Identification of and Structural Insights into Hit Compounds Targeting N-Myristoyltransferase for Cryptosporidium Drug Development

Bicyclic azetidines target acute and chronic stages of Toxoplasma gondii by inhibiting parasite phenylalanyl t-RNA synthetase

Design and synthesis of inhibitors of Plasmodium falciparum N- myristoyltransferase, a promising target for antimalarial drug discovery. - Abstract - Europe PMC

Targeting RNA structures with small molecules

Structure-Based Design of Potent and Selective Leishmania N- Myristoyltransferase Inhibitors

Identification of and Structural Insights into Hit Compounds Targeting N- Myristoyltransferase for Cryptosporidium Drug Development

Frontiers Cryptosporidium parvum Pyruvate Kinase Inhibitors With in vivo Anti-cryptosporidial Efficacy

Modification pattern of proteins starting with glycine iceLogo 1.2 was

Contacts between SC-58272 and Nmt1p.a, Contact distances (Å). The

Discovery of a Novel Class of Orally Active Trypanocidal N- Myristoyltransferase Inhibitors

Structure-Based Design of Potent and Selective Leishmania N- Myristoyltransferase Inhibitors

SIRT2 removes ARF6 K3 myristoylation a Alk12 labeling results on