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8GJZ

Structure of a STING receptor from S. pistillata Sp-STING1 bound to 2'3'-cUA

Summary for 8GJZ
Entry DOI10.2210/pdb8gjz/pdb
Related8EFM
DescriptorStimulator of interferon genes protein, 2'3'-cUA (3 entities in total)
Functional Keywordssting, cyclic dinucleotide, innate immunity, cgas, immune system
Biological sourceStylophora pistillata
Total number of polymer chains2
Total formula weight44345.29
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 citationLi, 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: 37379839
DOI: 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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