组氨酸
化学
生物化学
酶
药物发现
甲基转移酶
药品
铅化合物
结构-活动关系
结合位点
计算生物学
血浆蛋白结合
药物靶点
HEK 293细胞
转移酶
药理学
选择性
生物
抑制性突触后电位
蛋白质-蛋白质相互作用
癌症研究
活动站点
酶抑制剂
立体化学
细胞生物学
药物开发
酶激活剂
组合化学
化学生物学
结构生物学
靶蛋白
FKBP公司
蛋白质结构
作者
Rui Yao,Guo Zhang,Yuanting Huang,Danchen Fan,Hailin Zhang,Jingxin Qiao,Chong Chen,Zhenhua Shao,Linli Li,S. Yang
摘要
ABSTRACT Protein histidine N1‐methylation (1‐methylhistidine, 1‐MH) is a prevalent yet underexplored post‐translational modification in mammals. The methyltransferase METTL9 acts as an important enzyme catalyzing 1‐MH of histidine in diverse protein substrates, with mounting evidence suggesting its involvement in tumor progression. Despite its potential significance, no inhibitors targeting METTL9 have been previously identified. Here, we introduce compound METTL9i as a first‐in‐class, highly potent, and selective METTL9 inhibitor. METTL9i inhibits METTL9 with a half‐maximum inhibitory concentration (IC 50 ) of 0.067 ± 0.009 µM and exhibits selectivity over other methyltransferases. Structural analysis via crystallography reveals that METTL9i binds within the S‐adenosylmethionine (SAM) binding pocket. In cells, METTL9i engages METTL9 and leads to a reduction in global 1‐MH levels. These results support METTL9i as a useful tool compound for investigating METTL9 biology and the functions of histidine 1‐MH, while also serving as a promising lead compound for drug discovery targeting METTL9.
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