Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/80089
Title: Functional interplay among the flavivirus NS3 protease, helicase, and cofactors
Authors: Li, Kuohan
Phoo, Wint Wint
Luo, Dahai
Keywords: DRNTU::Science::Medicine
Issue Date: 2014
Source: Li, K., Phoo, W. W., & Luo, D. (2014). Functional interplay among the flavivirus NS3 protease, helicase, and cofactors. Virologica Sinica, 29(2), 74-85.
Series/Report no.: Virologica sinica
Abstract: Flaviviruses are positive-sense RNA viruses, and many are important human pathogens. Nonstructural protein 2B and 3 of the flaviviruses (NS2BNS3) form an endoplasmic reticulum (ER) membraneassociated hetero-dimeric complex through the NS2B transmembrane region. The NS2BNS3 complex is multifunctional. The N-terminal region of NS3, and its cofactor NS2B fold into a protease that is responsible for viral polyprotein processing, and the C-terminal domain of NS3 possesses NTPase/RNA helicase activities and is involved in viral RNA replication and virus particle formation. In addition, NS2BNS3 complex has also been shown to modulate viral pathogenesis and the host immune response. Because of the essential functions that the NS2BNS3 complex plays in the flavivirus life cycle, it is an attractive target for antiviral development. This review focuses on the recent biochemical and structural advances of NS2BNS3 and provides a brief update on the current status of drug development targeting this viral protein complex.
URI: https://hdl.handle.net/10356/80089
http://hdl.handle.net/10220/19288
ISSN: 1674-0769
DOI: 10.1007/s12250-014-3438-6
Rights: © 2014 WIV, CAS and Springer-Verlag Berlin Heidelberg. This is the author created version of a work that has been peer reviewed and accepted for publication by Virologica Sinica, WIV, CAS and Springer-Verlag Berlin Heidelberg. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1007/s12250-014-3438-6].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:LKCMedicine Journal Articles

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