Identification of novel leads applying in silico studies for Mycobacterium multidrug resistant (MMR) protein.

Abstract:

:Multidrug efflux mechanism is the main cause of intrinsic drug resistance in bacteria. Mycobacterium multidrug resistant (MMR) protein belongs to small multidrug resistant family proteins (SMR), causing multidrug resistance to proton (H(+))-linked lipophilic cationic drug efflux across the cell membrane. In the present work, MMR is treated as a novel target to identify new molecular entities as inhibitors for drug resistance in Mycobacterium tuberculosis. In silico techniques are applied to evaluate the 3D structure of MMR protein. The putative amino acid residues present in the active site of MMR protein are predicted. Protein-ligand interactions are studied by docking cationic ligands transported by MMR protein. Virtual screening is carried out with an in-house library of small molecules against the grid created at the predicted active site residues in the MMR protein. Absorption distribution metabolism and elimination (ADME) properties of the molecules with best docking scores are predicted. The studies with cationic ligands and those of virtual screening are analysed for identification of new lead molecules as inhibitors for drug resistance caused by the MMR protein.

journal_name

J Biomol Struct Dyn

authors

Malkhed V,Mustyala KK,Potlapally SR,Vuruputuri U

doi

10.1080/07391102.2013.842185

subject

Has Abstract

pub_date

2014-12-01 00:00:00

pages

1889-906

issue

12

eissn

0739-1102

issn

1538-0254

journal_volume

32

pub_type

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