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Molecular Docking Studies of E-Bola Virus Protein VP30
Authors(2) :-Uzma Paveen A. Shaikh, Yogesh N. Joshi
The Ebola virus (EBOV) genome encodes for several proteins that are necessary and sufficient for replication and transcription of the viral RNAs; NP, VP30, VP35, and L. VP30.VP30 binds to the RNA at the first gene start signal to initiate transcription. VP30 protein has playing important role in Ebola virus transcription and transcription reinitiation hence VP30 protein was targeted for the inhibition of Ebola virus. After target identification, Framycetin drug was taken from DrugBank database which is new lead and its derivatives were designed by bioinformatics virtual screening. Further, drug lead molecules were evaluated for their drug likeness using “Lipinski rule of five” and pharmacokinetic/ADMET properties. In molecular docking studies framycetin derivative shows the better binding energy with the target protein. This in silico approach can be appropriate to develop new drug lead molecules against Vp30 proteins Ebola virus infection.
Uzma Paveen A. Shaikh, Yogesh N. Joshi
Keywords: Ebola virus, VP30, framycetin, virtual screening, Molecular docking.
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Published in : Volume 2 | Issue 1 | January-February 2016
Date of Publication : 2016-03-05
License: This work is licensed under a Creative Commons Attribution 4.0 International License.
Page(s) : 93-98
Manuscript Number : IJSRST162121
Publisher : Technoscience Academy
PRINT ISSN : 2395-6011
ONLINE ISSN : 2395-602X
Cite This Article :
Uzma Paveen A. Shaikh, Yogesh N. Joshi, "Molecular Docking Studies of E-Bola Virus Protein VP30", International Journal of Scientific Research in Science and Technology(IJSRST), Print ISSN : 2395-6011, Online ISSN : 2395-602X, Volume 2, Issue 1, pp.93-98, January-February-2016
URL : http://ijsrst.com/IJSRST162121