Reciprocal allosteric regulation of p38γ and PTPN3 involves a PDZ domain-modulated complex formation

Kai En Chen, Shu Yu Lin, Mei Ju Wu, Meng Ru Ho, Abirami Santhanam, Chia Cheng Chou, Tzu Ching Meng, Andrew H.J. Wang

Research output: Contribution to journalArticlepeer-review

13 Citations (Scopus)

Abstract

The mitogen-activated protein kinase p38γ (also known as MAPK12) and its specific phosphatase PTPN3 (also known as PTPH1) cooperate to promote Ras-induced oncogenesis. We determined the architecture of the PTPN3-p38γ complex by a hybrid method combining X-ray crystallography, small-angle X-ray scattering, and chemical cross-linking coupled to mass spectrometry. A unique feature of the glutamic acid-containing loop (E-loop) of the phosphatase domain defined the substrate specificity of PTPN3 toward fully activated p38γ. The solution structure revealed the formation of an active-state complex between p38γ and the phosphatase domain of PTPN3. The PDZ domain of PTPN3 stabilized the active-state complex through an interaction with the PDZ-binding motif of p38γ. This interaction alleviated autoinhibition of PTPN3, enabling efficient tyrosine dephosphorylation of p38γ. Our findings may enable structure-based drug design targeting the PTPN3-p38γ interaction as an anticancer therapeutic.

Original languageEnglish
Pages (from-to)ra98
JournalScience Signaling
Volume7
Issue number347
DOIs
Publication statusPublished - Oct 14 2014

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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