Cutting edge: molecular structure of the IL-1R-associated kinase-4 death domain and its implications for TLR signaling

J Immunol. 2005 Oct 1;175(7):4175-9. doi: 10.4049/jimmunol.175.7.4175.

Abstract

IL-1R-associated kinase (IRAK) 4 is an essential component of innate immunity. IRAK-4 deficiency in mice and humans results in severe impairment of IL-1 and TLR signaling. We have solved the crystal structure for the death domain of Mus musculus IRAK-4 to 1.7 A resolution. This is the first glimpse of the structural details of a mammalian IRAK family member. The crystal structure reveals a six-helical bundle with a prominent loop, which among IRAKs and Pelle, a Drosophila homologue, is unique to IRAK-4. This highly structured loop contained between helices two and three, comprises an 11-aa stretch. Although innate immune domain recognition is thought to be very similar between Drosophila and mammals, this structural component points to a drastic difference. This structure can be used as a framework for future mutation and deletion studies and potential drug design.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Crystallography, X-Ray
  • Drosophila Proteins / chemistry
  • Interleukin-1 Receptor-Associated Kinases
  • Mice
  • Molecular Sequence Data
  • Phosphotransferases (Alcohol Group Acceptor) / chemistry*
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Protein Serine-Threonine Kinases / chemistry
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Signal Transduction / physiology*
  • Structural Homology, Protein

Substances

  • Drosophila Proteins
  • Phosphotransferases (Alcohol Group Acceptor)
  • pll protein, Drosophila
  • Interleukin-1 Receptor-Associated Kinases
  • Irak4 protein, mouse
  • Protein Serine-Threonine Kinases

Associated data

  • PDB/2A9I