Literature DB >> 31859160

Structural insights for producing CK2α1-specific inhibitors.

Masato Tsuyuguchi1, Tetsuko Nakaniwa2, Akira Hirasawa3, Isao Nakanishi4, Takayoshi Kinoshita5.   

Abstract

Casein kinase 2 catalytic subunit (CK2α) is classified into two subtypes CK2α1 and CK2α2. CK2α1 is a drug discovery target, whereas CK2α2 is an off-target of CK2α1 inhibitors. High amino acid sequence homology between these subtypes hampers efforts to produce ATP competitive inhibitors that are highly selective to CK2α1. Hematein was identified previously as a non-ATP-competitive inhibitor for CK2α1, whereas this compound acts as an ATP competitive CK2α2 inhibitor. Crystal structures of CK2α1 and CK2α2 in complex with hematein revealed distinct binding features that provide structural insights for producing CK2α1-selective inhibitors.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Binding mode; CK2α1; Conformational change; Crystal structure; Selectivity

Year:  2019        PMID: 31859160     DOI: 10.1016/j.bmcl.2019.126837

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Crystal structure of Arabidopsis thaliana casein kinase 2 α1.

Authors:  Manon Demulder; Lieven De Veylder; Remy Loris
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2020-04-06       Impact factor: 1.056

  1 in total

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