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Nat Chem Biol. 2019 May;15(5):510-518. doi: 10.1038/s41589-019-0265-y. Epub 2019 Apr 8.

Structure of McsB, a protein kinase for regulated arginine phosphorylation.

Author information

1
Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Vienna, Austria.
2
VIB/UGent, Ghent, Belgium.
3
Boehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
4
Institute of Molecular Biotechnology of the Austrian Academy of Science (IMBA), Vienna BioCenter (VBC), Vienna, Austria.
5
Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Vienna, Austria. tim.clausen@imp.ac.at.
6
Medical University of Vienna, Vienna BioCenter (VBC), Vienna, Austria. tim.clausen@imp.ac.at.

Abstract

Protein phosphorylation regulates key processes in all organisms. In Gram-positive bacteria, protein arginine phosphorylation plays a central role in protein quality control by regulating transcription factors and marking aberrant proteins for degradation. Here, we report structural, biochemical, and in vivo data of the responsible kinase, McsB, the founding member of an arginine-specific class of protein kinases. McsB differs in structure and mechanism from protein kinases that act on serine, threonine, and tyrosine residues and instead has a catalytic domain related to that of phosphagen kinases (PhKs), metabolic enzymes that phosphorylate small guanidino compounds. In McsB, the PhK-like phosphotransferase domain is structurally adapted to target protein substrates and is accompanied by a novel phosphoarginine (pArg)-binding domain that allosterically controls protein kinase activity. The identification of distinct pArg reader domains in this study points to a remarkably complex signaling system, thus challenging simplistic views of bacterial protein phosphorylation.

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PMID:
30962626
PMCID:
PMC6522372
[Available on 2019-11-01]
DOI:
10.1038/s41589-019-0265-y
[Indexed for MEDLINE]

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