Evidence map›Paper›PMID 38047713›Full record

ArticleJournal of virology2023

Differential inhibition of intra- and inter-molecular protease cleavages by antiviral compounds.

Jennifer S Doherty, Karla Kirkegaard

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

2 authors at 1 institution in 1 country.

Jennifer S DohertyDepartment of Genetics, Stanford University, Palo Alto, California, USA.ORCID 0000-0002-3284-4297
Karla KirkegaardDepartment of Genetics, Stanford University, Palo Alto, California, USA.ORCID 0000-0001-7628-3770
Palo Alto University · US

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 AI171399
6 · The paper itself

Abstract

importanceMost protease-targeted antiviral development evaluates the ability of small molecules to inhibit the cleavage of artificial substrates. However, before they can cleave any other substrates, viral proteases need to cleave themselves out of the viral polyprotein in which they have been translated. This can occur either intra- or inter-molecularly. Whether this process occurs intra- or inter-molecularly has implications for the potential for precursors to accumulate and for the effectiveness of antiviral drugs. We argue that evaluating candidate antivirals for their ability to block these cleavages is vital to drug development because the buildup of uncleaved precursors can be inhibitory to the virus and potentially suppress the selection of drug-resistant variants.

Indexed as

Antiviral AgentsEnterovirusViral Protease InhibitorsViral ProteasesPolyproteinsProteolysisAntiviral AgentsPolyproteinsViral Protease InhibitorsViral Proteasesantiviraldrug resistanceenterovirus A71enterovirus D68picornaviruspolioviruspolyproteinpositive-stranded RNA virusproteaseviral genetics

Identifiers

PMID38047713
PMCPMC10734437
OpenAlexW4389298853

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.