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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-8994 | |||||||||
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| Title | CasX-gRNA-DNA (30bp) State II | |||||||||
Map data | CasX-gRNA-DNA(30bp) state II | |||||||||
Sample |
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| Function / homology | Transposase Function and homology information | |||||||||
| Biological species | Deltaproteobacteria (d-proteobacteria) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 4.2 Å | |||||||||
Authors | Liu JJ / Orlova N | |||||||||
Citation | Journal: Nature / Year: 2019Title: CasX enzymes comprise a distinct family of RNA-guided genome editors. Authors: Jun-Jie Liu / Natalia Orlova / Benjamin L Oakes / Enbo Ma / Hannah B Spinner / Katherine L M Baney / Jonathan Chuck / Dan Tan / Gavin J Knott / Lucas B Harrington / Basem Al-Shayeb / ...Authors: Jun-Jie Liu / Natalia Orlova / Benjamin L Oakes / Enbo Ma / Hannah B Spinner / Katherine L M Baney / Jonathan Chuck / Dan Tan / Gavin J Knott / Lucas B Harrington / Basem Al-Shayeb / Alexander Wagner / Julian Brötzmann / Brett T Staahl / Kian L Taylor / John Desmarais / Eva Nogales / Jennifer A Doudna / ![]() Abstract: The RNA-guided CRISPR-associated (Cas) proteins Cas9 and Cas12a provide adaptive immunity against invading nucleic acids, and function as powerful tools for genome editing in a wide range of ...The RNA-guided CRISPR-associated (Cas) proteins Cas9 and Cas12a provide adaptive immunity against invading nucleic acids, and function as powerful tools for genome editing in a wide range of organisms. Here we reveal the underlying mechanisms of a third, fundamentally distinct RNA-guided genome-editing platform named CRISPR-CasX, which uses unique structures for programmable double-stranded DNA binding and cleavage. Biochemical and in vivo data demonstrate that CasX is active for Escherichia coli and human genome modification. Eight cryo-electron microscopy structures of CasX in different states of assembly with its guide RNA and double-stranded DNA substrates reveal an extensive RNA scaffold and a domain required for DNA unwinding. These data demonstrate how CasX activity arose through convergent evolution to establish an enzyme family that is functionally separate from both Cas9 and Cas12a. | |||||||||
| History |
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Structure visualization
| Movie |
Movie viewer |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_8994.map.gz | 59.5 MB | EMDB map data format | |
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| Header (meta data) | emd-8994-v30.xml emd-8994.xml | 8.4 KB 8.4 KB | Display Display | EMDB header |
| Images | emd_8994.png | 96.5 KB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-8994 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-8994 | HTTPS FTP |
-Validation report
| Summary document | emd_8994_validation.pdf.gz | 342.5 KB | Display | EMDB validaton report |
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| Full document | emd_8994_full_validation.pdf.gz | 342 KB | Display | |
| Data in XML | emd_8994_validation.xml.gz | 6.1 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-8994 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-8994 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 6ny1MC ![]() 8980C ![]() 8987C ![]() 8988C ![]() 8989C ![]() 8990C ![]() 8991C ![]() 8996C ![]() 6ny2C ![]() 6ny3C M: atomic model generated by this map C: citing same article ( |
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| Similar structure data |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_8994.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | CasX-gRNA-DNA(30bp) state II | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.9 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : CasX-gRNA-DNA (30bp) State II
| Entire | Name: CasX-gRNA-DNA (30bp) State II |
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| Components |
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-Supramolecule #1: CasX-gRNA-DNA (30bp) State II
| Supramolecule | Name: CasX-gRNA-DNA (30bp) State II / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4 |
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| Source (natural) | Organism: Deltaproteobacteria (d-proteobacteria) |
| Recombinant expression | Organism: ![]() |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.5 |
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| Grid | Details: unspecified |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Average electron dose: 46.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
| Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 4.2 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 105395 |
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| Initial angle assignment | Type: RANDOM ASSIGNMENT |
| Final angle assignment | Type: MAXIMUM LIKELIHOOD |
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