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DBCOVP: A database of coronavirus virulent glycoproteins

Since the emergence of SARS‐CoV-1 (2002), novel coronaviruses have emerged periodically like the MERS‐ CoV (2012) and now, the SARS‐CoV-2 outbreak which has posed a global threat to public health. Although, this is the third zoonotic coronavirus breakout within the last two decades, there are only a...

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Detalles Bibliográficos
Autores principales: Sahoo, Susrita, Mahapatra, Soumya Ranjan, Parida, Bikram Kumar, Rath, Satyajit, Dehury, Budheswar, Raina, Vishakha, Mohakud, Nirmal Kumar, Misra, Namrata, Suar, Mrutyunjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7679231/
https://www.ncbi.nlm.nih.gov/pubmed/33276297
http://dx.doi.org/10.1016/j.compbiomed.2020.104131
Descripción
Sumario:Since the emergence of SARS‐CoV-1 (2002), novel coronaviruses have emerged periodically like the MERS‐ CoV (2012) and now, the SARS‐CoV-2 outbreak which has posed a global threat to public health. Although, this is the third zoonotic coronavirus breakout within the last two decades, there are only a few platforms that provide information about coronavirus genomes. None of them is specific for the virulence glycoproteins and complete sequence-structural features of these virulence factors across the betacoronavirus family including SARS-CoV-2 strains are lacking. Against this backdrop, we present DBCOVP (http://covp.immt.res.in/), the first manually-curated, web-based resource to provide extensive information on the complete repertoire of structural virulent glycoproteins from coronavirus genomes belonging to betacoronavirus genera. The database provides various sequence-structural properties in which users can browse and analyze information in different ways. Furthermore, many conserved T-cell and B-cell epitopes predicted for each protein are present that may perform a significant role in eliciting the humoral and cellular immune response. The tertiary structure of the epitopes together with the docked epitope-HLA binding-complex is made available to facilitate further analysis. DBCOVP presents an easy-to-use interface with in-built tools for similarity search, cross-genome comparison, phylogenetic, and multiple sequence alignment. DBCOVP will certainly be an important resource for experimental biologists engaged in coronavirus research studies and will aid in vaccine development.