Discovery of a CK2α′-Biased ATP-Competitive Inhibitor from a High-Throughput Screen of an Allosteric-Inhibitor-Like Compound Library-Reference-Cited by-同舟云学术

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Discovery of a CK2α′-Biased ATP-Competitive Inhibitor from a High-Throughput Screen of an Allosteric-Inhibitor-Like Compound Library

Published:2024-06-22 Issue:15 Volume:15 Page:2703-2718
ISSN:1948-7193
Container-title:ACS Chemical Neuroscience
language:en
Short-container-title:ACS Chem. Neurosci.

Author:

Mudaliar Deepti¹,Mansky Rachel H.²,White Angel²,Baudhuin Grace²,Hawkinson Jon^ORCID,Wong Henry¹^ORCID,Walters Michael A.¹^ORCID,Gomez-Pastor Rocio²^ORCID

Affiliation:

1. Department of Medicinal Chemistry, Institute for Therapeutics Discovery and Development, University of Minnesota, Minneapolis, Minnesota 55414, United States

2. Department of Neuroscience, School of Medicine, University of Minnesota, Minneapolis, Minnesota 55414, United States

Funder

National Institute of Neurological Disorders and Stroke

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acschemneuro.4c00062

Reference96 articles.

1. THE ENZYMATIC PHOSPHORYLATION OF PROTEINS

2. Protein kinase CK2: structure, regulation and role in cellular decisions of life and death

3. Protein Kinase CK2 is a Constitutively Active Enzyme that Promotes Cell Survival: Strategies to Identify CK2 Substrates and Manipulate its Activity in Mammalian Cells

4. The Global Phosphorylation Landscape of SARS-CoV-2 Infection

5. CK2—An Emerging Target for Neurological and Psychiatric Disorders

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