Evidence map›Paper›PMID 39207823›Full record

ArticleBiochemistry2024

Whole Cell Luminescence-Based Screen for Inhibitors of the Bacterial Sec Machinery.

Tia Salter, Ian Collinson, William J Allen

Abstract read
In one paragraph

Article in Biochemistry, 2024. 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

3 authors.

Tia SalterSchool of Biochemistry, University of Bristol, University Walk, Bristol BS8 1TD, United Kingdom.
Ian CollinsonSchool of Biochemistry, University of Bristol, University Walk, Bristol BS8 1TD, United Kingdom.ORCID 0000-0002-3931-0503
William J AllenSchool of Biochemistry, University of Bristol, University Walk, Bristol BS8 1TD, United Kingdom.

Funding

Wellcome Trust 209739
6 · The paper itself

Abstract

There is a pressing need for new antibiotics to combat rising resistance to those already in use. The bacterial general secretion (Sec) system has long been considered a good target for novel antimicrobials thanks to its irreplacable role in maintaining cell envelope integrity, yet the lack of a robust, high-throughput method to screen for Sec inhibition has so far hampered efforts to realize this potential. Here, we have adapted our recently developed

Indexed as

Anti-Bacterial AgentsHigh-Throughput Screening AssaysBacterial ProteinsEscherichia coliLuminescenceLuminescent MeasurementsSEC Translocation ChannelsAnti-Bacterial AgentsBacterial ProteinsSEC Translocation Channels

Identifiers

PMID39207823
PMCPMC11411707

What Socratic 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 Socratic graph.