CoV3D: a database of high resolution coronavirus protein structures. Issue Volume 49:Issue D1(2021) (5th September 2020)

• Record Type: Journal Article
• Authors: Gowthaman, Ragul; Guest, Johnathan D; Yin, Rui; Adolf-Bryfogle, Jared; Schief, William R; Pierce, Brian G
• Is Part Of: Nucleic acids research. Volume 49:Issue D1(2021)
• Page Start: D282
• Page End: D287
• Publication Date: 2020-09-05
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gkaa731
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: SARS-CoV-2, the etiologic agent of COVID-19, exemplifies the general threat to global health posed by coronaviruses. The urgent need for effective vaccines and therapies is leading to a rapid rise in the number of high resolution structures of SARS-CoV-2 proteins that collectively reveal a map of virus vulnerabilities. To assist structure-based design of vaccines and therapeutics against SARS-CoV-2 and other coronaviruses, we have developed CoV3D, a database and resource for coronavirus protein structures, which is updated on a weekly basis. CoV3D provides users with comprehensive sets of structures of coronavirus proteins and their complexes with antibodies, receptors, and small molecules. Integrated molecular viewers allow users to visualize structures of the spike glycoprotein, which is the major target of neutralizing antibodies and vaccine design efforts, as well as sets of spike-antibody complexes, spike sequence variability, and known polymorphisms. In order to aid structure-based design and analysis of the spike glycoprotein, CoV3D permits visualization and download of spike structures with modeled N-glycosylation at known glycan sites, and contains structure-based classification of spike conformations, generated by unsupervised clustering. CoV3D can serve the research community as a centralized reference and resource for spike and other coronavirus protein structures, and is available at: https://cov3d.ibbr.umd.edu . Graphical Abstract: