+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-3032 | |||||||||
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Title | Cryo-EM structure of ATP-bound IstB | |||||||||
Map data | IstB decamer bound to ATP | |||||||||
Sample |
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Keywords | AAA+ / ATPase / IS21 / DNA transposition / DNA binding / DNA remodeling | |||||||||
Biological species | Geobacillus stearothermophilus (bacteria) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 16.0 Å | |||||||||
Authors | Arias-Palomo E / Berger JM | |||||||||
Citation | Journal: Cell / Year: 2015 Title: An Atypical AAA+ ATPase Assembly Controls Efficient Transposition through DNA Remodeling and Transposase Recruitment. Authors: Ernesto Arias-Palomo / James M Berger / Abstract: Transposons are ubiquitous genetic elements that drive genome rearrangements, evolution, and the spread of infectious disease and drug-resistance. Many transposons, such as Mu, Tn7, and IS21, require ...Transposons are ubiquitous genetic elements that drive genome rearrangements, evolution, and the spread of infectious disease and drug-resistance. Many transposons, such as Mu, Tn7, and IS21, require regulatory AAA+ ATPases for function. We use X-ray crystallography and cryo-electron microscopy to show that the ATPase subunit of IS21, IstB, assembles into a clamshell-shaped decamer that sandwiches DNA between two helical pentamers of ATP-associated AAA+ domains, sharply bending the duplex into a 180° U-turn. Biochemical studies corroborate key features of the structure and further show that the IS21 transposase, IstA, recognizes the IstB•DNA complex and promotes its disassembly by stimulating ATP hydrolysis. Collectively, these studies reveal a distinct manner of higher-order assembly and client engagement by a AAA+ ATPase and suggest a mechanistic model where IstB binding and subsequent DNA bending primes a selected insertion site for efficient transposition. | |||||||||
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_3032.map.gz | 705 KB | EMDB map data format | |
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Header (meta data) | emd-3032-v30.xml emd-3032.xml | 8 KB 8 KB | Display Display | EMDB header |
Images | emd_3032.png | 316.9 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-3032 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-3032 | HTTPS FTP |
-Validation report
Summary document | emd_3032_validation.pdf.gz | 186.6 KB | Display | EMDB validaton report |
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Full document | emd_3032_full_validation.pdf.gz | 185.7 KB | Display | |
Data in XML | emd_3032_validation.xml.gz | 5.4 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-3032 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-3032 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_3032.map.gz / Format: CCP4 / Size: 11.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | IstB decamer bound to ATP | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 2.05 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 : ATP-bound IstB decamer
Entire | Name: ATP-bound IstB decamer |
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Components |
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-Supramolecule #1000: ATP-bound IstB decamer
Supramolecule | Name: ATP-bound IstB decamer / type: sample / ID: 1000 / Details: The sample was monodisperse Oligomeric state: IstB oligomerizes into pentamer of dimers when bound to ATP Number unique components: 1 |
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Molecular weight | Experimental: 290 KDa / Theoretical: 290 KDa / Method: Analytical size exclusion chromatography |
-Macromolecule #1: IstB
Macromolecule | Name: IstB / type: protein_or_peptide / ID: 1 / Number of copies: 10 / Recombinant expression: Yes |
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Source (natural) | Organism: Geobacillus stearothermophilus (bacteria) |
Molecular weight | Theoretical: 29 KDa |
Recombinant expression | Organism: Escherichia coli (E. coli) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 2 mg/mL |
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Buffer | pH: 7.5 Details: 20 mM HEPES pH 7.5, 300 mM NaCl, 5 mM MgCl2, 1.5% glycerol, 1 mM DTT, 1 mM ATP |
Grid | Details: C-Flat 400 mesh 2/2. Open holes |
Vitrification | Cryogen name: ETHANE / Instrument: FEI VITROBOT MARK II / Method: Blot for 4 seconds before plunging |
-Electron microscopy
Microscope | FEI TECNAI F20 |
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Date | Jun 12, 2013 |
Image recording | Category: CCD / Film or detector model: GATAN ULTRASCAN 4000 (4k x 4k) / Average electron dose: 20 e/Å2 |
Electron beam | Acceleration voltage: 120 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.5 µm / Nominal defocus min: 1.3 µm / Nominal magnification: 100000 |
Sample stage | Specimen holder model: GATAN LIQUID NITROGEN |
Experimental equipment | Model: Tecnai F20 / Image courtesy: FEI Company |
-Image processing
CTF correction | Details: Each micrograph |
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Final reconstruction | Applied symmetry - Point group: C2 (2 fold cyclic) / Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 16.0 Å / Resolution method: OTHER / Software - Name: EMAN2, SPARX / Number images used: 34064 |