Characterization of the threonine-phosphatase of mouse eyes absent 3

FEBS Lett. 2011 Sep 2;585(17):2714-9. doi: 10.1016/j.febslet.2011.07.029. Epub 2011 Aug 2.

Abstract

Eyes absent (EYA) has tyrosine- and threonine-phosphatase activities in their C-terminal and N-terminal regions, respectively. Using various mutants of mouse EYA3, we showed that the 68-amino acid domain between positions 53 and 120 was necessary and sufficient for its threonine-phosphatase activity. Point mutations were then introduced, and residues Cys-56, Tyr-77, His-79, and Tyr-90 were essential for the EYA3s threonine-phosphatase. The 68-amino acid domain is not well conserved among the four mouse EYA members, but is evolutionally highly conserved in the orthologous EYA members of different species, suggesting that the threonine-phosphatase of EYA3 has a function distinct from that of the other EYAs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Mice
  • Mutagenesis, Site-Directed
  • Phosphoprotein Phosphatases / chemistry
  • Phosphoprotein Phosphatases / genetics
  • Phosphoprotein Phosphatases / metabolism*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Structure-Activity Relationship
  • Trans-Activators / chemistry
  • Trans-Activators / genetics
  • Trans-Activators / metabolism

Substances

  • DNA-Binding Proteins
  • Eya3 protein, mouse
  • Eya4 protein, mouse
  • Recombinant Proteins
  • Trans-Activators
  • Phosphoprotein Phosphatases