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J Biomol Struct Dyn. 2015;33(2):344-64. doi: 10.1080/07391102.2013.872052. Epub 2014 Jan 13.

3D-QSAR studies and shape based virtual screening for identification of novel hits to inhibit MbtA in Mycobacterium tuberculosis.

Author information

1
a Structural Biology and Bioinformatics Division, CSIR-Indian Institute of Chemical Biology , 4 Raja S.C. Mullick Road, Jadavpur, Kolkata 700032 , India.

Abstract

Mycobacterium tuberculosis, the pathogen responsible for tuberculosis, uses various strategies to survive in a variety of host lesions. The re-emergence of multi-drug-resistant strains of M. tuberculosis underlines the necessity to discover new molecules. Inhibitors of aryl acid adenylating enzyme, MbtA, involved in siderophore biosynthesis in M. tuberculosis, are being explored as potential anti tubercular agents. In this study, we have used 3D-QSAR models and shape based virtual screening to identify novel MbtA inhibitors. 3D-QSAR studies were carried out on nucleoside bisubstrate derivatives. Both Comparative Molecular Field Analysis (r(2) = .944 and r(2)(pred) = .938) and Comparative Molecular Similarity Indices Analysis (r(2) = .892 and r(2)(pred) = .842) models, developed using Gasteiger charges with all fields, predicted efficiently. A total of 13 hits were identified as novel prospective inhibitors for MbtA by utilizing an insilico workflow. Out of 13 hits, five top ranked hits were used for further molecular dynamics studies to gain more insights about the stability of the complexes.

KEYWORDS:

3D-QSAR; MD simulation; docking; shape based virtual screening; tuberculosis

PMID:
24417439
DOI:
10.1080/07391102.2013.872052
[Indexed for MEDLINE]

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