Journal
JOURNAL OF MOLECULAR GRAPHICS & MODELLING
Volume 87, Issue -, Pages 204-210Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jmgm.2018.11.009
Keywords
Mycobacterium tuberculosis (M.tb); L,D-transpeptidase 5 (Ldt(Mt5)); QM/MM; ONIOM; Catalytic mechanism
Categories
Funding
- College of Health Sciences (CHS)
- Aspen Pharmacare
- MRC
- NRF
Ask authors/readers for more resources
Tuberculosis (TB) is one of the world's deadliest diseases resulting from infection by the bacterium, Mycobacterium tuberculosis (M.tb). The L,D-transpeptidase enzymes catalyze the synthesis of 3 -> 3 transpeptide linkages which are predominant in the peptidoglycan of the M.tb cell wall. Carbapenems is class of beta-lactams that inactivate L,D-transpeptidases by acylation, although differences in antibiotic side chains modulate drug binding and acylation rates. Herein, we used a two-layered our Own N-layer integrated Molecular Mechanics ONIOM method to investigate the catalytic mechanism of L,D-transpeptidase 5 (Ldt(Mt5)) by beta-lactam derivatives. Ldt(Mt5) complexes with six beta-Iactams, ZINC03788344 (1), ZINC02462884 (2), ZINC03791246 (3), ZINC03808351 (4), ZINC03784242 (5) and ZINC02475683 (6) were simulated. The QM region (high-level) comprises the beta-lactam, one water molecule and the Cys360 catalytic residue, while the rest of the Ldt(Mt5) residues were treated with AMBER force field. The activation energies (Delta G(#)) were calculated with B3LYP, M06-2X and omega B97X density functionals with 6-311++G(2d, 2p) basis set. The Delta G(#) for the acylation of Ldt(Mt5) by the selected (beta-lactams were obtained as 13.67, 20.90, 22.88, 24.29, 27.86 and 28.26 kcal mol(-1) respectively. Several of the compounds showed an improved Delta G(#) when compared to the previously calculated energies for imipenem and meropenem for the acylation step for Ldt(Mt5). This model provides further validation of the catalytic inhibition mechanism of LDTs with atomistic detail. (C) 2018 Elsevier Inc. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available