PLoS ONE (Jan 2012)

Structure of a novel winged-helix like domain from human NFRKB protein.

  • Abhinav Kumar,
  • Sabine Möcklinghoff,
  • Fumiaki Yumoto,
  • Lukasz Jaroszewski,
  • Carol L Farr,
  • Anna Grzechnik,
  • Phuong Nguyen,
  • Christian X Weichenberger,
  • Hsiu-Ju Chiu,
  • Heath E Klock,
  • Marc-André Elsliger,
  • Ashley M Deacon,
  • Adam Godzik,
  • Scott A Lesley,
  • Bruce R Conklin,
  • Robert J Fletterick,
  • Ian A Wilson

DOI
https://doi.org/10.1371/journal.pone.0043761
Journal volume & issue
Vol. 7, no. 9
p. e43761

Abstract

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The human nuclear factor related to kappa-B-binding protein (NFRKB) is a 1299-residue protein that is a component of the metazoan INO80 complex involved in chromatin remodeling, transcription regulation, DNA replication and DNA repair. Although full length NFRKB is predicted to be around 65% disordered, comparative sequence analysis identified several potentially structured sections in the N-terminal region of the protein. These regions were targeted for crystallographic studies, and the structure of one of these regions spanning residues 370-495 was determined using the JCSG high-throughput structure determination pipeline. The structure reveals a novel, mostly helical domain reminiscent of the winged-helix fold typically involved in DNA binding. However, further analysis shows that this domain does not bind DNA, suggesting it may belong to a small group of winged-helix domains involved in protein-protein interactions.