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Molecular Modeling Approach for the Discovery of Escherichia coli O157:H7 Interaction Inhibitors of Natural Product Compounds
Corresponding Author(s) : S. Pitchuanchom
Asian Journal of Chemistry,
Vol. 31 No. 10 (2019): Vol 31 Issue 10
Abstract
The aim of this study is to report the development of Escherichia coli O157:H7 template for structure-based drug design. This template was validated by redocking with crystal ligand I. The results showed a good matching of docked and the crystallographic binding orientations with root mean square deviation (RMSD) less than 2.0 Å. Moreover, the developed template was applied to predict binding mode of 19 known E. coli inhibitors and 40 natural products. The results showed that the binding energy of almost E. coli inhibitors was related to their biological activity. The use of developed E. coli O157:H7 template in automated docking could speed up the process of novel drug discovery by allowing designed inhibitors to be tested computationally before the compounds are synthesized.
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- S.M. Chekabab, J. Paquin-Veillette, C.M. Dozois and J. Harel, FEMS Microbiol. Lett., 341, 1 (2013); https://doi.org/10.1111/1574-6968.12078.
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References
S.M. Chekabab, J. Paquin-Veillette, C.M. Dozois and J. Harel, FEMS Microbiol. Lett., 341, 1 (2013); https://doi.org/10.1111/1574-6968.12078.
R. Jonge, K. Takumi, W.S. Ritmeester and F.M. Leusden, J. Appl. Microbiol., 94, 555 (2003); https://doi.org/10.1046/j.1365-2672.2003.01865.x.
T.R. Callaway, M.A. Carr, T.S. Edrington, R.C. Anderson and D.J. Nisbet, Curr. Issues Mol. Biol., 11, 67 (2009); https://doi.org/10.21775/cimb.011.067.
B. Kenny, A. Abe, M. Stein and B.B. Finlay, Infect. Immun., 65, 2606 (1997).
S.W. Naylor, A. Roe, J. Nart, P.K. Spears, D.G. Smith, J.C. Low and D.L. Gally, Microbiology, 151, 2773 (2005); https://doi.org/10.1099/mic.0.28060-0.
J. Barker, T.J. Humphrey and M.W. Brown, FEMS Microbiol. Lett., 173, 291 (1999); https://doi.org/10.1111/j.1574-6968.1999.tb13516.x.
G. Wang, T. Zhao and M.P. Doyle, Appl. Environ. Microbiol., 62, 2567 (1996).
E.W. Rice and C.H. Johnson, J. Dairy Sci., 83, 2021 (2000); https://doi.org/10.3168/jds.S0022-0302(00)75081-8.
J.W. Yoon, M.K. Park, C.J. Hovde, S.H. Cho, J.C. Kim, M.S. Park and W. Kim, Biochem. Biophys. Res. Commun., 391, 1792 (2010); https://doi.org/10.1016/j.bbrc.2009.12.160.
E.S. Rangarajan, G. Nadeau, Y. Li, J. Wagner, M.N. Hung, J.D. Schrag, M. Cygler and A. Matte, J. Mol. Biol., 359, 1249 (2006); https://doi.org/10.1016/j.jmb.2006.04.031.
D.Y.W. Lin, J. Diao, D. Zhou and J. Chen, J. Biol. Chem., 286, 441 (2011); https://doi.org/10.1074/jbc.M110.167643.
M.D.L. Suits, J. Lang, G.P. Pal, M. Couture and Z. Jia, Protein Sci., 18, 825 (2009); https://doi.org/10.1002/pro.84.
L.M. van Staalduinen, C.-S. Park, S.-J. Yeom, M.A. Adams-Cioaba, D.-K. Oh and Z. Jia, J. Mol. Biol., 401, 866 (2010); https://doi.org/10.1016/j.jmb.2010.06.063.
G.M. Morris, D.S. Goodsell, S. Halliday, R. Huey, W.E. Hart, R.K. Belew and A.J. Olson, J. Comput. Chem., 19, 1639 (1998); https://doi.org/10.1002/(SICI)1096-987X(19981115)19:14<1639::AID-JCC10>3.0.CO;2-B.
S.J. Weiner, P.A. Kollman, D.A. Case, U.C. Singh, C. Ghio, G. Alagona, S. Profeta and P. Weiner, J. Am. Chem. Soc., 106, 765 (1984); https://doi.org/10.1021/ja00315a051.
G.M. Morris, D.S. Goodsell, R. Huey and A.J. Olson, J. Comput. Aided Mol. Des., 10, 293 (1996); https://doi.org/10.1007/BF00124499.
R. La Fuente, N.D. Sonawane, D. Arumainayagam and A.S. Verkman, Br. J. Pharmacol., 149, 551 (2006); https://doi.org/10.1038/sj.bjp.0706873.
L.J. Cseke, A. Kirakosyan, P.B. Kaufman, S.L. Warber, J.A. Duke and H.A. Brielmann, Natural Products from Plants, CRC Press: Boca Raton, FL, edn 2 (2006).