8JYX
Crystal structure of the gasdermin-like protein RCD-1-1 from Neurospora crassa
Summary for 8JYX
Entry DOI | 10.2210/pdb8jyx/pdb |
Related PRD ID | PRD_900001 |
Descriptor | Maltodextrin-binding protein,Gasdermin-like protein rcd-1-1, alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose (3 entities in total) |
Functional Keywords | pyroptosis, gasdermnin, allorecognition, immune system |
Biological source | Escherichia coli More |
Total number of polymer chains | 2 |
Total formula weight | 139915.31 |
Authors | |
Primary citation | Li, 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: 38662913DOI: 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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