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dc.contributor.authorO'Connor, Joseph J.
dc.contributor.authorFerraris, Dana
dc.contributor.authorFehr, Anthony R.
dc.date.accessioned2024-06-03T18:02:31Z
dc.date.available2024-06-03T18:02:31Z
dc.date.issued2023-10-07
dc.identifier.citationO'Connor JJ, Ferraris D, Fehr AR. An Update on the Current State of SARS-CoV-2 Mac1 Inhibitors. Pathogens. 2023 Oct 7;12(10):1221. doi: 10.3390/pathogens12101221. PMID: 37887737; PMCID: PMC10610136en_US
dc.identifier.urihttps://hdl.handle.net/1808/35090
dc.description.abstractNon-structural protein 3 (nsp3) from all coronaviruses (CoVs) contains a conserved macrodomain, known as Mac1, that has been proposed as a potential therapeutic target for CoVs due to its critical role in viral pathogenesis. Mac1 is an ADP-ribose binding protein and ADP-ribosylhydrolase that promotes replication and blocks IFN responses, though the precise mechanisms it uses to carry out these functions remain unknown. Over the past 3 years following the onset of COVID-19, several groups have used high-throughput screening with multiple assays and chemical modifications to create unique chemical inhibitors of the SARS-CoV-2 Mac1 protein. Here, we summarize the current efforts to identify selective and potent inhibitors of SARS-CoV-2 Mac1.en_US
dc.publisherMDPIen_US
dc.rightsCopyright © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.subjectCoronavirusen_US
dc.subjectSARS-CoV-2en_US
dc.subjectMacrodomainen_US
dc.subjectMac1en_US
dc.subjectADP-ribosylationen_US
dc.subjectInhibitorsen_US
dc.subjectADP-ribosylhydrolaseen_US
dc.titleAn Update on the Current State of SARS-CoV-2 Mac1 Inhibitorsen_US
dc.typeArticleen_US
kusw.kuauthorO'Connor, Joseph J.
kusw.kudepartmentDepartment of Molecular Biosciencesen_US
dc.identifier.doi10.3390/pathogens12101221en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5791-5939en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1560-1573en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC10610136en_US
dc.rights.accessrightsopenAccessen_US


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Copyright © 2023 by the authors.
Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as: Copyright © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).