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Updated: Mar 9, 2026

Assays for Validating Histone Acetyltransferase Inhibitors
Published on: August 6, 2020
Turning a Substrate Peptide into a Potent Inhibitor for the Histone Methyltransferase SETD8
Russell A Judge1, Haizhong Zhu1, Anup K Upadhyay1
1AbbVie Inc. , 1 North Waukegan Road, North Chicago, Illinois 60064, United States.
Abstract:
SETD8 is a histone H4-K20 methyltransferase that plays an essential role in the maintenance of genomic integrity during mitosis and in DNA damage repair, making it an intriguing target for cancer research. While some small molecule inhibitors for SETD8 have been reported, the structural binding modes for these inhibitors have not been revealed. Using the complex structure of the substrate peptide bound to SETD8 as a starting point, different natural and unnatural amino acid substitutions were tested, and a potent (Ki 50 nM, IC50 0.33 μM) and selective norleucine containing peptide inhibitor has been obtained.
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