Evidence map›Paper›PMID 37115000›Full record

ArticleNucleic acids research2023

Allosteric regulation and crystallographic fragment screening of SARS-CoV-2 NSP15 endoribonuclease.

Andre Schutzer Godoy, Aline Minalli Nakamura, Alice Douangamath, Yun Song, Gabriela Dias Noske, Victor Oliveira Gawriljuk, Rafaela Sachetto Fernandes, Humberto D Muniz Pereira, Ketllyn Irene Zagato Oliveira, Daren Fearon and 14 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
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  9. Synthesis, HScientific reports · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. SARS-CoV-2 nsp15 endoribonuclease antagonizes dsRNA-induced antiviral signaling.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Inhibition of SARS-CoV-2 NSP-15 by Uridine-5'-Monophosphate Analogues Using QSAR Modelling, Molecular Dynamics Simulations, and Free Energy Landscape.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Article
  15. Article
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

24 authors at 7 institutions in 5 countries.

Andre Schutzer GodoySao Carlos Institute of Physics, University of Sao Paulo, Av. Joao Dagnone, 1100 - Jardim Santa Angelina, Sao Carlos, 13563-120, Brazil.ORCID 0000-0002-0613-9164
Aline Minalli NakamuraSao Carlos Institute of Physics, University of Sao Paulo, Av. Joao Dagnone, 1100 - Jardim Santa Angelina, Sao Carlos, 13563-120, Brazil.
Alice DouangamathDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.
Yun SongElectron Bio-imaging Centre, Diamond Light Source Ltd., Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.
Gabriela Dias NoskeSao Carlos Institute of Physics, University of Sao Paulo, Av. Joao Dagnone, 1100 - Jardim Santa Angelina, Sao Carlos, 13563-120, Brazil.
Victor Oliveira GawriljukSao Carlos Institute of Physics, University of Sao Paulo, Av. Joao Dagnone, 1100 - Jardim Santa Angelina, Sao Carlos, 13563-120, Brazil.
Rafaela Sachetto FernandesSao Carlos Institute of Physics, University of Sao Paulo, Av. Joao Dagnone, 1100 - Jardim Santa Angelina, Sao Carlos, 13563-120, Brazil.
Humberto D Muniz PereiraSao Carlos Institute of Physics, University of Sao Paulo, Av. Joao Dagnone, 1100 - Jardim Santa Angelina, Sao Carlos, 13563-120, Brazil.
Ketllyn Irene Zagato OliveiraSao Carlos Institute of Physics, University of Sao Paulo, Av. Joao Dagnone, 1100 - Jardim Santa Angelina, Sao Carlos, 13563-120, Brazil.
Daren FearonDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.
Alexandre DiasDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.
Tobias KrojerBioMAX, MAX IV Laboratory, Fotongatan 2, Lund 224 84, Sweden.
Michael FairheadCentre for Medicines Discovery, Oxford University, Oxford OX1 3QU, UK.
Alisa PowellDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.
Louise DunnetDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.
Jose Brandao-NetoDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.
Rachael SkynerDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.
Rod ChalkCentre for Medicines Discovery, Oxford University, Oxford OX1 3QU, UK.
Dávid BajuszMedicinal Chemistry Research Group, Research Centre for Natural Sciences, Magyar tudósok krt. 2, 1117 Budapest, Hungary.ORCID 0000-0003-4277-9481
Miklós BegeDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, 4032 Debrecen, Hungary.
Anikó BorbásDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, 4032 Debrecen, Hungary.
György Miklós KeserűMedicinal Chemistry Research Group, Research Centre for Natural Sciences, Magyar tudósok krt. 2, 1117 Budapest, Hungary.
Frank von DelftDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot OX11 0QX, UK.ORCID 0000-0003-0378-0017
Glaucius OlivaSao Carlos Institute of Physics, University of Sao Paulo, Av. Joao Dagnone, 1100 - Jardim Santa Angelina, Sao Carlos, 13563-120, Brazil.
Diamond Light Source · GBUniversidade de São Paulo · BRHUN-REN Research Centre for Natural Sciences · HUUniversity of Debrecen · HUUniversity of Oxford · GBMAX IV Laboratory · SEUniversity of Johannesburg · ZA

Funding

Target enablementU19AI171399 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI CHODERA, JOHN DAMON, LEE, ALPHA ALBERT · 2022 to 2025
$89.8M
NIAID NIH HHS U19 AI171399Wellcome Trust
6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019 (COVID-19). The NSP15 endoribonuclease enzyme, known as NendoU, is highly conserved and plays a critical role in the ability of the virus to evade the immune system. NendoU is a promising target for the development of new antiviral drugs. However, the complexity of the enzyme's structure and kinetics, along with the broad range of recognition sequences and lack of structural complexes, hampers the development of inhibitors. Here, we performed enzymatic characterization of NendoU in its monomeric and hexameric form, showing that hexamers are allosteric enzymes with a positive cooperative index, and with no influence of manganese on enzymatic activity. Through combining cryo-electron microscopy at different pHs, X-ray crystallography and biochemical and structural analysis, we showed that NendoU can shift between open and closed forms, which probably correspond to active and inactive states, respectively. We also explored the possibility of NendoU assembling into larger supramolecular structures and proposed a mechanism for allosteric regulation. In addition, we conducted a large fragment screening campaign against NendoU and identified several new allosteric sites that could be targeted for the development of new inhibitors. Overall, our findings provide insights into the complex structure and function of NendoU and offer new opportunities for the development of inhibitors.

Indexed as

SARS-CoV-2Allosteric RegulationAmino Acid SequenceCOVID-19Cryoelectron MicroscopyEndoribonucleasesHumansViral Nonstructural ProteinsEndoribonucleasesnidoviral uridylate-specific endoribonucleaseViral Nonstructural Proteins

Identifiers

PMID37115000
PMCPMC10250223
OpenAlexW4367319232

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.