Publications by authors named "Csaba Adam"

We have developed a unified, versatile vector set for expression of recombinant proteins, fit for use in any bacterial, yeast, insect or mammalian cell host. The advantage of this system is its versatility at the vector level, achieved by the introduction of a novel expression cassette. This cassette contains a unified multi-cloning site, affinity tags, protease cleavable linkers, an optional secretion signal, and common restriction endonuclease sites at key positions.

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Background: Cells deploy quality control mechanisms to remove damaged or misfolded proteins. Recently, we have reported that a mutation (R43W) in the Frank-ter Haar syndrome protein Tks4 resulted in aberrant intracellular localization.

Results: Here we demonstrate that the accumulation of Tks4(R43W) depends on the intact microtubule network.

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The genome of the filamentous fungus Aspergillus nidulans harbors the gene ppzA that codes for the catalytic subunit of protein phosphatase Z (PPZ), and the closely related opportunistic pathogen Aspergillus fumigatus encompasses a highly similar PPZ gene (phzA). When PpzA and PhzA were expressed in Saccharomyces cerevisiae or Schizosaccharomyces pombe they partially complemented the deleted phosphatases in the ppz1 or the pzh1 mutants, and they also mimicked the effect of Ppz1 overexpression in slt2 MAP kinase deficient S. cerevisiae cells.

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The opportunistic pathogen Candida albicans has a single protein phosphatase Z (PPZ) candidate gene termed CaPPZ1, which shows significant allele variability. We demonstrate here that bacterially expressed CaPpz1 protein exhibits phosphatase activity which can be inhibited by recombinant Hal3, a known inhibitor of Saccharomyces cerevisiae Ppz1. Site-directed mutagenesis experiments based on natural polymorphisms allowed the identification of three amino acid residues that affect enzyme activity or stability.

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Article Synopsis
  • Phosphoprotein phosphatases (PPP) are crucial regulatory enzymes found in all eukaryotes, and research on 12 Drosophila species shows a significant expansion of their gene family from a core set of 8 essential phosphatases.
  • Retropositions and tandem gene duplications added to the diversity of PPP genes, while occasional gene losses led to species-specific variations; notably, five uncharacterized phosphatase retrogenes were identified, showing male-specific expression in certain Drosophila.
  • Evolutionary changes also impacted the intron-exon structure and chromosomal location of PPP genes, with a decline in G-C content linked to movement into the heterochromatic region of chromosome Y, highlighting the dynamic nature of
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In the genome of Drosophila melanogaster, there are 19 phosphoprotein phosphatase (PPP) catalytic subunit coding genes. Seven of the novel members of the gene family turned out to be Drosophila-specific. The expression and evolution of these genes was investigated in the present study.

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