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Open data
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Basic information
Entry | Database: PDB / ID: 8sxn | ||||||
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Title | Structure of NLRP3 and NEK7 complex | ||||||
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![]() | IMMUNE SYSTEM / NLRP3 NEK7 complex / Cryo-EM | ||||||
Function / homology | ![]() NEK6-subfamily protein kinase / detection of biotic stimulus / molecular sensor activity / phosphatidylinositol phosphate binding / Activation of NIMA Kinases NEK9, NEK6, NEK7 / positive regulation of T-helper 2 cell differentiation / NLRP3 inflammasome complex assembly / positive regulation of T-helper 2 cell cytokine production / interphase microtubule organizing center / positive regulation of type 2 immune response ...NEK6-subfamily protein kinase / detection of biotic stimulus / molecular sensor activity / phosphatidylinositol phosphate binding / Activation of NIMA Kinases NEK9, NEK6, NEK7 / positive regulation of T-helper 2 cell differentiation / NLRP3 inflammasome complex assembly / positive regulation of T-helper 2 cell cytokine production / interphase microtubule organizing center / positive regulation of type 2 immune response / NLRP3 inflammasome complex / Nuclear Pore Complex (NPC) Disassembly / cysteine-type endopeptidase activator activity / peptidoglycan binding / cellular response to potassium ion / osmosensory signaling pathway / phosphatidylinositol-4-phosphate binding / negative regulation of non-canonical NF-kappaB signal transduction / pattern recognition receptor signaling pathway / negative regulation of interleukin-1 beta production / positive regulation of NLRP3 inflammasome complex assembly / pyroptotic inflammatory response / positive regulation of interleukin-4 production / positive regulation of telomere maintenance / microtubule organizing center / negative regulation of acute inflammatory response / The NLRP3 inflammasome / Purinergic signaling in leishmaniasis infection / spindle assembly / signaling adaptor activity / EML4 and NUDC in mitotic spindle formation / protein maturation / regulation of mitotic cell cycle / molecular function activator activity / positive regulation of interleukin-1 beta production / molecular condensate scaffold activity / defense response / positive regulation of non-canonical NF-kappaB signal transduction / Cytoprotection by HMOX1 / ADP binding / protein homooligomerization / cellular response to virus / Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement / negative regulation of inflammatory response / Metalloprotease DUBs / positive regulation of inflammatory response / spindle pole / positive regulation of NF-kappaB transcription factor activity / SARS-CoV-1 activates/modulates innate immune responses / cellular response to lipopolysaccharide / regulation of inflammatory response / protein-macromolecule adaptor activity / DNA-binding transcription factor binding / molecular adaptor activity / sequence-specific DNA binding / microtubule / eukaryotic translation initiation factor 2alpha kinase activity / 3-phosphoinositide-dependent protein kinase activity / DNA-dependent protein kinase activity / ribosomal protein S6 kinase activity / histone H3S10 kinase activity / histone H2AXS139 kinase activity / histone H3S28 kinase activity / histone H4S1 kinase activity / histone H2BS14 kinase activity / histone H3T3 kinase activity / histone H2AS121 kinase activity / Rho-dependent protein serine/threonine kinase activity / histone H2BS36 kinase activity / histone H3S57 kinase activity / histone H2AT120 kinase activity / AMP-activated protein kinase activity / histone H2AS1 kinase activity / histone H3T6 kinase activity / histone H3T11 kinase activity / histone H3T45 kinase activity / protein phosphorylation / inflammatory response / Golgi membrane / innate immune response / protein serine kinase activity / protein serine/threonine kinase activity / apoptotic process / centrosome / SARS-CoV-2 activates/modulates innate and adaptive immune responses / endoplasmic reticulum / signal transduction / positive regulation of transcription by RNA polymerase II / ATP hydrolysis activity / mitochondrion / extracellular region / nucleoplasm / ATP binding / metal ion binding / identical protein binding / nucleus / membrane / cytosol / cytoplasm Similarity search - Function | ||||||
Biological species | ![]() | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 4.04 Å | ||||||
![]() | Yu, X. / Matico, R.E. / Miller, R. / Schoubroeck, B.V. / Grauwen, K. / Suarez, J. / Pietrak, B. / Haloi, N. / Yin, Y. / Tresadern, G.J. ...Yu, X. / Matico, R.E. / Miller, R. / Schoubroeck, B.V. / Grauwen, K. / Suarez, J. / Pietrak, B. / Haloi, N. / Yin, Y. / Tresadern, G.J. / Perez-Benito, L. / Lindahl, E. / Bottelbergs, A. / Oehlrich, D. / Opdenbosch, N.V. / Sharma, S. | ||||||
Funding support | 1items
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![]() | ![]() Title: Cryo-EM structures of NLRP3 reveal its self-activation mechanism Authors: Yu, X. / Matico, R.E. / Miller, R. / Schoubroeck, B.V. / Grauwen, K. / Suarez, J. / Pietrak, B. / Haloi, N. / Yin, Y. / Tresadern, G.J. / Perez-Benito, L. / Lindahl, E. / Bottelbergs, A. / ...Authors: Yu, X. / Matico, R.E. / Miller, R. / Schoubroeck, B.V. / Grauwen, K. / Suarez, J. / Pietrak, B. / Haloi, N. / Yin, Y. / Tresadern, G.J. / Perez-Benito, L. / Lindahl, E. / Bottelbergs, A. / Oehlrich, D. / Opdenbosch, N.V. / Sharma, S. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 452.7 KB | Display | ![]() |
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PDB format | ![]() | 361.4 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
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-Related structure data
Related structure data | ![]() 40855MC ![]() 8swfC ![]() 8swkC M: map data used to model this data C: citing same article ( |
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Similar structure data | Similarity search - Function & homology ![]() |
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Links
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Assembly
Deposited unit | ![]()
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Components
#1: Protein | Mass: 34603.004 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() #2: Protein | Mass: 103676.641 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() References: UniProt: Q96P20, Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement #3: Chemical | #4: Chemical | Has ligand of interest | Y | |
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-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
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EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
Component | Name: Covid Spike variant deltaN135 / Type: COMPLEX / Entity ID: #1 / Source: RECOMBINANT |
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Source (natural) | Organism: ![]() ![]() |
Source (recombinant) | Organism: ![]() |
Buffer solution | pH: 7.5 |
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Microscopy | Model: FEI TITAN KRIOS |
Electron gun | Electron source: ![]() |
Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2400 nm / Nominal defocus min: 1400 nm |
Image recording | Electron dose: 52 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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3D reconstruction | Resolution: 4.04 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 199924 / Symmetry type: POINT |