Evidence map›Paper›PMID 32900806›Full record

ArticlemBio2020

Unstable Mechanisms of Resistance to Inhibitors of Escherichia coli Lipoprotein Signal Peptidase.

Homer Pantua, Elizabeth Skippington, Marie-Gabrielle Braun, Cameron L Noland, Jingyu Diao, Yutian Peng, Susan L Gloor, Donghong Yan, Jing Kang, Anand Kumar Katakam and 12 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 22 citations in OpenAlex.

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  19. Deletion of a previously uncharacterized lipoprotein lirL confers resistance to an inhibitor of type II signal peptidase inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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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

22 authors.

Homer Pantua *Department of Infectious Diseases, Genentech, South San Francisco, California, USA pantua.homer@gene.com kapadia.sharookh@gene.com.
Elizabeth Skippington *Department of OMNI Bioinformatics, Genentech, South San Francisco, California, USA.
Marie-Gabrielle BraunDepartment of Chemistry, Genentech, South San Francisco, California, USA.
Cameron L NolandDepartment of Structural Biology, Genentech, South San Francisco, California, USA.
Jingyu DiaoDepartment of Infectious Diseases, Genentech, South San Francisco, California, USA.
Yutian PengDepartment of Infectious Diseases, Genentech, South San Francisco, California, USA.
Susan L GloorDepartment of Biochemical and Cellular Pharmacology, Genentech, South San Francisco, California, USA.
Donghong YanDepartment of Translational Immunology, Genentech, South San Francisco, California, USA.
Jing KangDepartment of Translational Immunology, Genentech, South San Francisco, California, USA.
Anand Kumar KatakamDepartment of OMNI Bioinformatics, Genentech, South San Francisco, California, USA.
Janina ReederDepartment of OMNI Bioinformatics, Genentech, South San Francisco, California, USA.
Georgette M CastanedoDepartment of Chemistry, Genentech, South San Francisco, California, USA.
Keira GarlandDepartment of Chemistry, Genentech, South San Francisco, California, USA.
Laszlo KomuvesDepartment of OMNI Bioinformatics, Genentech, South San Francisco, California, USA.
Meredith SagollaDepartment of OMNI Bioinformatics, Genentech, South San Francisco, California, USA.
Cary D AustinDepartment of OMNI Bioinformatics, Genentech, South San Francisco, California, USA.
Jeremy MurrayDepartment of Structural Biology, Genentech, South San Francisco, California, USA.
Yiming XuDepartment of Biochemical and Cellular Pharmacology, Genentech, South San Francisco, California, USA.
Zora ModrusanDepartment of Molecular Biology, Genentech, South San Francisco, California, USA.
Min XuDepartment of Translational Immunology, Genentech, South San Francisco, California, USA.
Emily J HananDepartment of Chemistry, Genentech, South San Francisco, California, USA.
Sharookh B KapadiaDepartment of Infectious Diseases, Genentech, South San Francisco, California, USA pantua.homer@gene.com kapadia.sharookh@gene.com.ORCID 0000-0002-6301-3111

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical development of antibiotics with novel mechanisms of action to kill pathogenic bacteria is challenging, in part, due to the inevitable emergence of resistance. A phenomenon of potential clinical importance that is broadly overlooked in preclinical development is heteroresistance, an often-unstable phenotype in which subpopulations of bacterial cells show decreased antibiotic susceptibility relative to the dominant population. Here, we describe a new globomycin analog, G0790, with potent activity against the

Indexed as

AnimalsAnti-Bacterial AgentsAspartic Acid EndopeptidasesBacterial ProteinsDrug Resistance, BacterialEnterobacteriaceaeEscherichia coliEscherichia coli InfectionsFemaleHumansLipoproteinsMiceMice, Inbred C57BLPeptidesUropathogenic Escherichia coliAnti-Bacterial AgentsAspartic Acid EndopeptidasesBacterial ProteinsglobomycinLipoproteinsPeptidessignal peptidase IIglobomycinheteroresistancelipoproteinLppLspA

Identifiers

PMID32900806
PMCPMC7482066
OpenAlexW3084045401

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.