5vmo

Crystal structure of grouper iridovirus GIV66:Bim complex

spinqualitylabelsall models 5vmo, resolution 1.70Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 5vmo is a 2 chain structure with sequence from Danio rerio and Grouper iridovirus. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 1.7Å Ligands: 1PE, EDO Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function Q5GAF0_9VIRU Publication Abstract from PubMed Programmed cell death or apoptosis is a critical mechanism for the controlled removal of damaged or infected cells, and proteins of the BCL-2 family are important arbiters of this process. Viruses have been shown to encode functional and structural homologs of BCL-2 to counter premature host-cell apoptosis and ensure viral proliferation or survival. Grouper iridovirus (GIV) is a large DNA virus belonging to the Iridoviridae family and harbors GIV66, a putative BCL-2 like protein and mitochondrially localized apoptosis inhibitor. However, the molecular and structural bases of GIV66-mediated apoptosis inhibition is currently not understood. To gain insight into GIV66's mechanism of action, we systematically evaluated its ability to bind peptides spanning the BH3 domain of pro-apoptotic BCL-2 family members. Our results revealed that GIV66 harbors an unusually high level of specificity for pro-apoptotic BCL-2 and displays affinity only for BCL2-like 11 (BCL2L11 or BIM). Using crystal structures of both apo GIV66 and GIV66 bound to the BH3 domain from BIM, we unexpectedly found that GIV66 forms dimers via an interface that results in occluded access to the canonical BCL-2 ligand-binding groove, which breaks apart upon BIM binding. This observation suggests that GIV66 dimerization may affect GIV66's ability to bind host pro-death BCL-2 proteins, and enables highly targeted virus directed suppression of host apoptosis signalling. Our findings provide a mechanistic understanding for the potent antiapoptotic activity of GIV66 by identifying it as the first single-specificity, pro-survival BCL-2 protein, and identifying a pivotal role of BIM in GIV-mediated inhibition of apoptosis. Grouper Iridovirus GIV66 is a Bcl-2 protein that inhibits apoptosis by exclusively sequestering Bim.,Banjara S, Mao J, Ryan TM, Caria S, Kvansakul M J Biol Chem. 2018 Feb 26. pii: RA117.000591. doi: 10.1074/jbc.RA117.000591. PMID:29483196 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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