Department of Biotechnology, Rama University, India
*Corresponding author: Vivek Srivastava, Department of Biotechnology, Faculty of Engineering & Technology, Rama University Uttar Pradesh Kanpur, India
Submission: June 15, 2018; Published: July 25, 2018
ISSN 2578-0247Volume2 Issue2
Dengue and Zika fever are mosquito-borne viral diseases that have rapidly spread in all over world. Currently there are no specific drugs for DENV and ZIKV infection. The recent outbreak of these viruses realized that there are major health risks, demands an enhanced surveillance and a need to develop novel drugs against them. Non-structural proteins NS5 and NS3 are essential for the replication of the flavi-viral RNA genome. Therefore its inhibition could be considered as a useful strategy for treatment of DENV and ZIKV infection. Quinacrine and Berberine had been docked with NS5-methyltransferase of Dengue virus and NS3 protein of ZIKV using Auto dock 4.2 tools. Quinacrine and Berberine showed binding affinity -6.83kcal/mol and -6.22kcal/mol with NS5-methyltransferase and -7.32kcal/mol and -8.03kcal/mol with NS3 protease of ZIKV, respectively. Observations discussion in review will be useful in designing single drug against both virus infections..
Keywords: NS3 protease; NS5-methyltransferase; Antiviral drugs; Dengue virus; Zika virus