+Open data
-Basic information
Entry | Database: PDB / ID: 8fvu | ||||||
---|---|---|---|---|---|---|---|
Title | Cryo-EM structure of human Needle/NAIP/NLRC4 (R288A) | ||||||
Components |
| ||||||
Keywords | IMMUNE SYSTEM / NLRC4 / NAIP / Inflammasome | ||||||
Function / homology | Function and homology information anthrax lethal factor endopeptidase / The IPAF inflammasome / IPAF inflammasome complex / icosanoid biosynthetic process / canonical inflammasome complex / type III protein secretion system complex / positive regulation of protein processing / caspase binding / protein secretion by the type III secretion system / activation of cysteine-type endopeptidase activity ...anthrax lethal factor endopeptidase / The IPAF inflammasome / IPAF inflammasome complex / icosanoid biosynthetic process / canonical inflammasome complex / type III protein secretion system complex / positive regulation of protein processing / caspase binding / protein secretion by the type III secretion system / activation of cysteine-type endopeptidase activity / pattern recognition receptor signaling pathway / host cell cytosol / cysteine-type endopeptidase inhibitor activity / TP53 Regulates Transcription of Caspase Activators and Caspases / pyroptotic inflammatory response / cysteine-type endopeptidase inhibitor activity involved in apoptotic process / Uptake and function of anthrax toxins / endopeptidase activator activity / negative regulation of tumor necrosis factor-mediated signaling pathway / 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 / negative regulation of cysteine-type endopeptidase activity involved in apoptotic process / protein homooligomerization / metalloendopeptidase activity / positive regulation of inflammatory response / metallopeptidase activity / activation of cysteine-type endopeptidase activity involved in apoptotic process / nervous system development / positive regulation of NF-kappaB transcription factor activity / toxin activity / basolateral plasma membrane / regulation of apoptotic process / negative regulation of neuron apoptotic process / defense response to bacterium / inflammatory response / positive regulation of apoptotic process / intracellular membrane-bounded organelle / innate immune response / apoptotic process / negative regulation of apoptotic process / cell surface / magnesium ion binding / protein homodimerization activity / ATP hydrolysis activity / proteolysis / zinc ion binding / extracellular region / ATP binding / identical protein binding / metal ion binding / plasma membrane / cytoplasm / cytosol Similarity search - Function | ||||||
Biological species | Homo sapiens (human) Bacillus anthracis (anthrax bacterium) Burkholderia (bacteria) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.6 Å | ||||||
Authors | Matico, R.E. / Yu, X. / Miller, R. / Somani, S. / Ricketts, M.D. / Kumar, N. / Steele, R.A. / Medley, Q. / Berger, S. / Faustin, B. / Sharma, S. | ||||||
Funding support | 1items
| ||||||
Citation | 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. | ||||||
History |
|
-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
---|
-Downloads & links
-Download
PDBx/mmCIF format | 8fvu.cif.gz | 492.8 KB | Display | PDBx/mmCIF format |
---|---|---|---|---|
PDB format | pdb8fvu.ent.gz | 384 KB | Display | PDB format |
PDBx/mmJSON format | 8fvu.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8fvu_validation.pdf.gz | 1.4 MB | Display | wwPDB validaton report |
---|---|---|---|---|
Full document | 8fvu_full_validation.pdf.gz | 1.4 MB | Display | |
Data in XML | 8fvu_validation.xml.gz | 69.2 KB | Display | |
Data in CIF | 8fvu_validation.cif.gz | 105 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/fv/8fvu ftp://data.pdbj.org/pub/pdb/validation_reports/fv/8fvu | HTTPS FTP |
-Related structure data
Related structure data | 29493MC 8fw2C 8fw9C M: map data used to model this data C: citing same article (ref.) |
---|---|
Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
|
---|---|
1 |
|
-Components
#1: Protein | Mass: 160484.359 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: NAIP, BIRC1 / Production host: Spodoptera frugiperda (fall armyworm) / References: UniProt: Q13075 | ||
---|---|---|---|
#2: Protein | Mass: 116941.531 Da / Num. of mol.: 1 / Mutation: R288A Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: NLRC4, CARD12, CLAN, CLAN1, IPAF, UNQ6189/PRO20215 / Production host: Spodoptera frugiperda (fall armyworm) / References: UniProt: Q9NPP4 | ||
#3: Protein | Mass: 42830.836 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Bacillus anthracis (anthrax bacterium), (gene. exp.) Burkholderia (bacteria) Gene: lef, pXO1-107, BXA0172, GBAA_pXO1_0172, BPSS1548 / Production host: Spodoptera frugiperda (fall armyworm) References: UniProt: P15917, UniProt: Q63K18, anthrax lethal factor endopeptidase | ||
#4: Chemical | ChemComp-ATP / | ||
#5: Chemical | Has ligand of interest | Y | |
-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
---|---|
EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-Sample preparation
Component |
| ||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Source (natural) |
| ||||||||||||||||||||||||
Source (recombinant) |
| ||||||||||||||||||||||||
Buffer solution | pH: 7.5 | ||||||||||||||||||||||||
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | ||||||||||||||||||||||||
Vitrification | Cryogen name: ETHANE |
-Electron microscopy imaging
Microscopy | Model: TFS GLACIOS |
---|---|
Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2400 nm / Nominal defocus min: 1200 nm |
Image recording | Electron dose: 40 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) |
-Processing
CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
---|---|
3D reconstruction | Resolution: 3.6 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 106381 / Symmetry type: POINT |