SHP family protein tyrosine phosphatases adopt canonical active-site conformations in the apo and phosphate-bound states

Protein Pept Lett. 2013 Sep;20(9):1039-48. doi: 10.2174/09298665113209990041.

Abstract

Protein tyrosine phosphatase (PTP) catalytic domains undergo a series of conformational changes in order to mediate dephosphorylation of their tyrosine phosphorylated substrates. An important conformational change occurs in the Tryptophan-Proline-Aspartic acid (WPD) loop, which contains the conserved catalytic aspartate. Upon substrate binding, the WPD loop transitions from the 'open' to the 'closed' state, thus allowing optimal positioning of the catalytic aspartate for substrate dephosphorylation. The dynamics of WPD loop conformational changes have previously been studied for PTP1B, HePTP, and the bacterial phosphatase YopH, but have not yet been comprehensively studied for the nonreceptor tyrosine phosphatase SHP-1 (PTPN6). To structurally describe the changes in WPD loop conformation in SHP-1, we have determined the 1.4 Å crystal structure of the catalytic domain of SHP-1 in the Apo state and the 1.8 Å crystal structure of the SHP-1 catalytic domain in complex with a phosphate ion. We provide structural analysis for the WPD loop closed state of SHP phosphatases and the conformational changes that occur upon WPD loop closure.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Apoenzymes / chemistry
  • Apoenzymes / metabolism
  • Catalytic Domain
  • Crystallization
  • Humans
  • Hydrogen Bonding
  • Models, Molecular
  • Phosphorylation
  • Protein Binding
  • Protein Conformation
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6 / chemistry*
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6 / metabolism
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism

Substances

  • Apoenzymes
  • Recombinant Proteins
  • PTPN6 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6