Evidence map›Paper›PMID 38460782›Full record

ReviewBiochimica et biophysica acta. Biomembranes2024

Perception and protection: The role of Bce-modules in antimicrobial peptide resistance.

Benjamin J Orlando

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Biomembranes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. The extracellular domain ofFrontiers in microbiology · 2025
    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

1 author.

Benjamin J OrlandoDept. of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824, USA. Electronic address: orlandob@msu.edu.

Funding

Structural Basis of Antimicrobial Peptide Sensing and ResistanceR35GM146721 · NIGMS · MICHIGAN STATE UNIVERSITY · PI Benjamin Joseph Orlando · 2022 to 2026
$1.9M
NIGMS NIH HHS R35 GM146721
6 · The paper itself

Abstract

Continual synthesis and remodeling of the peptidoglycan layer surrounding Gram-positive cells is essential for their survival. Diverse antimicrobial peptides target the lipid intermediates involved in this process. To sense and counteract assault from antimicrobial peptides, low G + C content gram-positive bacteria (Firmicutes) have evolved membrane protein complexes known as Bce-modules. These complexes consist minimally of an ABC transporter and a two-component system that work in tandem to perceive and confer resistance against antimicrobial peptides. In this mini-review I highlight recent breakthroughs in comprehending the structure and function of these unusual membrane protein complexes, with a particular focus on the BceAB-RS system present in Bacillus subtilis.

Indexed as

Anti-Bacterial AgentsAntimicrobial PeptidesATP-Binding Cassette TransportersBacterial ProteinsDrug Resistance, BacterialPeptidesPerceptionAnti-Bacterial AgentsAntimicrobial PeptidesATP-Binding Cassette TransportersBacterial ProteinsPeptidesABC transporterAntimicrobialCryo-EMHistidine kinaseMembrane protein

Identifiers

PMID38460782
PMCPMC11009047

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.