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A Proteolytic Transmembrane Signaling Pathway and Resistance to β-Lactams in Staphylococci

Zhang, H. Z., Hackbarth, C. J., Chansky, K. M., Chambers, H. F.·2001·Science

Abstract

β-Lactamase and penicillin-binding protein 2a mediate staphylococcal resistance to β-lactam antibiotics, which are otherwise highly clinically effective. Production of these inducible proteins is regulated by a signal-transducing integral membrane protein and a transcriptional repressor. The signal transducer is a fusion protein with penicillin-binding and zinc metalloprotease domains. The signal for protein expression is transmitted by site-specific proteolytic cleavage of both the transducer, which autoactivates, and the repressor, which is inactivated, unblocking gene transcription. Compounds that disrupt this regulatory pathway could restore the activity of β-lactam antibiotics against drug-resistant strains of staphylococci.

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Metadata

Authors
Zhang, H. Z., Hackbarth, C. J., Chansky, K. M., & Chambers, H. F.
Venue
Science
Published
2001-03-09
Volume
291
Issue
5510
Pages
1962-1965
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2148663866
Cited by
252
References
0
FWCI
10.47
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A Proteolytic Transmembrane Signaling Pathway and Resistance to β-Lactams in Staphylococci. https://app.cochat.ai/papers/10.1126/science.1055144
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Zhang, H. Z., Hackbarth, C. J., Chansky, K. M., & Chambers, H. F. (2001). A Proteolytic Transmembrane Signaling Pathway and Resistance to β-Lactams in Staphylococci. Science. https://doi.org/10.1126/science.1055144

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.