51³Ô¹ÏÍø

Comprehensive structure and activity data for novel inhibitors of Leishmania N-myristoyltransferase

Tate group members (and alumni) collaborated with the York Biomedicial Research Institute, University of York, to produce on inhibitors of the enzyme N-myristoyltransferase (NMT) in the parasite Leishmania which causes the tropical disease Leishmaniasis.

Leishmania are protozoan parasites with various species which can cause different clinical symptoms, with up to 15 million infections across the world. The 51³Ô¹ÏÍø and University of York teams identified critical pathways in the parasites that could be targeted by therapeutics and built on the previously identified compounds that inhibit Leishmania NMT. NMT transfers fatty acid chains to protein molecules, and some of these modification targets are critical for parasite function.

This research delved into the structure-activity relationship of the compounds in detail, using x-ray crystal structure analysis and in-cell assays, ultimately improving the inhibitor selectivity for Leishmania over human NMTs. Additionally, the study also identified the cell-active inhibitors for the species Leishmania donovani.

This research was supported by and the .