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Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase

[Image: see text] Transmissible and infectious viruses can cause large-scale epidemics around the world. This is because the virus can constantly mutate and produce different variants and subvariants to counter existing treatments. Therefore, a variety of treatments are urgently needed to keep up wi...

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Autores principales: Hao, Yixuan, Chen, Maozi, Othman, Yasmin, Xie, Xiang-Qun, Feng, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609052/
https://www.ncbi.nlm.nih.gov/pubmed/36312370
http://dx.doi.org/10.1021/acsomega.2c04258
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author Hao, Yixuan
Chen, Maozi
Othman, Yasmin
Xie, Xiang-Qun
Feng, Zhiwei
author_facet Hao, Yixuan
Chen, Maozi
Othman, Yasmin
Xie, Xiang-Qun
Feng, Zhiwei
author_sort Hao, Yixuan
collection PubMed
description [Image: see text] Transmissible and infectious viruses can cause large-scale epidemics around the world. This is because the virus can constantly mutate and produce different variants and subvariants to counter existing treatments. Therefore, a variety of treatments are urgently needed to keep up with the mutation of the viruses. To facilitate the research of such treatment, we updated our Virus-CKB 1.0 to Virus-CKB 2.0, which contains 10 kinds of viruses, including enterovirus, dengue virus, hepatitis C virus, Zika virus, herpes simplex virus, Andes orthohantavirus, human immunodeficiency virus, Ebola virus, Lassa virus, influenza virus, coronavirus, and norovirus. To date, Virus-CKB 2.0 archived at least 65 antiviral drugs (such as remdesivir, telaprevir, acyclovir, boceprevir, and nelfinavir) in the market, 178 viral-related targets with 292 available 3D crystal or cryo-EM structures, and 3766 chemical agents reported for these target proteins. Virus-CKB 2.0 is integrated with established tools for target prediction and result visualization; these include HTDocking, TargetHunter, blood–brain barrier (BBB) predictor, Spider Plot, etc. The Virus-CKB 2.0 server is accessible at https://www.cbligand.org/g/virus-ckb. By using the established chemogenomic tools and algorithms and newly developed tools, we can screen FDA-approved drugs and chemical compounds that may bind to these proteins involved in viral-associated disease regulation. If the virus strain mutates and the vaccine loses its effect, we can still screen drugs that can be used to treat the mutated virus in a fleeting time. In some cases, we can even repurpose FDA-approved drugs through Virus-CKB 2.0.
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spelling pubmed-96090522022-10-28 Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase Hao, Yixuan Chen, Maozi Othman, Yasmin Xie, Xiang-Qun Feng, Zhiwei ACS Omega [Image: see text] Transmissible and infectious viruses can cause large-scale epidemics around the world. This is because the virus can constantly mutate and produce different variants and subvariants to counter existing treatments. Therefore, a variety of treatments are urgently needed to keep up with the mutation of the viruses. To facilitate the research of such treatment, we updated our Virus-CKB 1.0 to Virus-CKB 2.0, which contains 10 kinds of viruses, including enterovirus, dengue virus, hepatitis C virus, Zika virus, herpes simplex virus, Andes orthohantavirus, human immunodeficiency virus, Ebola virus, Lassa virus, influenza virus, coronavirus, and norovirus. To date, Virus-CKB 2.0 archived at least 65 antiviral drugs (such as remdesivir, telaprevir, acyclovir, boceprevir, and nelfinavir) in the market, 178 viral-related targets with 292 available 3D crystal or cryo-EM structures, and 3766 chemical agents reported for these target proteins. Virus-CKB 2.0 is integrated with established tools for target prediction and result visualization; these include HTDocking, TargetHunter, blood–brain barrier (BBB) predictor, Spider Plot, etc. The Virus-CKB 2.0 server is accessible at https://www.cbligand.org/g/virus-ckb. By using the established chemogenomic tools and algorithms and newly developed tools, we can screen FDA-approved drugs and chemical compounds that may bind to these proteins involved in viral-associated disease regulation. If the virus strain mutates and the vaccine loses its effect, we can still screen drugs that can be used to treat the mutated virus in a fleeting time. In some cases, we can even repurpose FDA-approved drugs through Virus-CKB 2.0. American Chemical Society 2022-10-10 /pmc/articles/PMC9609052/ /pubmed/36312370 http://dx.doi.org/10.1021/acsomega.2c04258 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Hao, Yixuan
Chen, Maozi
Othman, Yasmin
Xie, Xiang-Qun
Feng, Zhiwei
Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase
title Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase
title_full Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase
title_fullStr Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase
title_full_unstemmed Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase
title_short Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase
title_sort virus-ckb 2.0: viral-associated disease-specific chemogenomics knowledgebase
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609052/
https://www.ncbi.nlm.nih.gov/pubmed/36312370
http://dx.doi.org/10.1021/acsomega.2c04258
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