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Structure of a pseudokinase-domain switch that controls oncogenic activation of Jak kinases

  • Angela V. Toms
  • , Anagha Deshpande
  • , Randall McNally
  • , Youngjee Jeong
  • , Julia M. Rogers
  • , Chae Un Kim
  • , Sol M. Gruner
  • , Scott B. Ficarro
  • , Jarrod A. Marto
  • , Martin Sattler
  • , James D. Griffin
  • , Michael J. Eck
  • Harvard University
  • Dana-Farber Cancer Institute
  • Cornell University

Research output: Contribution to journalArticlepeer-review

92 Scopus citations

Abstract

The V617F mutation in the Jak2 pseudokinase domain causes myeloproliferative neoplasms, and the equivalent mutation in Jak1 (V658F) is found in T-cell leukemias. Crystal structures of wild-type and V658F-mutant human Jak1 pseudokinase reveal a conformational switch that remodels a linker segment encoded by exon 12, which is also a site of mutations in Jak2. This switch is required for V617F-mediated Jak2 activation and possibly for physiologic Jak activation.

Original languageEnglish
Pages (from-to)1221-1224
Number of pages4
JournalNature Structural and Molecular Biology
Volume20
Issue number10
DOIs
StatePublished - Oct 2013

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