Evidence map›Paper›PMID 32945615›Full record

ReviewMolecular oral microbiology2021

The enterococcal PASTA kinase: A sentinel for cell envelope stress.

Dušanka Djorić, Nicole E Minton, Christopher J Kristich

Open access · greenAbstract readReview
In one paragraph

Review in Molecular oral microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Maintenance of heme homeostasis inJournal of bacteriology · 2023
    Article
  5. Conformational changes in the activation loop of a bacterial PASTA kinase.Protein science : a publication of the Protein Society · 2023
    Article
  6. Article
  7. Article
  8. Integrative structural biology of the penicillin-binding protein-1 fromComputational and structural biotechnology journal · 2021
    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

3 authors at 1 institution in 1 country.

Dušanka DjorićDepartment of Microbiology and Immunology, Center for Infectious Disease Research, Medical College of Wisconsin, Milwaukee, WI, USA.
Nicole E MintonDepartment of Microbiology and Immunology, Center for Infectious Disease Research, Medical College of Wisconsin, Milwaukee, WI, USA.
Christopher J KristichDepartment of Microbiology and Immunology, Center for Infectious Disease Research, Medical College of Wisconsin, Milwaukee, WI, USA.ORCID 0000-0002-1660-0006
Medical College of Wisconsin · US

Funding

Intrinsic cephalosporin resistance in enterococciR01AI134660 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI KRISTICH, CHRISTOPHER J · 2018 to 2021
$1.5M
Conformation and functional dynamics of a bacterial PASTA kinaseR01GM135256 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI KRISTICH, CHRISTOPHER J · 2020 to 2023
$1.4M
Role of a cell wall assembly factor in enterococcal antimicrobial resistanceR21AI128219 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI KRISTICH, CHRISTOPHER J · 2017 to 2018
$424k
Genes of unknown function impacting antimicrobial resistance in enterococciR21AI132927 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI KRISTICH, CHRISTOPHER J · 2017 to 2018
$424k
NIAID NIH HHS R01 AI134660NIAID NIH HHS R21 AI128219NIAID NIH HHS R21 AI132927NIGMS NIH HHS R01 GM135256
6 · The paper itself

Abstract

Enterococci are Gram-positive, opportunistic pathogens that reside throughout the gastrointestinal tracts of most terrestrial organisms. Enterococci are resistant to many antibiotics, which makes enterococcal infections difficult to treat. Enterococci are also particularly hardy bacteria that can tolerate a variety of environmental stressors. Understanding how enterococci sense and respond to the extracellular environment to enact adaptive biological responses may identify new targets that can be exploited for development of treatments for enterococcal infections. Bacterial eukaryotic-like serine/threonine kinases (eSTKs) and cognate phosphatases (STPs) are important signaling systems that mediate biological responses to extracellular stimuli. Some bacterial eSTKs are transmembrane proteins that contain a series of extracellular repeats of the penicillin-binding and Ser/Thr kinase-associated (PASTA) domain, leading to their designation as "PASTA kinases." Enterococcal genomes encode a single PASTA kinase and its cognate phosphatase. Investigations of the enterococcal PASTA kinase revealed its importance in resistance to antibiotics and other cell wall stresses, in enterococcal colonization of the mammalian gut, clues about its mechanism of signal transduction, and its integration with other enterococcal signal transduction systems. In this review, we describe the current state of knowledge of PASTA kinase signaling in enterococci and describe important gaps that still need to be addressed to provide a better understanding of this important signaling system.

Indexed as

Cell WallProtein Serine-Threonine KinasesAnimalsAnti-Bacterial AgentsCell MembraneEnterococcus faecalisSignal TransductionAnti-Bacterial AgentsProtein Serine-Threonine Kinasescell wall stressenterococcusPASTA kinasesignal transduction

Identifiers

PMID32945615
PMCPMC7969467
OpenAlexW3087564697

What OpenQuestion holds

Textmetadata
LicenceTDM
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.