Structure-based design of diverse inhibitors of Mycobacterium tuberculosis N-acetylglucosamine-1-phosphate uridyltransferase: combined molecular docking, dynamic simulation, and biological activity
Gespeichert in:
Verfasser / Beitragende:
[Vijay Soni, Priyanka Suryadevara, Dharmarajan Sriram, Santhosh Kumar, Vinay Nandicoori, Perumal Yogeeswari]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Molecular Modeling, 21/7(2015-07-01), 1-12
Format:
Artikel (online)
Online Zugang:
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| 024 | 7 | 0 | |a 10.1007/s00894-015-2704-3 |2 doi |
| 035 | |a (NATIONALLICENCE)springer-10.1007/s00894-015-2704-3 | ||
| 245 | 0 | 0 | |a Structure-based design of diverse inhibitors of Mycobacterium tuberculosis N-acetylglucosamine-1-phosphate uridyltransferase: combined molecular docking, dynamic simulation, and biological activity |h [Elektronische Daten] |c [Vijay Soni, Priyanka Suryadevara, Dharmarajan Sriram, Santhosh Kumar, Vinay Nandicoori, Perumal Yogeeswari] |
| 520 | 3 | |a Persistent nature of Mycobacterium tuberculosis is one of the major factors which make the drug development process monotonous against this organism. The highly lipophilic cell wall, which constituting outer mycolic acid and inner peptidoglycan layers, acts as a barrier for the drugs to enter the bacteria. The rigidity of the cell wall is imparted by the peptidoglycan layer, which is covalently linked to mycolic acid by arabinogalactan. Uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc) serves as the starting material in the biosynthesis of this peptidoglycan layers. This UDP-GlcNAc is synthesized by N-acetylglucosamine-1-phosphate uridyltransferase (GlmUMtb), a bi-functional enzyme with two functional sites, acetyltransferase site and uridyltransferase site. Here, we report design and screening of nine inhibitors against UTP and NAcGlc-1-P of uridyltransferase active site of glmUMtb. Compound 4 was showing good inhibition and was selected for further analysis. The isothermal titration calorimetry (ITC) experiments showed the binding energy pattern of compound 4 to the uridyltransferase active site is similar to that of substrate UTP. In silico molecular dynamics (MD) simulation studies, for compound 4, carried out for 10ns showed the protein-compound complex to be stable throughout the simulation with relative rmsd in acceptable range. Hence, these compounds can serve as a starting point in the drug discovery processes against Mycobacterium tuberculosis. Graphical Abstract Superimposed structures of glmuMtb - compound 4 complex collected at various intervals during molecular dynamics simulations displaying the stability of the complex | |
| 540 | |a Springer-Verlag Berlin Heidelberg, 2015 | ||
| 690 | 7 | |a Isothermal titration calorimetry (ITC) |2 nationallicence | |
| 690 | 7 | |a Lipophilic cell wall |2 nationallicence | |
| 690 | 7 | |a Molecular dynamics (MD) simulations |2 nationallicence | |
| 690 | 7 | |a N-acetylglucosamine-1-phosphate uridyltransferase (GlmUMtb) |2 nationallicence | |
| 700 | 1 | |a Soni |D Vijay |u Department of Pharmacy, Birla Institute of Technology & Science-Pilani, Hyderabad campus, Shameerpet, Jawahar Nagar, R.R. District, India |4 aut | |
| 700 | 1 | |a Suryadevara |D Priyanka |u Department of Pharmacy, Birla Institute of Technology & Science-Pilani, Hyderabad campus, Shameerpet, Jawahar Nagar, R.R. District, India |4 aut | |
| 700 | 1 | |a Sriram |D Dharmarajan |u Department of Pharmacy, Birla Institute of Technology & Science-Pilani, Hyderabad campus, Shameerpet, Jawahar Nagar, R.R. District, India |4 aut | |
| 700 | 1 | |a Kumar |D Santhosh |u CSIR-Institute of Genomics and Integrative Biology, Mathura Road, 110020, New Delhi, India |4 aut | |
| 700 | 1 | |a Nandicoori |D Vinay |u National Institute of Immunology, Aruna Asaf Ali Marg, 110067, New Delhi, India |4 aut | |
| 700 | 1 | |a Yogeeswari |D Perumal |u Department of Pharmacy, Birla Institute of Technology & Science-Pilani, Hyderabad campus, Shameerpet, Jawahar Nagar, R.R. District, India |4 aut | |
| 773 | 0 | |t Journal of Molecular Modeling |d Springer Berlin Heidelberg |g 21/7(2015-07-01), 1-12 |x 1610-2940 |q 21:7<1 |1 2015 |2 21 |o 894 | |
| 856 | 4 | 0 | |u https://doi.org/10.1007/s00894-015-2704-3 |q text/html |z Onlinezugriff via DOI |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 900 | 7 | |a Metadata rights reserved |b Springer special CC-BY-NC licence |2 nationallicence | |
| 908 | |D 1 |a research-article |2 jats | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-springer | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1007/s00894-015-2704-3 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Soni |D Vijay |u Department of Pharmacy, Birla Institute of Technology & Science-Pilani, Hyderabad campus, Shameerpet, Jawahar Nagar, R.R. District, India |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Suryadevara |D Priyanka |u Department of Pharmacy, Birla Institute of Technology & Science-Pilani, Hyderabad campus, Shameerpet, Jawahar Nagar, R.R. District, India |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Sriram |D Dharmarajan |u Department of Pharmacy, Birla Institute of Technology & Science-Pilani, Hyderabad campus, Shameerpet, Jawahar Nagar, R.R. District, India |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Kumar |D Santhosh |u CSIR-Institute of Genomics and Integrative Biology, Mathura Road, 110020, New Delhi, India |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Nandicoori |D Vinay |u National Institute of Immunology, Aruna Asaf Ali Marg, 110067, New Delhi, India |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Yogeeswari |D Perumal |u Department of Pharmacy, Birla Institute of Technology & Science-Pilani, Hyderabad campus, Shameerpet, Jawahar Nagar, R.R. District, India |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Journal of Molecular Modeling |d Springer Berlin Heidelberg |g 21/7(2015-07-01), 1-12 |x 1610-2940 |q 21:7<1 |1 2015 |2 21 |o 894 | ||