8GJW
Structure of a cGAS-like receptor Cv-cGLR1 from C. virginica
Summary for 8GJW
Entry DOI | 10.2210/pdb8gjw/pdb |
Descriptor | cGAS-like receptor 1, SULFATE ION (3 entities in total) |
Functional Keywords | pattern recognition receptor, cgas, innate immunity, cgas-like receptor, immune system |
Biological source | Crassostrea virginica (eastern oyster) |
Total number of polymer chains | 1 |
Total formula weight | 41788.27 |
Authors | Li, Y.,Morehouse, B.R.,Slavik, K.M.,Liu, J.,Toyoda, H.,Kranzusch, P.J. (deposition date: 2023-03-16, release date: 2023-07-05, Last modification date: 2024-05-22) |
Primary citation | Li, Y.,Slavik, K.M.,Toyoda, H.C.,Morehouse, B.R.,de Oliveira Mann, C.C.,Elek, A.,Levy, S.,Wang, Z.,Mears, K.S.,Liu, J.,Kashin, D.,Guo, X.,Mass, T.,Sebe-Pedros, A.,Schwede, F.,Kranzusch, P.J. cGLRs are a diverse family of pattern recognition receptors in innate immunity. Cell, 186:3261-3276.e20, 2023 Cited by PubMed Abstract: Cyclic GMP-AMP synthase (cGAS) is an enzyme in human cells that controls an immune response to cytosolic DNA. Upon binding DNA, cGAS synthesizes a nucleotide signal 2'3'-cGAMP that activates STING-dependent downstream immunity. Here, we discover that cGAS-like receptors (cGLRs) constitute a major family of pattern recognition receptors in innate immunity. Building on recent analysis in Drosophila, we identify >3,000 cGLRs present in nearly all metazoan phyla. A forward biochemical screening of 150 animal cGLRs reveals a conserved mechanism of signaling including response to dsDNA and dsRNA ligands and synthesis of isomers of the nucleotide signals cGAMP, c-UMP-AMP, and c-di-AMP. Combining structural biology and in vivo analysis in coral and oyster animals, we explain how synthesis of distinct nucleotide signals enables cells to control discrete cGLR-STING signaling pathways. Our results reveal cGLRs as a widespread family of pattern recognition receptors and establish molecular rules that govern nucleotide signaling in animal immunity. PubMed: 37379839DOI: 10.1016/j.cell.2023.05.038 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.93 Å) |
Structure validation
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