(3.231.25.104)
Users online: 2124    [ij] [ij] [ij] 
Email id
 

Research Journal of Pharmacy and Technology
Year : 2018, Volume : 11, Issue : 4
First page : ( 1413) Last page : ( 1420)
Print ISSN : 0974-3618. Online ISSN : 0974-360X.
Article DOI : 10.5958/0974-360X.2018.00264.0

Computational Modeling of Novel Drug Targets ftsE and mpt83 for MDRTB and Molecular Docking of Selected Compounds from Medicinal Plants.

Suresh M. Xavier*, Mahalakshmi J. A., Vinisha G.

Department of Physics, (DST-FIST Sponsored), Sathyabama University, Chennai-600119

*Corresponding Author E-mail: xaviersuresh@gmail.com

Online published on 24 July, 2018.

Abstract

Tuberculosis is the major health problem in public and it is an urgent need to find novel targets and drugs because of emergence of multiple drug resistant strains of Mycobacterium tuberculosis. The NGS data of the most virulent H37RV strain is retrieved from NCBI, SRA database and analyzed. Molecular modeling and docking studies between the homology modeled drug targets and the selected drug molecules and herbal compounds were carried out using Ligandfit in Accelrys Discovery Studio. Further, molecular docking analysis revealed that the targets ftsE and mpt83, known to be novel targets and this study has paved way for using herbal compound Allicin from Allium sativum as potential constituents to the prevention of TB.

Top

Keywords

Mycobacterium tuberculosis, Homology modeling, docking, ADMET.

Top

  
║ Site map ║ Privacy Policy ║ Copyright ║ Terms & Conditions ║ Page Rank Tool
436,050,160 visitor(s) since 30th May, 2005.
All rights reserved. Site designed and maintained by DIVA ENTERPRISES PVT. LTD..
Note: Please use Internet Explorer (6.0 or above). Some functionalities may not work in other browsers.