ArticleJournal of bacteriology2026
Genome-wide screen identifies novel factors for surface protein cross-wall trafficking and cell envelope homeostasis in
Article in Journal of bacteriology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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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.
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.
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Who cites it
2 citing papers in PubMed.
- Mislocalization of PBPs inMicrobiology spectrum · 2026Article
- Global Transcriptional Differences inAntibiotics (Basel, Switzerland) · 2026Article
Corrections and comments
- Update of
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4 authors.
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Abstract
Cell-wall-anchored surface proteins are integral components of gram-positive bacterial cell envelopes. The trafficking of many surface proteins carrying a YSIRK/G-S signal peptide is synchronized with cell envelope biogenesis during cell division, whereby YSIRK proteins traffic to the septal membrane and anchor to the septal peptidoglycan (cross-wall). Previous work demonstrated that LtaS-mediated lipoteichoic acid (LTA) synthesis restricts YSIRK proteins' septal trafficking. Here, we did a comprehensive immunofluorescence microscopy screen of the entire IMPORTANCE: Surface proteins of gram-positive bacteria are key virulence factors in the human pathogen
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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.