Article (Scientific journals)
Implications of Binding Mode and Active Site Flexibility for Inhibitor Potency against the Salicylate Synthase from Mycobacterium tuberculosis
Chi, Gamma; Manos-Turvey, Alexandra; O’Connor, Patrick D. et al.
2012In Biochemistry, 51 (24), p. 4868-4879
Peer Reviewed verified by ORBi
 

Files


Full Text
2012 Biochemistry of Gammi Chi.pdf
Publisher postprint (2.25 MB)
Request a copy

All documents in ORBi are protected by a user license.

Send to



Details



Abstract :
[en] MbtI is the salicylate synthase that catalyzes the first committed step in the synthesis of the iron chelating compound mycobactin in Mycobacterium tuberculosis. We previously developed a series of aromatic inhibitors against MbtI based on the reaction intermediate for this enzyme, isochorismate. The most potent of these inhibitors had hydrophobic substituents, ranging in size from a methyl to a phenyl group, appended to the terminal alkene of the enolpyruvyl group. These compounds exhibited low micromolar inhibition constants against MbtI and were at least an order of magnitude more potent than the parental compound for the series, which carries a native enolpyruvyl group. In this study, we sought to understand how the substituted enolpyruvyl group confers greater potency, by determining cocrystal structures of MbtI with six inhibitors from the series. A switch in binding mode at the MbtI active site is observed for inhibitors carrying a substituted enolpyruvyl group, relative to the parental compound. Computational studies suggest that the change in binding mode, and higher potency, is due to the effect of the substituents on the conformational landscape of the core inhibitor structure. The crystal structures and fluorescence-based thermal shift assays indicate that substituents larger than a methyl group are accommodated in the MbtI active site through significant but localized flexibility in the peptide backbone. These findings have implications for the design of improved inhibitors of MbtI, as well as other chorismate-utilizing enzymes from this family.
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Chi, Gamma
Manos-Turvey, Alexandra ;  University of Sydney > School of Chemistry
O’Connor, Patrick D.
Johnston, Jodie M.
Evans, Genevieve L.
Baker, Edward N.
Payne, Richard J.
Lott, J. Shaun
Bulloch, Esther M. M.
Language :
English
Title :
Implications of Binding Mode and Active Site Flexibility for Inhibitor Potency against the Salicylate Synthase from Mycobacterium tuberculosis
Publication date :
2012
Journal title :
Biochemistry
ISSN :
0006-2960
eISSN :
1520-4995
Publisher :
American Chemical Society, Washington, United States - District of Columbia
Volume :
51
Issue :
24
Pages :
4868-4879
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 03 June 2016

Statistics


Number of views
80 (1 by ULiège)
Number of downloads
0 (0 by ULiège)

Scopus citations®
 
36
Scopus citations®
without self-citations
32
OpenCitations
 
28
OpenAlex citations
 
37

Bibliography


Similar publications



Contact ORBi