Evidence map›Paper›PMID 33392924›Full record

ArticleBiomolecular NMR assignments2021

Backbone chemical shift assignments for the SARS-CoV-2 non-structural protein Nsp9: intermediate (ms - μs) dynamics in the C-terminal helix at the dimer interface.

Garry W Buchko, Mowei Zhou, Justin K Craig, Wesley C Van Voorhis, Peter J Myler

Abstract read
In one paragraph

Article in Biomolecular NMR assignments, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Garry W BuchkoSeattle Structural Genomics Center for Infectious Disease, Seattle, USA. garry.buchko@pnnl.gov.ORCID http://orcid.org/0000-0002-3639-1061
Mowei ZhouEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.
Justin K CraigSeattle Structural Genomics Center for Infectious Disease, Seattle, USA.
Wesley C Van VoorhisSeattle Structural Genomics Center for Infectious Disease, Seattle, USA.
Peter J MylerSeattle Structural Genomics Center for Infectious Disease, Seattle, USA.

Funding

NIAID NIH HHS HHSN272201700059C
6 · The paper itself

Abstract

The Betacoronavirus SARS-CoV-2 non-structural protein Nsp9 is a 113-residue protein that is essential for viral replication, and consequently, a potential target for the development of therapeutics against COVID19 infections. To capture insights into the dynamics of the protein's backbone in solution and accelerate the identification and mapping of ligand-binding surfaces through chemical shift perturbation studies, the backbone

Indexed as

Magnetic Resonance SpectroscopyBinding SitesCarbon IsotopesCodonCrystallography, X-RayDimerizationDisulfidesHydrogenHydrogen-Ion ConcentrationKineticsLigandsNitrogen IsotopesProtein BindingProtein DomainsProtein Structure, SecondaryRNA-Binding ProteinsCarbon-13Carbon IsotopesCodonDisulfidesHydrogenLigandsNitrogen-15Nitrogen IsotopesORF1ab polyprotein, SARS-CoV-2RNA-Binding ProteinsViral Nonstructural ProteinsNative mass spectrometryNon-structural proteinProtein dynamicsSARS-CoV-2Solution NMRViral replication

Identifiers

PMID33392924
PMCPMC7779335

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.