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 50 条
  • [41] Proposed Allosteric Inhibitors Bind to the ATP Site of CK2α
    Brear, Paul
    Ball, Darby
    Stott, Katherine
    D'Arcy, Sheena
    Hyvonen, Marko
    JOURNAL OF MEDICINAL CHEMISTRY, 2020, 63 (21) : 12786 - 12798
  • [42] Antitumoral activity of allosteric inhibitors of protein kinase CK2
    Moucadel, Virginie
    Prudent, Renaud
    Sautel, Celine F.
    Teillet, Florence
    Barette, Caroline
    Lafanechere, Laurence
    Receveur-Brechot, Veronique
    Cochet, Claude
    ONCOTARGET, 2011, 2 (12) : 997 - 1010
  • [43] Novel potent and selective inhibitors of protein kinase CK2
    Prudent, R.
    Moucadel, V
    Laudet, B.
    Cochet, C.
    BULLETIN DU CANCER, 2008, 95 : S66 - S66
  • [44] Salicylaldehyde derivatives as new protein kinase CK2 inhibitors
    Prudent, Renaud
    Lopez-Ramos, Miriam
    Moucadel, Virginie
    Barette, Caroline
    Grierson, David
    Mouawad, Liliane
    Florent, Jean-Claude
    Lafanechere, Laurence
    Schmidt, Frederic
    Cochet, Claude
    BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2008, 1780 (12): : 1412 - 1420
  • [45] Synthesis and medicinal chemistry optimization of CK2 kinase inhibitors
    Dowling, James
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 251
  • [46] Cell-permeable dual inhibitors of protein kinases CK2 and PIM-1: structural features and pharmacological potential
    Giorgio Cozza
    Cristina Girardi
    Alessandro Ranchio
    Graziano Lolli
    Stefania Sarno
    Andrzej Orzeszko
    Zygmunt Kazimierczuk
    Roberto Battistutta
    Maria Ruzzene
    Lorenzo A. Pinna
    Cellular and Molecular Life Sciences, 2014, 71 : 3173 - 3185
  • [47] Cell-permeable dual inhibitors of protein kinases CK2 and PIM-1: structural features and pharmacological potential
    Cozza, Giorgio
    Girardi, Cristina
    Ranchio, Alessandro
    Lolli, Graziano
    Sarno, Stefania
    Orzeszko, Andrzej
    Kazimierczuk, Zygmunt
    Battistutta, Roberto
    Ruzzene, Maria
    Pinna, Lorenzo A.
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2014, 71 (16) : 3173 - 3185
  • [48] Structural Determinants of CX-4945 Derivatives as Protein Kinase CK2 Inhibitors: A Computational Study
    Liu, Hongbo
    Wang, Xia
    Wang, Jian
    Wang, Jinghui
    Li, Yan
    Yang, Ling
    Li, Guohui
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2011, 12 (10): : 7004 - 7021
  • [49] Re-evaluation of protein kinase CK2 pleiotropy: new insights provided by a phosphoproteomics analysis of CK2 knockout cells
    Franchin, Cinzia
    Borgo, Christian
    Cesaro, Luca
    Zaramella, Silvia
    Vilardell, Jordi
    Salvi, Mauro
    Arrigoni, Giorgio
    Pinna, Lorenzo A.
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2018, 75 (11) : 2011 - 2026
  • [50] Structure-Based Design Of Novel Potent Protein Kinase CK2 (CK2) Inhibitors with Phenyl-azole Scaffolds
    Hou, Zengye
    Nakanishi, Isao
    Kinoshita, Takayoshi
    Takei, Yoshinori
    Yasue, Misato
    Misu, Ryosuke
    Suzuki, Yamato
    Nakamura, Shinya
    Kure, Tatsuhide
    Ohno, Hiroald
    Murata, Katsumi
    Kitaura, Kazuo
    Hirasawa, Akira
    Tsujimoto, Gozoh
    Oishi, Shinya
    Fujii, Nobutaka
    JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (06) : 2899 - 2903