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Modeling SARS-CoV-2 proteins in the CASP-commons experiment.
Kryshtafovych, Andriy; Moult, John; Billings, Wendy M; Della Corte, Dennis; Fidelis, Krzysztof; Kwon, Sohee; Olechnovic, Kliment; Seok, Chaok; Venclovas, Ceslovas; Won, Jonghun.
  • Kryshtafovych A; Genome Center, University of California, Davis, Davis, California, USA.
  • Moult J; Department of Cell Biology and Molecular genetics, Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, Maryland, USA.
  • Billings WM; Department of Physics & Astronomy, Brigham Young University, Provo, Utah, USA.
  • Della Corte D; Department of Physics & Astronomy, Brigham Young University, Provo, Utah, USA.
  • Fidelis K; Genome Center, University of California, Davis, Davis, California, USA.
  • Kwon S; Department of Chemistry, Seoul National University, Seoul, South Korea.
  • Olechnovic K; Institute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
  • Seok C; Department of Chemistry, Seoul National University, Seoul, South Korea.
  • Venclovas C; Institute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
  • Won J; Department of Chemistry, Seoul National University, Seoul, South Korea.
Proteins ; 89(12): 1987-1996, 2021 12.
Article in English | MEDLINE | ID: covidwho-1449944
ABSTRACT
Critical Assessment of Structure Prediction (CASP) is an organization aimed at advancing the state of the art in computing protein structure from sequence. In the spring of 2020, CASP launched a community project to compute the structures of the most structurally challenging proteins coded for in the SARS-CoV-2 genome. Forty-seven research groups submitted over 3000 three-dimensional models and 700 sets of accuracy estimates on 10 proteins. The resulting models were released to the public. CASP community members also worked together to provide estimates of local and global accuracy and identify structure-based domain boundaries for some proteins. Subsequently, two of these structures (ORF3a and ORF8) have been solved experimentally, allowing assessment of both model quality and the accuracy estimates. Models from the AlphaFold2 group were found to have good agreement with the experimental structures, with main chain GDT_TS accuracy scores ranging from 63 (a correct topology) to 87 (competitive with experiment).
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Proteins / SARS-CoV-2 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Proteins Journal subject: Biochemistry Year: 2021 Document Type: Article Affiliation country: Prot.26231

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Proteins / SARS-CoV-2 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Proteins Journal subject: Biochemistry Year: 2021 Document Type: Article Affiliation country: Prot.26231