Functional and druggability analysis of the SARS-CoV-2 proteome
- Autores
- Cavasotto, Claudio Norberto; Sánchez Lamas, Maximiliano; Maggini, Julián
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The infectious coronavirus disease (COVID-19) pandemic, caused by the coronavirus SARS-CoV-2, appeared in December 2019 in Wuhan, China, and has spread worldwide. As of today, more than 22 million people have been infected, with almost 800,000 fatalities. With the purpose of contributing to the development of effective therapeutics, this work provides an overview of the viral machinery and functional role of each SARS-CoV-2 protein, and a thorough analysis of the structure and druggability assessment of the viral proteome. All structural, non-structural, and accessory proteins of SARS-CoV-2 have been studied, and whenever experimental structural data of SARS-CoV-2 proteins were not available, homology models were built based on solved SARS-CoV structures. Several potential allosteric or protein-protein interaction druggable sites on different viral targets were identified, knowledge that could be used to expand current drug discovery endeavors beyond the cysteine proteases and the polymerase complex. It is our hope that this study will support the efforts of the scientific community both in understanding the molecular determinants of this disease and in widening the repertoire of viral targets in the quest for repurposed or novel drugs against COVID-19.
Fil: Cavasotto, Claudio Norberto. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; Argentina. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina
Fil: Sánchez Lamas, Maximiliano. Universidad Austral; Argentina
Fil: Maggini, Julián. Universidad Austral; Argentina - Materia
-
COVID-19
SARS-COV-2
PROTEOME
DRUGGABILITY - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/112903
Ver los metadatos del registro completo
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Functional and druggability analysis of the SARS-CoV-2 proteomeCavasotto, Claudio NorbertoSánchez Lamas, MaximilianoMaggini, JuliánCOVID-19SARS-COV-2PROTEOMEDRUGGABILITYhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The infectious coronavirus disease (COVID-19) pandemic, caused by the coronavirus SARS-CoV-2, appeared in December 2019 in Wuhan, China, and has spread worldwide. As of today, more than 22 million people have been infected, with almost 800,000 fatalities. With the purpose of contributing to the development of effective therapeutics, this work provides an overview of the viral machinery and functional role of each SARS-CoV-2 protein, and a thorough analysis of the structure and druggability assessment of the viral proteome. All structural, non-structural, and accessory proteins of SARS-CoV-2 have been studied, and whenever experimental structural data of SARS-CoV-2 proteins were not available, homology models were built based on solved SARS-CoV structures. Several potential allosteric or protein-protein interaction druggable sites on different viral targets were identified, knowledge that could be used to expand current drug discovery endeavors beyond the cysteine proteases and the polymerase complex. It is our hope that this study will support the efforts of the scientific community both in understanding the molecular determinants of this disease and in widening the repertoire of viral targets in the quest for repurposed or novel drugs against COVID-19.Fil: Cavasotto, Claudio Norberto. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; Argentina. Universidad Austral. Facultad de Ciencias Biomédicas; ArgentinaFil: Sánchez Lamas, Maximiliano. Universidad Austral; ArgentinaFil: Maggini, Julián. Universidad Austral; ArgentinaCold Spring Harbor Laboratory2020-08-22info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/112903Cavasotto, Claudio Norberto; Sánchez Lamas, Maximiliano; Maggini, Julián; Functional and druggability analysis of the SARS-CoV-2 proteome; Cold Spring Harbor Laboratory; bioRxiv; 2020; 22-8-2020; 1-592692-8205CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.biorxiv.org/content/10.1101/2020.08.21.261404v1info:eu-repo/semantics/altIdentifier/doi/10.1101/2020.08.21.261404info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:23:16Zoai:ri.conicet.gov.ar:11336/112903instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:23:16.728CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Functional and druggability analysis of the SARS-CoV-2 proteome |
title |
Functional and druggability analysis of the SARS-CoV-2 proteome |
spellingShingle |
Functional and druggability analysis of the SARS-CoV-2 proteome Cavasotto, Claudio Norberto COVID-19 SARS-COV-2 PROTEOME DRUGGABILITY |
title_short |
Functional and druggability analysis of the SARS-CoV-2 proteome |
title_full |
Functional and druggability analysis of the SARS-CoV-2 proteome |
title_fullStr |
Functional and druggability analysis of the SARS-CoV-2 proteome |
title_full_unstemmed |
Functional and druggability analysis of the SARS-CoV-2 proteome |
title_sort |
Functional and druggability analysis of the SARS-CoV-2 proteome |
dc.creator.none.fl_str_mv |
Cavasotto, Claudio Norberto Sánchez Lamas, Maximiliano Maggini, Julián |
author |
Cavasotto, Claudio Norberto |
author_facet |
Cavasotto, Claudio Norberto Sánchez Lamas, Maximiliano Maggini, Julián |
author_role |
author |
author2 |
Sánchez Lamas, Maximiliano Maggini, Julián |
author2_role |
author author |
dc.subject.none.fl_str_mv |
COVID-19 SARS-COV-2 PROTEOME DRUGGABILITY |
topic |
COVID-19 SARS-COV-2 PROTEOME DRUGGABILITY |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
The infectious coronavirus disease (COVID-19) pandemic, caused by the coronavirus SARS-CoV-2, appeared in December 2019 in Wuhan, China, and has spread worldwide. As of today, more than 22 million people have been infected, with almost 800,000 fatalities. With the purpose of contributing to the development of effective therapeutics, this work provides an overview of the viral machinery and functional role of each SARS-CoV-2 protein, and a thorough analysis of the structure and druggability assessment of the viral proteome. All structural, non-structural, and accessory proteins of SARS-CoV-2 have been studied, and whenever experimental structural data of SARS-CoV-2 proteins were not available, homology models were built based on solved SARS-CoV structures. Several potential allosteric or protein-protein interaction druggable sites on different viral targets were identified, knowledge that could be used to expand current drug discovery endeavors beyond the cysteine proteases and the polymerase complex. It is our hope that this study will support the efforts of the scientific community both in understanding the molecular determinants of this disease and in widening the repertoire of viral targets in the quest for repurposed or novel drugs against COVID-19. Fil: Cavasotto, Claudio Norberto. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; Argentina. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina Fil: Sánchez Lamas, Maximiliano. Universidad Austral; Argentina Fil: Maggini, Julián. Universidad Austral; Argentina |
description |
The infectious coronavirus disease (COVID-19) pandemic, caused by the coronavirus SARS-CoV-2, appeared in December 2019 in Wuhan, China, and has spread worldwide. As of today, more than 22 million people have been infected, with almost 800,000 fatalities. With the purpose of contributing to the development of effective therapeutics, this work provides an overview of the viral machinery and functional role of each SARS-CoV-2 protein, and a thorough analysis of the structure and druggability assessment of the viral proteome. All structural, non-structural, and accessory proteins of SARS-CoV-2 have been studied, and whenever experimental structural data of SARS-CoV-2 proteins were not available, homology models were built based on solved SARS-CoV structures. Several potential allosteric or protein-protein interaction druggable sites on different viral targets were identified, knowledge that could be used to expand current drug discovery endeavors beyond the cysteine proteases and the polymerase complex. It is our hope that this study will support the efforts of the scientific community both in understanding the molecular determinants of this disease and in widening the repertoire of viral targets in the quest for repurposed or novel drugs against COVID-19. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-08-22 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/112903 Cavasotto, Claudio Norberto; Sánchez Lamas, Maximiliano; Maggini, Julián; Functional and druggability analysis of the SARS-CoV-2 proteome; Cold Spring Harbor Laboratory; bioRxiv; 2020; 22-8-2020; 1-59 2692-8205 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/112903 |
identifier_str_mv |
Cavasotto, Claudio Norberto; Sánchez Lamas, Maximiliano; Maggini, Julián; Functional and druggability analysis of the SARS-CoV-2 proteome; Cold Spring Harbor Laboratory; bioRxiv; 2020; 22-8-2020; 1-59 2692-8205 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.biorxiv.org/content/10.1101/2020.08.21.261404v1 info:eu-repo/semantics/altIdentifier/doi/10.1101/2020.08.21.261404 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Cold Spring Harbor Laboratory |
publisher.none.fl_str_mv |
Cold Spring Harbor Laboratory |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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