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Yorodumi- EMDB-3088: Structural basis for DNA strand separation by a hexameric replica... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-3088 | |||||||||
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Title | Structural basis for DNA strand separation by a hexameric replicative helicase | |||||||||
Map data | Non-symmetrised reconstruction of full length E1 helices from bovine papillomavirus | |||||||||
Sample |
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Keywords | papillomavirus / helicase / DNA replication fork / electron microscopy / structural analysis | |||||||||
Function / homology | Function and homology information DNA helicase activity / DNA replication / DNA helicase / host cell nucleus / ATP hydrolysis activity / DNA binding / ATP binding Similarity search - Function | |||||||||
Biological species | Bovine papillomavirus | |||||||||
Method | single particle reconstruction / negative staining / Resolution: 23.0 Å | |||||||||
Authors | Chaban Y / Stead JA / Ryzhenkova K / Whelan F / Lamber K / Antson A / Sanders CM / Orlova EV | |||||||||
Citation | Journal: Nucleic Acids Res / Year: 2015 Title: Structural basis for DNA strand separation by a hexameric replicative helicase. Authors: Yuriy Chaban / Jonathan A Stead / Ksenia Ryzhenkova / Fiona Whelan / Ekaterina P Lamber / Alfred Antson / Cyril M Sanders / Elena V Orlova / Abstract: Hexameric helicases are processive DNA unwinding machines but how they engage with a replication fork during unwinding is unknown. Using electron microscopy and single particle analysis we determined ...Hexameric helicases are processive DNA unwinding machines but how they engage with a replication fork during unwinding is unknown. Using electron microscopy and single particle analysis we determined structures of the intact hexameric helicase E1 from papillomavirus and two complexes of E1 bound to a DNA replication fork end-labelled with protein tags. By labelling a DNA replication fork with streptavidin (dsDNA end) and Fab (5' ssDNA) we located the positions of these labels on the helicase surface, showing that at least 10 bp of dsDNA enter the E1 helicase via a side tunnel. In the currently accepted 'steric exclusion' model for dsDNA unwinding, the active 3' ssDNA strand is pulled through a central tunnel of the helicase motor domain as the dsDNA strands are wedged apart outside the protein assembly. Our structural observations together with nuclease footprinting assays indicate otherwise: strand separation is taking place inside E1 in a chamber above the helicase domain and the 5' passive ssDNA strands exits the assembly through a separate tunnel opposite to the dsDNA entry point. Our data therefore suggest an alternative to the current general model for DNA unwinding by hexameric helicases. | |||||||||
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_3088.map.gz | 1.3 MB | EMDB map data format | |
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Header (meta data) | emd-3088-v30.xml emd-3088.xml | 13.3 KB 13.3 KB | Display Display | EMDB header |
Images | emd_3088.png | 148.2 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-3088 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-3088 | HTTPS FTP |
-Validation report
Summary document | emd_3088_validation.pdf.gz | 193.2 KB | Display | EMDB validaton report |
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Full document | emd_3088_full_validation.pdf.gz | 192.4 KB | Display | |
Data in XML | emd_3088_validation.xml.gz | 5.4 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-3088 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-3088 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_3088.map.gz / Format: CCP4 / Size: 29.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Non-symmetrised reconstruction of full length E1 helices from bovine papillomavirus | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.6 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : Full-length E1 helicase-DNA complex
Entire | Name: Full-length E1 helicase-DNA complex |
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Components |
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-Supramolecule #1000: Full-length E1 helicase-DNA complex
Supramolecule | Name: Full-length E1 helicase-DNA complex / type: sample / ID: 1000 / Oligomeric state: hexamer / Number unique components: 1 |
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Molecular weight | Experimental: 410 KDa / Theoretical: 410 KDa / Method: Theoretical calculation |
-Macromolecule #1: Full-length hexameric E1 helicase
Macromolecule | Name: Full-length hexameric E1 helicase / type: protein_or_peptide / ID: 1 / Name.synonym: FLE1 / Number of copies: 6 / Oligomeric state: hexamer / Recombinant expression: Yes |
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Source (natural) | Organism: Bovine papillomavirus / synonym: Bovine papillomavirus / Organelle: nucleus / Location in cell: nucleus |
Molecular weight | Experimental: 410 KDa / Theoretical: 410 KDa |
Recombinant expression | Organism: Escherichia coli (E. coli) / Recombinant strain: BL21(DE3) / Recombinant plasmid: pET11c |
Sequence | UniProtKB: Replication protein E1 |
-Experimental details
-Structure determination
Method | negative staining |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 3 mg/mL |
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Buffer | pH: 8 Details: 10 mM Tris-Cl pH 8.0, 225 mM NaCl, 2 mM DTT, 0.1 mM PMSF, 0.1 mM EDTA |
Staining | Type: NEGATIVE / Details: Sample was stained with 2% uranyl acetate |
Grid | Details: Sample was applied on to carbon-coated copper grids (400 mesh, freshly glow-discharged in air) |
Vitrification | Cryogen name: NONE / Instrument: OTHER |
-Electron microscopy
Microscope | FEI TECNAI F20 |
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Temperature | Min: 291 K / Max: 296 K / Average: 293 K |
Alignment procedure | Legacy - Astigmatism: Objective lens astigmatism was corrected at 100,000 times magnification |
Date | Apr 15, 2012 |
Image recording | Category: CCD / Film or detector model: GATAN ULTRASCAN 4000 (4k x 4k) / Digitization - Sampling interval: 1.6 µm / Number real images: 45 / Average electron dose: 20 e/Å2 / Camera length: 1000 / Details: No subframe averaging was used. / Bits/pixel: 16 |
Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Calibrated magnification: 67000 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.1 mm / Nominal defocus max: 1.5 µm / Nominal defocus min: 0.5 µm / Nominal magnification: 62000 |
Sample stage | Specimen holder: Negative stain holder / Specimen holder model: OTHER |
Experimental equipment | Model: Tecnai F20 / Image courtesy: FEI Company |
+Image processing
-Atomic model buiding 1
Initial model | PDB ID: Chain - #0 - Chain ID: A / Chain - #1 - Chain ID: B / Chain - #2 - Chain ID: C / Chain - #3 - Chain ID: D / Chain - #4 - Chain ID: E / Chain - #5 - Chain ID: F |
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Software | Name: Chimera |
Details | The domains were separately fitted by manual docking using Chimera |
Refinement | Space: REAL / Protocol: RIGID BODY FIT / Target criteria: correlation coefficient |
-Atomic model buiding 2
Initial model | PDB ID: Chain - Chain ID: A |
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Software | Name: Chimera |
Details | The domains were separately fitted by manual docking using Chimera |
Refinement | Space: REAL / Protocol: RIGID BODY FIT / Target criteria: correlation coefficient |