8GJZ
Structure of a STING receptor from S. pistillata Sp-STING1 bound to 2'3'-cUA
Summary for 8GJZ
| Entry DOI | 10.2210/pdb8gjz/pdb |
| Related | 8EFM |
| Descriptor | Stimulator of interferon genes protein, 2'3'-cUA (3 entities in total) |
| Functional Keywords | sting, cyclic dinucleotide, innate immunity, cgas, immune system |
| Biological source | Stylophora pistillata |
| Total number of polymer chains | 2 |
| Total formula weight | 44345.29 |
| Authors | Li, Y.,Toyoda, H.,Slavik, K.M.,Morehouse, B.R.,Kranzusch, P.J. (deposition date: 2023-03-16, release date: 2023-07-05, Last modification date: 2024-11-13) |
| 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 (2.92 Å) |
Structure validation
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