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9UVF

Crystal structure of Sec23a/24a/22b bound to mouse STING LI motif

Summary for 9UVF
Entry DOI10.2210/pdb9uvf/pdb
DescriptorProtein transport protein Sec23A, Protein transport protein Sec24A, Vesicle-trafficking protein SEC22b, ... (5 entities in total)
Functional Keywordssting, copii, cgas, protein trafficking, innate immunity, transport protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains4
Total formula weight189452.61
Authors
Ma, W.F. (deposition date: 2025-05-10, release date: 2026-05-06)
Primary citationNan, Y.,Cui, D.,Guo, J.,Ma, X.,Wang, J.,Guo, L.,Li, T.,Yang, M.,Huang, G.,Xu, A.,Ma, W.
STING COPII ER Export Trafficking and Signaling Primed by Phosphorylation Switches.
Adv Sci, 12:e03660-e03660, 2025
Cited by
PubMed Abstract: Despite advances in understanding the STING signaling pathway, mechanisms governing cyclic GMP-AMP (cGAMP)-induced STING trafficking out of the endoplasmic reticulum (ER) remain unclear. This study reveals that STING localization is regulated by the balance between coat protein II (COPII)- and coat protein I (COPI)-mediated trafficking, maintaining ER residency in the inactive state or promoting transport to the cis-Golgi via enhanced COPII-mediated export upon activation. Two novel TANK-binding kinase 1 (TBK1)-regulated phosphorylated COPII sorting signals on STING-a conserved pSGME motif and a primate-specific pFS motif-are biochemically and structurally identified. These cGAMP-induced signals drive activated STING toward the ER-Golgi intermediate compartment (ERGIC) and the cis-Golgi complex. Using a cell-free COPII vesicle reconstitution system, TBK1 activation is shown to occur on COPII vesicles, while IRF3 phosphorylation is confined to the ERGIC or the cis-Golgi complex post-uncoating, due to the competitive binding of COPII Sec24 and IRF3 to phosphorylated STING. A class of compounds is also identified that attenuates IRF3 phosphorylation by inhibiting phosphorylated STING packaging into COPII vesicles. These findings elucidate STING trafficking mechanisms and offer therapeutic potential for diseases linked to dysregulated STING activation.
PubMed: 40598830
DOI: 10.1002/advs.202503660
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.15 Å)
Structure validation

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