Structural anomalies in a published NMR-derived structure of IRAK-M

Hessel Poelman, Hans Ippel, Berke Gürkan, Rolf Boelens, Gert Vriend, Cornelis van ‘t Veer, Esther Lutgens, Gerry A.F. Nicolaes

Research output: Contribution to journalArticlepeer-review


Signaling by Toll-Like Receptors and the Interleukin-1 Receptor (IL1-R) involves intracellular binding of MyD88, followed by assembly of IL1-R Associated Kinases (IRAKs) into the so-called Myddosome. Using NMR, Nechama et al. determined the structure of the IRAK-M death domain monomer (PDBid: 5UKE). With this structure, they performed a docking study to model the location of IRAK-M in the Myddosome. Based on this, they present a molecular basis for selectivity of IRAK-M towards IRAK1 over IRAK2 binding. When we attempted to use 5UKE as a homology modeling template, we noticed that our 5UKE-based models had structural issues, such as disallowed torsion angles and solvent exposed tryptophans. We therefore analyzed the NMR ensemble of 5UKE using structure validation tools and we compared 5UKE with homologous high-resolution X-ray structures. We identified several structural anomalies in 5UKE, including packing issues, frayed helices and improbable side chain conformations. We used Yasara to build a homology model, based on two high resolution death domain crystal structures, as an alternative model for the IRAK-M death domain (atomic coordinates, modeling details and validation are available at Our model agrees better with known death domain structure information than 5UKE and also with the chemical shift data that was deposited for 5UKE.

Original languageEnglish (US)
Article number108061
JournalJournal of Molecular Graphics and Modelling
StatePublished - Mar 2022


  • 5UKE
  • DALI
  • Homology modeling
  • IRAK-M
  • Myddosome
  • NMR
  • Structure validation
  • Yasara

ASJC Scopus subject areas

  • Spectroscopy
  • Physical and Theoretical Chemistry
  • Computer Graphics and Computer-Aided Design
  • Materials Chemistry


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