Evidence map›Paper›PMID 42635430›Full record

ReviewJournal of virology2026

Dissecting the dsDNA viral packaging machinery: structural evolution and potential for therapeutics.

Makayla N Leroux, Carolyn M Teschke

Abstract readReview
In one paragraph

Review in Journal of virology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Makayla N LerouxDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut, USA.ORCID 0000-0002-0009-3628
Carolyn M TeschkeDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut, USA.ORCID 0000-0001-6420-4895

Funding

Phages as Lenses to Study Virus Assembly and Virus: Host InteractionsR35GM156358 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI CAROLYN M TESCHKE · 2025 to 2026
$1.2M
NIGMS NIH HHS R35 GM156358NIH HHS R35GM156358
6 · The paper itself

Abstract

Some double-stranded DNA viruses, such as herpesviruses and bacteriophages, utilize a powerful molecular motor to package DNA into their capsids to liquid-crystalline density. The motor is composed of large and small terminase subunits that bind to a portal complex located at a unique vertex on the icosahedral capsid. The small terminase is critical for recognition of the viral genomic DNA. The enzymatic component of the motor is the large terminase that has two functional domains necessary for ATP hydrolysis and DNA cleavage. Bacteriophage large terminase amino acid sequences are highly divergent, but their overall structural architecture and function are conserved across both tailed bacteriophages and herpesviruses. There are limited antiviral drugs for herpesvirus infections. Therefore, the viral DNA packaging motor is being investigated as an alternative drug target. In this review, we discuss the past and recent genetic, biochemical, and structural research on viral terminase motors that has illuminated their role in DNA packaging and potential as candidates for antiviral drug targeting.

Indexed as

BacteriophagesDNA PackagingDNA, ViralDNA VirusesEndodeoxyribonucleasesVirus AssemblyAntiviral AgentsCapsidHerpesviridaeHumansViral ProteinsAntiviral AgentsDNA, ViralEndodeoxyribonucleasesterminaseViral ProteinsDNA packaginglarge terminasemolecular motor

Identifiers

PMID42635430
PMCPMC13595956

What OpenQuestion holds

Textmetadata
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.