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5D28

Complex of GM-CSF/IL-2 inhibition factor with Granulocyte-macrophage colony-stimulating factor

Summary for 5D28
Entry DOI10.2210/pdb5d28/pdb
Related5D22
DescriptorGM-CSF/IL-2 inhibition factor, Granulocyte-macrophage colony-stimulating factor, alpha-D-mannopyranose-(1-3)-beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total)
Functional Keywordssignaling protein, cytokine, host-pathogen interactions, immunology, viral protein
Biological sourceOrf virus (ORFV)
More
Total number of polymer chains4
Total formula weight87805.03
Authors
Felix, J.,Savvides, S.N. (deposition date: 2015-08-05, release date: 2016-11-16, Last modification date: 2024-10-16)
Primary citationFelix, J.,Kandiah, E.,De Munck, S.,Bloch, Y.,van Zundert, G.C.,Pauwels, K.,Dansercoer, A.,Novanska, K.,Read, R.J.,Bonvin, A.M.,Vergauwen, B.,Verstraete, K.,Gutsche, I.,Savvides, S.N.
Structural basis of GM-CSF and IL-2 sequestration by the viral decoy receptor GIF.
Nat Commun, 7:13228-13228, 2016
Cited by
PubMed Abstract: Subversion of the host immune system by viruses is often mediated by molecular decoys that sequester host proteins pivotal to mounting effective immune responses. The widespread mammalian pathogen parapox Orf virus deploys GIF, a member of the poxvirus immune evasion superfamily, to antagonize GM-CSF (granulocyte macrophage colony-stimulating factor) and IL-2 (interleukin-2), two pleiotropic cytokines of the mammalian immune system. However, structural and mechanistic insights into the unprecedented functional duality of GIF have remained elusive. Here we reveal that GIF employs a dimeric binding platform that sequesters two copies of its target cytokines with high affinity and slow dissociation kinetics to yield distinct complexes featuring mutually exclusive interaction footprints. We illustrate how GIF serves as a competitive decoy receptor by leveraging binding hotspots underlying the cognate receptor interactions of GM-CSF and IL-2, without sharing any structural similarity with the cytokine receptors. Our findings contribute to the tracing of novel molecular mimicry mechanisms employed by pathogenic viruses.
PubMed: 27819269
DOI: 10.1038/ncomms13228
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.845 Å)
Structure validation

227344

數據於2024-11-13公開中

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