An Update on the Current State of SARS-CoV-2 Mac1 Inhibitors
Author:
Affiliation:
1. Department of Molecular Biosciences, University of Kansas, Lawrence, KS 66045, USA
2. Department of Chemistry, McDaniel College, 2 College Hill, Westminster, MD 21157, USA
Abstract
Funder
NIH
Publisher
MDPI AG
Subject
Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy
Link
https://www.mdpi.com/2076-0817/12/10/1221/pdf
Reference34 articles.
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2. The Crystal Structure of AF1521 a Protein from Archaeoglobus Fulgidus with Homology to the Non-Histone Domain of MacroH2A;Allen;J. Mol. Biol.,2003
3. The Macro Domain Is an ADP-Ribose Binding Module;Karras;EMBO J.,2005
4. ADP-Ribosyltransferases, an Update on Function and Nomenclature;Ahel;FEBS J.,2021
5. Leung, A.K.L., McPherson, R.L., and Griffin, D.E. (2018). Macrodomain ADP-Ribosylhydrolase and the Pathogenesis of Infectious Diseases. PLoS Pathog., 14.
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2. Synthesis of Structural ADP-Ribose Analogues as Inhibitors for SARS-CoV-2 Macrodomain 1;Organic Letters;2024-06-27
3. 1-L Transcription of SARS-CoV-2 Spike Protein S1 Subunit;International Journal of Molecular Sciences;2024-04-18
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