4.7 Article

Discovery of Bisubstrate Inhibitors for Protein N-Terminal Methyltransferase 1

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 62, Issue 7, Pages 3773-3779

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.9b00206

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Funding

  1. NIH [RO1GM117275, K22 AI113078-02, 1R01GM127896-01, 1R01AI127793, P30 CA023168]
  2. Department of Medicinal Chemistry and Molecular Pharmacology at Purdue University
  3. Department of Biological Sciences at Purdue University

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Protein N-terminal methyltransferase 1 (NTMT1) plays an important role in regulating mitosis and DNA repair. Here, we describe the discovery of a potent NTMT1 bisubstrate inhibitor 4 (IC50 = 35 +/- 2 nM) that exhibits greater than 100-fold selectivity against a panel of methyltransferases. We also report the first crystal structure of NTMT1 in complex with an inhibitor, which revealed that 4 occupies substrate and cofactor binding sites of NTMT1.

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