+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-24258 | ||||||||||||||||||||||||
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Title | Structure of the in situ yeast NPC | ||||||||||||||||||||||||
Map data | full in situ NPC map recombined from 90 degree wedge focused alignment | ||||||||||||||||||||||||
Sample |
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Keywords | NPC / nucleocytoplasmic transport / TRANSLOCASE | ||||||||||||||||||||||||
Function / homology | Function and homology information response to spindle checkpoint signaling / nuclear pore linkers / peroxisomal importomer complex / regulation of protein desumoylation / mRNA export from nucleus in response to heat stress / nuclear pore inner ring / Seh1-associated complex / positive regulation of ER to Golgi vesicle-mediated transport / protein exit from endoplasmic reticulum / COPII-coated vesicle budding ...response to spindle checkpoint signaling / nuclear pore linkers / peroxisomal importomer complex / regulation of protein desumoylation / mRNA export from nucleus in response to heat stress / nuclear pore inner ring / Seh1-associated complex / positive regulation of ER to Golgi vesicle-mediated transport / protein exit from endoplasmic reticulum / COPII-coated vesicle budding / protein localization to nuclear inner membrane / chromosome, subtelomeric region / COPII-mediated vesicle transport / transcription-dependent tethering of RNA polymerase II gene DNA at nuclear periphery / nuclear pore localization / adenyl-nucleotide exchange factor activity / nuclear pore central transport channel / regulation of nucleocytoplasmic transport / establishment of mitotic spindle localization / nuclear migration along microtubule / regulation of TORC1 signaling / nuclear pore organization / nuclear pore outer ring / nuclear pore complex assembly / telomere tethering at nuclear periphery / COPII vesicle coat / post-transcriptional tethering of RNA polymerase II gene DNA at nuclear periphery / positive regulation of protein exit from endoplasmic reticulum / nuclear pore cytoplasmic filaments / Transport of Mature mRNA derived from an Intron-Containing Transcript / Regulation of HSF1-mediated heat shock response / nuclear pore nuclear basket / tRNA export from nucleus / SUMOylation of SUMOylation proteins / cytoplasmic dynein complex / protein localization to kinetochore / SUMOylation of RNA binding proteins / structural constituent of nuclear pore / SUMOylation of chromatin organization proteins / RNA export from nucleus / silent mating-type cassette heterochromatin formation / nucleocytoplasmic transport / vacuolar membrane / poly(A)+ mRNA export from nucleus / nuclear localization sequence binding / regulation of mitotic nuclear division / dynein intermediate chain binding / NLS-bearing protein import into nucleus / cytoplasmic microtubule / establishment of mitotic spindle orientation / Hydrolases; Acting on peptide bonds (peptidases); Serine endopeptidases / ribosomal large subunit export from nucleus / positive regulation of TOR signaling / subtelomeric heterochromatin formation / mRNA transport / mRNA export from nucleus / nuclear pore / ribosomal small subunit export from nucleus / ERAD pathway / Neutrophil degranulation / protein export from nucleus / positive regulation of TORC1 signaling / cellular response to amino acid starvation / nuclear periphery / cell periphery / chromosome segregation / promoter-specific chromatin binding / molecular condensate scaffold activity / heterochromatin formation / phospholipid binding / protein import into nucleus / transcription corepressor activity / double-strand break repair / protein transport / nuclear envelope / single-stranded DNA binding / cellular response to heat / nuclear membrane / amyloid fibril formation / chromosome, telomeric region / hydrolase activity / cell division / chromatin binding / endoplasmic reticulum membrane / protein-containing complex binding / positive regulation of DNA-templated transcription / structural molecule activity / negative regulation of transcription by RNA polymerase II / endoplasmic reticulum / positive regulation of transcription by RNA polymerase II / DNA binding / RNA binding / identical protein binding / nucleus / cytosol / cytoplasm Similarity search - Function | ||||||||||||||||||||||||
Biological species | Saccharomyces cerevisiae (brewer's yeast) | ||||||||||||||||||||||||
Method | subtomogram averaging / cryo EM / Resolution: 37.0 Å | ||||||||||||||||||||||||
Authors | Villa E / Singh D | ||||||||||||||||||||||||
Funding support | United States, 7 items
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Citation | Journal: Cell / Year: 2022 Title: Comprehensive structure and functional adaptations of the yeast nuclear pore complex. Authors: Christopher W Akey / Digvijay Singh / Christna Ouch / Ignacia Echeverria / Ilona Nudelman / Joseph M Varberg / Zulin Yu / Fei Fang / Yi Shi / Junjie Wang / Daniel Salzberg / Kangkang Song / ...Authors: Christopher W Akey / Digvijay Singh / Christna Ouch / Ignacia Echeverria / Ilona Nudelman / Joseph M Varberg / Zulin Yu / Fei Fang / Yi Shi / Junjie Wang / Daniel Salzberg / Kangkang Song / Chen Xu / James C Gumbart / Sergey Suslov / Jay Unruh / Sue L Jaspersen / Brian T Chait / Andrej Sali / Javier Fernandez-Martinez / Steven J Ludtke / Elizabeth Villa / Michael P Rout / Abstract: Nuclear pore complexes (NPCs) mediate the nucleocytoplasmic transport of macromolecules. Here we provide a structure of the isolated yeast NPC in which the inner ring is resolved by cryo-EM at sub- ...Nuclear pore complexes (NPCs) mediate the nucleocytoplasmic transport of macromolecules. Here we provide a structure of the isolated yeast NPC in which the inner ring is resolved by cryo-EM at sub-nanometer resolution to show how flexible connectors tie together different structural and functional layers. These connectors may be targets for phosphorylation and regulated disassembly in cells with an open mitosis. Moreover, some nucleoporin pairs and transport factors have similar interaction motifs, which suggests an evolutionary and mechanistic link between assembly and transport. We provide evidence for three major NPC variants that may foreshadow functional specializations at the nuclear periphery. Cryo-electron tomography extended these studies, providing a model of the in situ NPC with a radially expanded inner ring. Our comprehensive model reveals features of the nuclear basket and central transporter, suggests a role for the lumenal Pom152 ring in restricting dilation, and highlights structural plasticity that may be required for transport. | ||||||||||||||||||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_24258.map.gz | 76.1 MB | EMDB map data format | |
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Header (meta data) | emd-24258-v30.xml emd-24258.xml | 68.6 KB 68.6 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_24258_fsc.xml | 7.8 KB | Display | FSC data file |
Images | emd_24258.png | 197.2 KB | ||
Masks | emd_24258_msk_1.map emd_24258_msk_2.map emd_24258_msk_3.map | 34.3 MB 34.3 MB 34.3 MB | Mask map | |
Filedesc metadata | emd-24258.cif.gz | 18.9 KB | ||
Others | emd_24258_additional_1.map.gz emd_24258_additional_2.map.gz emd_24258_additional_3.map.gz emd_24258_additional_4.map.gz emd_24258_additional_5.map.gz emd_24258_additional_6.map.gz emd_24258_additional_7.map.gz emd_24258_half_map_1.map.gz emd_24258_half_map_2.map.gz | 111 MB 111.7 MB 113.8 MB 111.9 MB 111.8 MB 111.2 MB 112.2 MB 12.7 MB 12.8 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-24258 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-24258 | HTTPS FTP |
-Validation report
Summary document | emd_24258_validation.pdf.gz | 935 KB | Display | EMDB validaton report |
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Full document | emd_24258_full_validation.pdf.gz | 934.6 KB | Display | |
Data in XML | emd_24258_validation.xml.gz | 16.2 KB | Display | |
Data in CIF | emd_24258_validation.cif.gz | 20.4 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-24258 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-24258 | HTTPS FTP |
-Related structure data
Related structure data | 7n9fMC 7n84C 7n85C C: citing same article (ref.) M: atomic model generated by this map |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_24258.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | full in situ NPC map recombined from 90 degree wedge focused alignment | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 6.74 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
+Mask #1
+Mask #2
+Mask #3
+Additional map: zoned 3D map of Nsp1-FG-connections
+Additional map: zoned 3D map of inner ring of spokes
+Additional map: full in situ NPC map recombined from 90...
+Additional map: zoned 3D map of the N-ring
+Additional map: zoned 3D map of C-ring plus Nup82 complex with 3 Dyn 2 dimers
+Additional map: zoned 3D map of Pom152 ring
+Additional map: difference map for pore membrane
+Half map: half map
+Half map: half map
-Sample components
+Entire : yeast NPC
+Supramolecule #1: yeast NPC
+Macromolecule #1: Nucleoporin NUP170
+Macromolecule #2: Nucleoporin NUP157
+Macromolecule #3: orphans bound to Nup192 NTD
+Macromolecule #4: Nucleoporin NSP1
+Macromolecule #5: Nucleoporin NUP57
+Macromolecule #6: Nucleoporin NUP49/NSP49
+Macromolecule #7: Nucleoporin NUP192
+Macromolecule #8: Nucleoporin NUP188
+Macromolecule #9: Nucleoporin NIC96
+Macromolecule #10: Nucleoporin NUP53
+Macromolecule #11: Nucleoporin ASM4
+Macromolecule #12: Nucleoporin NUP82
+Macromolecule #13: Nucleoporin NUP159
+Macromolecule #14: Nucleoporin NUP120
+Macromolecule #15: Nucleoporin NUP85
+Macromolecule #16: Nucleoporin 145c
+Macromolecule #17: Protein transport protein SEC13
+Macromolecule #18: Nucleoporin SEH1
+Macromolecule #19: Nucleoporin NUP84
+Macromolecule #20: Nucleoporin NUP133
+Macromolecule #21: Dynein light chain 1, cytoplasmic
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | subtomogram averaging |
Aggregation state | cell |
-Sample preparation
Buffer | pH: 7.5 |
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Grid | Model: Quantifoil R2/1 / Material: COPPER / Mesh: 200 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec. / Pretreatment - Pressure: 0.039 kPa |
Vitrification | Cryogen name: ETHANE-PROPANE Details: A custom-built vitrification device (Max Planck Institute for Biochemistry, Munich). |
Details | W303 yeast cells were harvested during log-phase growth and diluted to an 0.8 x 107 cells/mL in YPD media. Five uL of this diluted sample was applied to glow-discharged 200-mesh, Quantafoil R2/1 grids (Electron Microscopy Sciences), excess media was manually blotted from the grid back side (opposite to the carbon substrate where the cells were deposited) and the grid was plunge frozen in a liquid ethane-propane mixture (50/50 volume, Airgas) then cryogenic, FIB milling was performed in an Aquilos DualBeam (Thermo Fisher Scientific) |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Energy filter - Name: GIF Quantum LS / Energy filter - Slit width: 20 eV |
Details | Tilt series collection: dose-symmetric & bi-directional |
Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Digitization - Dimensions - Width: 3838 pixel / Digitization - Dimensions - Height: 3708 pixel / Average exposure time: 2.0 sec. / Average electron dose: 4.5 e/Å2 Details: Images were collected in movie-mode at ~8 frames per second |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Calibrated defocus max: 6.0 µm / Calibrated defocus min: 2.5 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 6.0 µm / Nominal defocus min: 2.5 µm / Nominal magnification: 42000 |
Sample stage | Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
+Image processing
-Atomic model buiding 1
Details | Manual docking and limited molecular dynamics flexible fitting |
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Refinement | Space: REAL / Protocol: FLEXIBLE FIT / Target criteria: cross-correlation |
Output model | PDB-7n9f: |