Evidence map›Paper›PMID 40221051›Full record

ReviewBiochimica et biophysica acta. Molecular cell research2025

The versatile role of YidC in membrane protein biosynthesis and quality control.

Mehmet Caliseki, Christiane Schaffitzel, Burak Veli Kabasakal

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Molecular cell research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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.

Mehmet CalisekiTurkish Accelerator and Radiation Laboratory, Ankara 06830, Türkiye; Department of Molecular Biology, Genetics and Bioengineering, Graduate School of Engineering and Natural Sciences, Sabanci University, Istanbul 34420, Türkiye; School of Biochemistry, University of Bristol, 1 Tankard's Close, Bristol BS8 1TD, UK.
Christiane SchaffitzelSchool of Biochemistry, University of Bristol, 1 Tankard's Close, Bristol BS8 1TD, UK.
Burak Veli KabasakalTurkish Accelerator and Radiation Laboratory, Ankara 06830, Türkiye; School of Biochemistry, University of Bristol, 1 Tankard's Close, Bristol BS8 1TD, UK. Electronic address: bvkabasakal@tarla-fel.org.

Funding

Biotechnology and Biological Sciences Research Council BB/P000940/1Wellcome Trust 210701/Z/18/Z
6 · The paper itself

Abstract

Membrane proteins are essential for bacterial survival, facilitating vital processes such as energy production, nutrient transport, and cell wall synthesis. YidC is a key player in membrane protein biogenesis, acting as both an insertase and a chaperone to ensure proper protein folding and integration into the lipid bilayer. Its conserved structure and adaptability enable it to mediate co-translational and post-translational protein insertion into the membrane through both Sec-dependent and Sec-independent pathways. In addition to facilitating protein insertion, YidC collaborates with FtsH in protein quality control, preventing the accumulation of misfolded proteins that could impair cellular function. This important relationship between YidC and FtsH is poorly understood, and there is a need for further investigation into their collaboration. Understanding how YidC and FtsH coordinate their roles could provide valuable insights into the links between bacterial membrane protein biogenesis and quality control pathways. Moreover, given its central functions, YidC represents a potential target for antimicrobial development. Small molecules disrupting its function in protein folding and insertion, hold promise. However, achieving bacterial specificity without impacting eukaryotic homologs remains a challenge. Here, we review our current understanding of YidC's structure, molecular function in membrane protein biogenesis and quality control, known interactions and its therapeutic potential.

Indexed as

Escherichia coli ProteinsMembrane ProteinsMembrane Transport ProteinsProtein BiosynthesisATP-Dependent ProteasesCell MembraneEscherichia coliProtein FoldingATP-Dependent ProteasesEscherichia coli ProteinsFtsH protein, E coliMembrane ProteinsMembrane Transport ProteinsYIDC protein, E coliChaperoneInsertaseMembrane protein biosynthesisMembrane protein insertionMembrane protein quality controlYidC

Identifiers

PMID40221051
PMCPMC7618853

What OpenQuestion holds

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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.