Jump to main content
Jump to site search

Issue 6, 2017
Previous Article Next Article

Differential flap dynamics in L,D-transpeptidase2 from mycobacterium tuberculosis revealed by molecular dynamics

Author affiliations

Abstract

Despite the advances in tuberculosis treatment, TB is still one the most deadly infectious diseases and remains a major global health quandary. Mycobacterium tuberculosis (Mtb) is the only known mycobacterium with a high content of 3→3 crosslinks in the biosynthesis of peptidoglycan, which is negligible in most bacterial species. An Mtb lacking LdtMt2 leads to alteration of the colony morphology and loss of virulence which makes this enzyme an attractive target. Regardless of the vital role of LdtMt2 for cell wall survival, the impact of ligand binding on the dynamics of the β-hairpin flap is still unknown. Understanding the structural and dynamical behaviour of the flap regions provides clear insight into the design of the effective inhibitors against LdtMt2. Carbapenems, an specific class of β-lactam family, have been shown to inactivate this enzyme. Herein a comprehensive investigation of the flap dynamics of LdtMt2 complex with substrate and three carbapenems namely, ertapenem, imipenem and meropenem is discussed and analyzed for the first account using 140 ns molecular dynamics simulations. The structural features (RMSD, RMSF and Rg) derived by MD trajectories were analyzed. Distance analysis, particularly tip–tip SER135–ASN167 index, identified conformational changes in terms of flap opening and closure within binding process. Principal component analysis (PCA) was employed to qualitatively understand the divergent effects of different inhibitors on the dominant motion of each residue. To probe different internal dynamics induced by ligand binding, dynamic cross-correlation marix (DCCM) analysis was used. The binding free energies of the selected complexes were assessed using MM-GBSA method and per residue free energy decomposition analysis were performed to characterize the contribution of the key residues to the total binding free energies.

Graphical abstract: Differential flap dynamics in l,d-transpeptidase2 from mycobacterium tuberculosis revealed by molecular dynamics

Back to tab navigation

Supplementary files

Publication details

The article was received on 23 Feb 2017, accepted on 25 Apr 2017 and first published on 08 May 2017


Article type: Paper
DOI: 10.1039/C7MB00110J
Citation: Mol. BioSyst., 2017,13, 1223-1234
  •   Request permissions

    Differential flap dynamics in L,D-transpeptidase2 from mycobacterium tuberculosis revealed by molecular dynamics

    Z. Fakhar, T. Govender, G. E. M. Maguire, G. Lamichhane, R. C. Walker, H. G. Kruger and B. Honarparvar, Mol. BioSyst., 2017, 13, 1223
    DOI: 10.1039/C7MB00110J

Search articles by author

Spotlight

Advertisements