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8JYX

Crystal structure of the gasdermin-like protein RCD-1-1 from Neurospora crassa

Summary for 8JYX
Entry DOI10.2210/pdb8jyx/pdb
Related PRD IDPRD_900001
DescriptorMaltodextrin-binding protein,Gasdermin-like protein rcd-1-1, alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose (3 entities in total)
Functional Keywordspyroptosis, gasdermnin, allorecognition, immune system
Biological sourceEscherichia coli
More
Total number of polymer chains2
Total formula weight139915.31
Authors
Li, Y.,Hou, Y.J.,Ding, J. (deposition date: 2023-07-04, release date: 2024-05-08, Last modification date: 2024-05-29)
Primary citationLi, Y.,Hou, Y.,Sun, Q.,Zeng, H.,Meng, F.,Tian, X.,He, Q.,Shao, F.,Ding, J.
Cleavage-independent activation of ancient eukaryotic gasdermins and structural mechanisms.
Science, 384:adm9190-adm9190, 2024
Cited by
PubMed Abstract: Gasdermins (GSDMs) are pore-forming proteins that execute pyroptosis for immune defense. GSDMs are two-domain proteins activated by proteolytic removal of the inhibitory domain. In this work, we report two types of cleavage-independent GSDM activation. First, GSDM, a pore-forming domain-only protein from the basal metazoan , is a disulfides-linked autoinhibited dimer activated by reduction of the disulfides. The cryo-electron microscopy (cryo-EM) structure illustrates the assembly mechanism for the 44-mer GSDM pore. Second, RCD-1-1 and RCD-1-2, encoded by the polymorphic () gene in filamentous fungus , are also pore-forming domain-only GSDMs. RCD-1-1 and RCD-1-2, when encountering each other, form pores and cause pyroptosis, underlying allorecognition in . The cryo-EM structure reveals a pore of 11 RCD-1-1/RCD-1-2 heterodimers and a heterodimerization-triggered pore assembly mechanism. This study shows mechanistic diversities in GSDM activation and indicates versatile functions of GSDMs.
PubMed: 38662913
DOI: 10.1126/science.adm9190
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.35 Å)
Structure validation

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PDB entries from 2024-11-20

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