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
相关论文
共 26 条
  • [1] PHENIX: a comprehensive Python']Python-based system for macromolecular structure solution
    Adams, Paul D.
    Afonine, Pavel V.
    Bunkoczi, Gabor
    Chen, Vincent B.
    Davis, Ian W.
    Echols, Nathaniel
    Headd, Jeffrey J.
    Hung, Li-Wei
    Kapral, Gary J.
    Grosse-Kunstleve, Ralf W.
    McCoy, Airlie J.
    Moriarty, Nigel W.
    Oeffner, Robert
    Read, Randy J.
    Richardson, David C.
    Richardson, Jane S.
    Terwilliger, Thomas C.
    Zwart, Peter H.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2010, 66 : 213 - 221
  • [2] A fragment-based approach leading to the discovery of a novel binding site and the selective CK2 inhibitor CAM4066
    De Fusco, Claudia
    Brear, Paul
    Iegre, Jessica
    Georgiou, Kathy Hadje
    Sore, Hannah F.
    Hyvonen, Marko
    Spring, David R.
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2017, 25 (13) : 3471 - 3482
  • [3] CK2 and its role in Wnt and NF-κB signaling: Linking development and cancer
    Dominguez, I.
    Sonenshein, G. E.
    Seldin, D. C.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2009, 66 (11-12) : 1850 - 1857
  • [4] Features and development of Coot
    Emsley, P.
    Lohkamp, B.
    Scott, W. G.
    Cowtan, K.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2010, 66 : 486 - 501
  • [5] Identification of hematein as a novel inhibitor of protein kinase CK2 from a natural product library
    Hung, Ming-Szu
    Xu, Zhidong
    Lin, Yu-Ching
    Mao, Jian-Hua
    Yang, Cheng-Ta
    Chang, Pey-Jium
    Jablons, David M.
    You, Liang
    [J]. BMC CANCER, 2009, 9
  • [6] XDS
    Kabsch, Wolfgang
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2010, 66 : 125 - 132
  • [7] The pp60c-Sr inhibitor PP1 is non-competitive against ATP
    Karni, R
    Mizrachi, S
    Reiss-Sklan, E
    Gazit, A
    Livnah, O
    Levitzki, A
    [J]. FEBS LETTERS, 2003, 537 (1-3) : 47 - 52
  • [8] Crystal structure of human CK2α at 1.06 Å resolution
    Kinoshita, Takayoshi
    Nakaniwa, Tetsuko
    Sekiguchi, Yusuke
    Sogabe, Yuri
    Sakurai, Atsushi
    Nakamura, Shinya
    Nakanishi, Isao
    [J]. JOURNAL OF SYNCHROTRON RADIATION, 2013, 20 : 974 - 979
  • [9] Phaser crystallographic software
    McCoy, Airlie J.
    Grosse-Kunstleve, Ralf W.
    Adams, Paul D.
    Winn, Martyn D.
    Storoni, Laurent C.
    Read, Randy J.
    [J]. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2007, 40 : 658 - 674
  • [10] One-thousand-and-one substrates of protein kinase CK2?
    Meggio, F
    Pinna, LA
    [J]. FASEB JOURNAL, 2003, 17 (03) : 349 - 368