Chu,
Ke Zhang,
Jiahui Ye,
Kailash Singh,
Richard Y. T. Kao,
Bkc Chow,
Jie Zhou,
BoJian Zheng
Publication year - 2016
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkw194
Subject(s) - docking (animal) , viral replication , influenza a virus , polymerase , binding site , biology , ligand binding assay , virus , virology , replicon , microbiology and biotechnology , chemistry , biochemistry , enzyme , receptor , plasmid , gene , medicine , nursing
The conserved residues 318-483 in the PB2 subunit of influenza A polymerase is an independently folded cap-binding domain (PB2cap) that exhibits a distinct binding mode from other host cap-binding proteins, which suggests that PB2cap might be an ideal drug target. This study aimed to identify a new class of anti-influenza inhibitors that specifically disrupts the interaction between PB2cap and host cap structures.

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