Structural insights for producing CK2α1-specific inhibitors

被引:4
|
作者
Tsuyuguchi, Masato [1 ]
Nakaniwa, Tetsuko [2 ]
Hirasawac, Akira [3 ]
Nakanishi, Isao [4 ]
Kinoshita, Takayoshi [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Sci, 1-1 Gakuen Cho, Sakai, Osaka 5998531, Japan
[2] Osaka Univ, Inst Prot Res, 3-2 Yamadaoka, Suita, Osaka 5650871, Japan
[3] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
[4] Kindai Univ, Dept Pharmaceut Sci, Fac Pharm, 3-4-1 Kowakae, Higashiosaka, Osaka 5778502, Japan
关键词
CK2; alpha; 1; Selectivity; Binding mode; Crystal structure; Conformational change; PROTEIN-KINASE CK2; CRYSTAL-STRUCTURE; POTENT; CK2-ALPHA-2; DISCOVERY;
D O I
10.1016/j.bmcl.2019.126837
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Casein kinase 2 catalytic subunit (CK2 alpha) is classified into two subtypes CK2 alpha 1 and CK2 alpha 2. CK2 alpha 1 is a drug discovery target, whereas CK2 alpha 2 is an off-target of CK2 alpha 1 inhibitors. High amino acid sequence homology between these subtypes hampers efforts to produce ATP competitive inhibitors that are highly selective to CK2 alpha 1. Hematein was identified previously as a non-ATP-competitive inhibitor for CK2 alpha 1, whereas this compound acts as an ATP competitive CK2 alpha 2 inhibitor. Crystal structures of CK2 alpha 1 and CK2 alpha 2 in complex with hematein revealed distinct binding features that provide structural insights for producing CK2 alpha 1-selective inhibitors.
引用
收藏
页数:4
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