Title of article :
CG15031/PPYR1 is an intrinsically unstructured protein that interacts with protein phosphatase Y
Author/Authors :
K?kai، نويسنده , , Endre and Tantos، نويسنده , , ?gnes and Vissi، نويسنده , , Emese and Sz??r، نويسنده , , Bal?zs and Tompa، نويسنده , , Péter and Gausz، نويسنده , , J?nos and Alphey، نويسنده , , Luke and Friedrich، نويسنده , , Péter and Dombr?di، نويسنده , , Viktor، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Abstract :
Protein phosphatase Y (PPY) is a Drosophila testis-specific enzyme of unknown function. In a yeast two-hybrid screen we identified CG15031/PPYR1 as a PPY interacting protein. The specificity of the protein–protein interaction was proven by directed two-hybrid tests. The complex formation between PPY and PPYR1 was confirmed under in vitro and in vivo conditions by plasmon resonance spectroscopy, co-immunoprecipitation, and pull down experiments. Recombinant PPYR1 expressed in Escherichia coli is a heatstable, protease sensitive, intrinsically unstructured RNA-binding protein that migrates anomalously in SDS–polyacrylamide gel electrophoresis. It can be phosphorylated by cAMP-dependent protein kinase in vitro. PPYR1 moderately inhibits PPY activity, the inhibitory potential of the protein is slightly increased by phosphorylation. We suggest that PPYR1 may function as a scaffolding protein that targets PPY to RNA and other protein partners in Drosophila melanogaster.
Keywords :
intrinsically unstructured protein , protein phosphorylation , Protein phosphatases Y , Protein–protein interaction , CG15031 gene product , Heat-stable unstructured RNA-binding protein , Drosophila melanogaster
Journal title :
Archives of Biochemistry and Biophysics
Journal title :
Archives of Biochemistry and Biophysics