Recent Advances in Chemical Tools for the Regulation and Study of Protein Lysine Methyltransferases

被引:3
|
作者
Hirano, Tomoya [1 ]
Mori, Shuichi [1 ]
Kagechika, Hiroyuki [1 ]
机构
[1] Tokyo Med & Dent Univ, Inst Biomat & Bioengn, Chiyoda Ku, 2-3-10 Kanda Surugadai, Tokyo 1010062, Japan
来源
CHEMICAL RECORD | 2018年 / 18卷 / 12期
关键词
protein lysine methyltransferases; histone; epigenetics; SMALL-MOLECULE INHIBITOR; SELECTIVE INHIBITOR; DOT1L INHIBITORS; COMPETITIVE INHIBITOR; HISTONE MODIFICATIONS; CHROMATIN-STRUCTURE; STRUCTURAL BASIS; COFACTOR ANALOG; RECEPTOR-ALPHA; EZH2; INHIBITOR;
D O I
10.1002/tcr.201800034
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Protein lysine methyltransferases (PKMTs) are epigenetic regulators that modulate gene transcription and physiological functions by catalyzing the post-translational methylation of specific lysine residues of substrate proteins, such as histones. They are considered to be candidate drugs for the treatment of various diseases, including acute myeloid leukemia, and in the past decade, potent and selective inhibitors of individual PKMTs have been developed. Some are currently under clinical trial. In this review, we will focus on some breakthrough PKMT inhibitors, and discuss chemistry-based methods available for elucidation of the physiological functions of PKMTs and methylated proteins.
引用
收藏
页码:1745 / 1759
页数:15
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