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Recognition of peptidoglycan and beta-lactam antibiotics by the extracellular domain of the Ser/Thr protein kinase StkP from Streptococcus pneumoniae

  1. 1.
    SYSNO ASEP0370932
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleRecognition of peptidoglycan and beta-lactam antibiotics by the extracellular domain of the Ser/Thr protein kinase StkP from Streptococcus pneumoniae
    Author(s) Maestro, B. (ES)
    Nováková, Linda (MBU-M) RID
    Hesek, D. (US)
    Lee, M. (US)
    Leyva, E. (ES)
    Mobashery, S. (US)
    Sanz, J.M. (ES)
    Branny, Pavel (MBU-M) RID, ORCID
    Source TitleFEBS Letters. - : Wiley - ISSN 0014-5793
    Roč. 585, č. 2 (2011), s. 357-363
    Number of pages7 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsSignal transduction ; Penicillin-binding protein and Ser/Thr protein kinase-associated domain ; Peptidoglycan
    Subject RIVCE - Biochemistry
    R&D ProjectsGP204/07/P082 GA ČR - Czech Science Foundation (CSF)
    GA204/08/0783 GA ČR - Czech Science Foundation (CSF)
    IAA600200801 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z50200510 - MBU-M (2005-2011)
    UT WOS000286180300016
    DOI10.1016/j.febslet.2010.12.016
    AnnotationThe eukaryotic-type serine/threonine kinase StkP from Streptococcus pneumoniae is an important signal-transduction element that regulates the expression of numerous pneumococcal genes. We have expressed the extracellular C-terminal domain of StkP kinase (C-StkP), elaborated a three-dimensional structural model and performed a spectroscopical characterization of its structure and stability. Biophysical experiments show that C-StkP binds to synthetic samples of the cell wall peptidoglycan (PGN) and to beta-lactam antibiotics, which mimic the terminal portions of the PGN stem peptide. This is the first experimental report on the recognition of a minimal PGN unit by a PASTA-containing kinase, suggesting that non-crosslinked PGN may act as a signal for StkP function and pointing to this protein as an interesting target for beta-lactam antibiotics.
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2012
Number of the records: 1  

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