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Identification of Multiple Substrates of the StkP Ser/Thr Protein Kinase in Streptococcus pneumoniae
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SYSNO ASEP 0348138 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Identification of Multiple Substrates of the StkP Ser/Thr Protein Kinase in Streptococcus pneumoniae Author(s) Nováková, Linda (MBU-M) RID
Bezoušková, Silvia (MBU-M)
Pompach, Petr (MBU-M) RID, ORCID
Přenosilová, Lenka (MBU-M)
Weiser, Jaroslav (MBU-M) RID
Branny, Pavel (MBU-M) RID, ORCIDSource Title Journal of Bacteriology. - : American Society for Microbiology - ISSN 0021-9193
Roč. 192, č. 14 (2010), s. 3629-3638Number of pages 10 s. Language eng - English Country US - United States Keywords GROUP-B STREPTOCOCCUS ; EUKARYOTIC-TYPE ; SERINE/THREONINE KINASE Subject RIV EE - Microbiology, Virology R&D Projects GA204/08/0783 GA ČR - Czech Science Foundation (CSF) IAA600200801 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR) GP204/07/P082 GA ČR - Czech Science Foundation (CSF) CEZ AV0Z50200510 - MBU-M (2005-2011) UT WOS 000279183300008 DOI 10.1128/JB.01564-09 Annotation The human pathogen Streptococcus pneumoniae encodes a single copy of a eukaryotic-like Ser/Thr protein kinase gene designated stkP. Previous studies demonstrated the pleiotropic role of the transmembrane protein kinase StkP in pneumococcal physiology. StkP regulates virulence, competence, and stress resistance and plays a role in the regulation of gene expression. In this study we identified three new substrates of StkP: the Mn-dependent inorganic pyrophosphatase PpaC, the hypothetical protein spr0334, and the cell division protein DivIVA. We showed that StkP activation and substrate recognition depend on the presence of a peptidoglycan-binding domain comprising four PASTA domain repeats. We found that StkP is regulated in a growth-dependent manner and likely senses intracellular peptidoglycan subunits present in the cell division septa Workplace Institute of Microbiology Contact Eliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231 Year of Publishing 2011
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