Evidence map›Paper›PMID 42710897›Full record

ReviewOpen biology2026

Molecular basis and therapeutic potential of sortase A inhibitors as new antibiotics against MDR pathogens.

Ananya Dash, Christopher LaRock

Abstract readReview
In one paragraph

Review in Open biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ananya DashImmunology and Molecular Pathogenesis Graduate Program, Emory University , Atlanta, GA, USA.
Christopher LaRockDepartment of Microbiology and Immunology, Emory University School of Medicine , Atlanta, GA, USA.ORCID 0000-0003-3035-5331

Funding

Proteolytic regulation of the Streptococcus pyogenes cell surfaceR01AI153071 · NIAID · EMORY UNIVERSITY · PI LAROCK, CHRISTOPHER N · 2021 to 2025
$1.9M
American Heart Association Fellowship 25PRE1372818Burroughs Wellcome Fund Investigator in the Pathogenesis of Infectious Disease award (C.L.)National Institute of Allergy and Infectious Diseases of the NIH AI153071NIAID NIH HHS R01 AI153071NIH HHS
6 · The paper itself

Abstract

Attaching proteins to the cell surface presents a technical challenge to Gram-positive bacteria. A class of enzymes called sortases solves this challenge by covalently anchoring proteins, including an arsenal of virulence factors, to the cell wall. Most Gram-positive bacteria have multiple critical factors that are anchored in this manner and, coupled with the extracellular location of this reaction, make sortase an attractive target for the development of antibiotics. However, since sortase is neither essential nor itself a virulence factor, it is a very different sort of target compared to those investigated in other antibiotic strategies. This review explores the challenges of treating infection by Gram-positive pathogens, the importance of sortase-anchored proteins in the host-pathogen interaction and the known and probable antimicrobial effects of sortase inhibition for infections by Staphylococcus aureus, Streptococcus pyogenes, Bacillus anthracis, Listeria monocytogenes and other Gram-positive pathogens.

Indexed as

AminoacyltransferasesAnti-Bacterial AgentsBacterial ProteinsCysteine EndopeptidasesDrug Resistance, Multiple, BacterialEnzyme InhibitorsGram-Positive BacteriaGram-Positive Bacterial InfectionsAnimalsHost-Pathogen InteractionsHumansAminoacyltransferasesAnti-Bacterial AgentsBacterial ProteinsCysteine EndopeptidasesEnzyme Inhibitorssortase Aantibiotic discoveryanti-infectiveGram-positiveinfectious diseasesortase

Identifiers

PMID42710897
PMCPMC13561070

What Socratic 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 Socratic graph.