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Journal Article

The crystal structure of mycobacterial epoxide hydrolase A

MPS-Authors
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Schulz,  E.-C.
Miller Group, Atomically Resolved Dynamics Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;
European Molecular Biology Laboratory, Hamburg Unit;

External Resource
Fulltext (public)

s41598-020-73452-y.pdf
(Publisher version), 5MB

Supplementary Material (public)

41598_2020_73452_MOESM1_ESM.pdf
(Supplementary material), 9MB

Citation

Schulz, E.-C., Henderson, S. R., Illarionov, B., Crosskey, T., Southall, S. M., Krichel, B., et al. (2020). The crystal structure of mycobacterial epoxide hydrolase A. Scientific Reports, 10(1): 16539. doi:10.1038/s41598-020-73452-y.


Cite as: http://hdl.handle.net/21.11116/0000-0007-36FC-1
Abstract
The human pathogen Mycobacterium tuberculosis is the causative agent of tuberculosis resulting in over 1 million fatalities every year, despite decades of research into the development of new anti-TB compounds. Unlike most other organisms M. tuberculosis has six putative genes for epoxide hydrolases (EH) of the α/β-hydrolase family with little known about their individual substrates, suggesting functional significance for these genes to the organism. Due to their role in detoxification, M. tuberculosis EH’s have been identified as potential drug targets. Here, we demonstrate epoxide hydrolase activity of M. thermoresistibile epoxide hydrolase A (Mth-EphA) and report its crystal structure in complex with the inhibitor 1,3-diphenylurea at 2.0 Å resolution. Mth-EphA displays high sequence similarity to its orthologue from M. tuberculosis and generally high structural similarity to α/β-hydrolase EHs. The structure of the inhibitor bound complex reveals the geometry of the catalytic residues and the conformation of the inhibitor. Comparison to other EHs from mycobacteria allows insight into the active site plasticity with respect to substrate specificity. We speculate that mycobacterial EHs may have a narrow substrate specificity providing a potential explanation for the genetic repertoire of epoxide hydrolase genes in M. tuberculosis.