- EMDB-29493: Cryo-EM structure of human Needle/NAIP/NLRC4 (R288A) -
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Basic information
Entry
Database: EMDB / ID: EMD-29493
Title
Cryo-EM structure of human Needle/NAIP/NLRC4 (R288A)
Map data
Sample
Complex: the complex of Needle, human NAIP and NLRC4
Complex: human NAIP and NLRC4
Protein or peptide: Baculoviral IAP repeat-containing protein 1
Protein or peptide: NLR family CARD domain-containing protein 4
Complex: Burkholderia Needle (chimeric with an anthrax toxin lethal factor tag)
Protein or peptide: Lethal factor,Type III secretion system protein
Ligand: ADENOSINE-5'-TRIPHOSPHATE
Ligand: ZINC ION
Keywords
NLRC4 / NAIP / Inflammasome / IMMUNE SYSTEM
Function / homology
Function and homology information
anthrax lethal factor endopeptidase / IPAF inflammasome complex / The IPAF inflammasome / icosanoid biosynthetic process / canonical inflammasome complex / caspase binding / type III protein secretion system complex / positive regulation of protein processing / protein secretion by the type III secretion system / cysteine-type endopeptidase inhibitor activity involved in apoptotic process ...anthrax lethal factor endopeptidase / IPAF inflammasome complex / The IPAF inflammasome / icosanoid biosynthetic process / canonical inflammasome complex / caspase binding / type III protein secretion system complex / positive regulation of protein processing / protein secretion by the type III secretion system / cysteine-type endopeptidase inhibitor activity involved in apoptotic process / pattern recognition receptor signaling pathway / host cell cytosol / TP53 Regulates Transcription of Caspase Activators and Caspases / pyroptotic inflammatory response / Uptake and function of anthrax toxins / cysteine-type endopeptidase inhibitor activity / negative regulation of tumor necrosis factor-mediated signaling pathway / endopeptidase activator activity / detection of bacterium / protein serine/threonine kinase binding / activation of innate immune response / positive regulation of interleukin-1 beta production / positive regulation of JNK cascade / protein homooligomerization / metalloendopeptidase activity / positive regulation of inflammatory response / metallopeptidase activity / positive regulation of NF-kappaB transcription factor activity / nervous system development / toxin activity / basolateral plasma membrane / regulation of apoptotic process / negative regulation of neuron apoptotic process / defense response to bacterium / positive regulation of apoptotic process / inflammatory response / innate immune response / intracellular membrane-bounded organelle / apoptotic process / negative regulation of apoptotic process / cell surface / magnesium ion binding / protein homodimerization activity / ATP hydrolysis activity / proteolysis / extracellular region / zinc ion binding / ATP binding / metal ion binding / identical protein binding / plasma membrane / cytosol / cytoplasm Similarity search - Function
Baculoviral IAP repeat-containing protein 1 / NLR family CARD domain-containing protein 4 / NLRC4, helical domain / : / NLRC4 helical domain / Nlrc4-like, winged helix domain / Anthrax toxin lethal factor, central domain / Anthrax toxin lethal factor, middle domain / Type III secretion, needle-protein-like / Type III secretion, needle-protein-like superfamily ...Baculoviral IAP repeat-containing protein 1 / NLR family CARD domain-containing protein 4 / NLRC4, helical domain / : / NLRC4 helical domain / Nlrc4-like, winged helix domain / Anthrax toxin lethal factor, central domain / Anthrax toxin lethal factor, middle domain / Type III secretion, needle-protein-like / Type III secretion, needle-protein-like superfamily / Type III secretion needle MxiH, YscF, SsaG, EprI, PscF, EscF / Type III secretion system, needle protein / Anthrax toxin, lethal/endema factor / Anthrax toxin, lethal/endema factor, N-/C-terminal / : / Anthrax toxin lethal factor, N- and C-terminal domain / Anthrax toxin lethal factor (ATLF)-like domain profile. / BIR repeat. / NACHT nucleoside triphosphatase / NACHT domain / NACHT-NTPase domain profile. / BIR repeat / Inhibitor of Apoptosis domain / BIR repeat profile. / Baculoviral inhibition of apoptosis protein repeat / CARD domain / CARD caspase recruitment domain profile. / Caspase recruitment domain / Metallopeptidase, catalytic domain superfamily / Death-like domain superfamily / Leucine-rich repeat domain superfamily / Neutral zinc metallopeptidases, zinc-binding region signature. / ATPases associated with a variety of cellular activities / AAA+ ATPase domain / P-loop containing nucleoside triphosphate hydrolase Similarity search - Domain/homology
Lethal factor / Baculoviral IAP repeat-containing protein 1 / Type III secretion system protein / NLR family CARD domain-containing protein 4 Similarity search - Component
Journal: Nat Struct Mol Biol / Year: 2024 Title: Structural basis of the human NAIP/NLRC4 inflammasome assembly and pathogen sensing. Authors: Rosalie E Matico / Xiaodi Yu / Robyn Miller / Sandeep Somani / M Daniel Ricketts / Nikit Kumar / Ruth A Steele / Quintus Medley / Scott Berger / Benjamin Faustin / Sujata Sharma / Abstract: The NLR family caspase activation and recruitment domain-containing 4 (NLRC4) inflammasome is a critical cytosolic innate immune machine formed upon the direct sensing of bacterial infection and in ...The NLR family caspase activation and recruitment domain-containing 4 (NLRC4) inflammasome is a critical cytosolic innate immune machine formed upon the direct sensing of bacterial infection and in response to cell stress during sterile chronic inflammation. Despite its major role in instigating the subsequent host immune response, a more complete understanding of the molecular events in the formation of the NLRC4 inflammasome in humans is lacking. Here we identify Bacillus thailandensis type III secretion system needle protein (Needle) as a potent trigger of the human NLR family apoptosis inhibitory protein (NAIP)/NLRC4 inflammasome complex formation and determine its structural features by cryogenic electron microscopy. We also provide a detailed understanding of how type III secretion system pathogen components are sensed by human NAIP to form a cascade of NLRC4 protomer through a critical lasso-like motif, a 'lock-key' activation model and large structural rearrangement, ultimately forming the full human NLRC4 inflammasome. These results shed light on key regulatory mechanisms specific to the NLRC4 inflammasome assembly, and the innate immune modalities of pathogen sensing in humans.
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