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Structure of a Novel Winged-Helix Like Domain from Human NFRKB Protein

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% disorde...

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Detalles Bibliográficos
Autores principales: Kumar, Abhinav, Möcklinghoff, Sabine, Yumoto, Fumiaki, Jaroszewski, Lukasz, Farr, Carol L., Grzechnik, Anna, Nguyen, Phuong, Weichenberger, Christian X., Chiu, Hsiu-Ju, Klock, Heath E., Elsliger, Marc-André, Deacon, Ashley M., Godzik, Adam, Lesley, Scott A., Conklin, Bruce R., Fletterick, Robert J., Wilson, Ian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439487/
https://www.ncbi.nlm.nih.gov/pubmed/22984442
http://dx.doi.org/10.1371/journal.pone.0043761
Descripción
Sumario: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.