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9MW9

Cryo-EM structure of CRISPR-associated cA4 bound Cat1 Trigonal filament assembly

Summary for 9MW9
Entry DOI10.2210/pdb9mw9/pdb
EMDB information48698
DescriptorRNA (5'-R(P*AP*AP*AP*A)-3'), Cat1 (CRISPR-associated TIR 1) (2 entities in total)
Functional Keywordscrispr, antiphage defense, adaptive immunity, filament, carf, tir, ca4, antiviral protein
Biological sourcebacterium
More
Total number of polymer chains33
Total formula weight677303.55
Authors
Majumder, P.,Patel, D.J. (deposition date: 2025-01-17, release date: 2025-04-16, Last modification date: 2025-04-23)
Primary citationBaca, C.F.,Majumder, P.,Hickling, J.H.,Patel, D.J.,Marraffini, L.A.
Cat1 forms filament networks to degrade NAD + during the type III CRISPR-Cas antiviral response.
Science, :eadv9045-eadv9045, 2025
Cited by
PubMed Abstract: Type III CRISPR-Cas systems defend against viral infection in prokaryotes using an RNA-guided complex that recognizes foreign transcripts and synthesizes cyclic oligo-adenylate (cOA) messengers to activate CARF immune effectors. Here we investigated a protein containing a CARF domain fused Toll/interleukin-1 receptor (TIR) domain, Cat1. We found that Cat1 provides immunity by cleaving and depleting NAD molecules from the infected host, inducing a growth arrest that prevents viral propagation. Cat1 forms dimers that stack upon each other to generate long filaments that are maintained by bound cOA ligands, with stacked TIR domains forming the NAD cleavage catalytic sites. Further, Cat1 filaments assemble into unique trigonal and pentagonal networks that enhance NAD degradation. Cat1 presents an unprecedented chemistry and higher-order protein assembly for the CRISPR-Cas response.
PubMed: 40208959
DOI: 10.1126/science.adv9045
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3 Å)
Structure validation

237735

数据于2025-06-18公开中

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