+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-31059 | |||||||||
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Title | The Csy-AcrIF14-dsDNA complex | |||||||||
Map data | ||||||||||
Sample |
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Keywords | inhibitor / complex / IMMUNE SYSTEM / IMMUNE SYSTEM-RNA-DNA complex | |||||||||
Function / homology | Function and homology information CRISPR-associated protein Csy1 / CRISPR-associated protein (Cas_Csy1) / CRISPR-associated protein Csy2 / CRISPR-associated protein (Cas_Csy2) / CRISPR-associated protein Csy3 / CRISPR-associated protein (Cas_Csy3) Similarity search - Domain/homology | |||||||||
Biological species | Pseudomonas aeruginosa (bacteria) / Moraxella phage Mcat5 (virus) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.1 Å | |||||||||
Authors | Zhang LX / Feng Y | |||||||||
Funding support | China, 1 items
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Citation | Journal: Nucleic Acids Res / Year: 2021 Title: Insights into the dual functions of AcrIF14 during the inhibition of type I-F CRISPR-Cas surveillance complex. Authors: Xi Liu / Laixing Zhang / Yu Xiu / Teng Gao / Ling Huang / Yongchao Xie / Lingguang Yang / Wenhe Wang / Peiyi Wang / Yi Zhang / Maojun Yang / Yue Feng / Abstract: CRISPR-Cas systems are bacterial adaptive immune systems, and phages counteract these systems using many approaches such as producing anti-CRISPR (Acr) proteins. Here, we report the structures of ...CRISPR-Cas systems are bacterial adaptive immune systems, and phages counteract these systems using many approaches such as producing anti-CRISPR (Acr) proteins. Here, we report the structures of both AcrIF14 and its complex with the crRNA-guided surveillance (Csy) complex. Our study demonstrates that apart from interacting with the Csy complex to block the hybridization of target DNA to the crRNA, AcrIF14 also endows the Csy complex with the ability to interact with non-sequence-specific dsDNA as AcrIF9 does. Further structural studies of the Csy-AcrIF14-dsDNA complex and biochemical studies uncover that the PAM recognition loop of the Cas8f subunit of the Csy complex and electropositive patches within the N-terminal domain of AcrIF14 are essential for the non-sequence-specific dsDNA binding to the Csy-AcrIF14 complex, which is different from the mechanism of AcrIF9. Our findings highlight the prevalence of Acr-induced non-specific DNA binding and shed light on future studies into the mechanisms of such Acr proteins. | |||||||||
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_31059.map.gz | 5.7 MB | EMDB map data format | |
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Header (meta data) | emd-31059-v30.xml emd-31059.xml | 17.5 KB 17.5 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_31059_fsc.xml | 8.6 KB | Display | FSC data file |
Images | emd_31059.png | 99 KB | ||
Filedesc metadata | emd-31059.cif.gz | 6.3 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-31059 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-31059 | HTTPS FTP |
-Validation report
Summary document | emd_31059_validation.pdf.gz | 437.1 KB | Display | EMDB validaton report |
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Full document | emd_31059_full_validation.pdf.gz | 436.7 KB | Display | |
Data in XML | emd_31059_validation.xml.gz | 10.4 KB | Display | |
Data in CIF | emd_31059_validation.cif.gz | 13.6 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-31059 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-31059 | HTTPS FTP |
-Related structure data
Related structure data | 7ecwMC 7du0C 7ecvC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_31059.map.gz / Format: CCP4 / Size: 52.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.1 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 : membrane protein
+Supramolecule #1: membrane protein
+Supramolecule #2: membrane protein
+Supramolecule #3: AcrIF14
+Macromolecule #1: Type I-F CRISPR-associated protein Csy1
+Macromolecule #2: CRISPR type I-F/YPEST-associated protein Csy2
+Macromolecule #3: CRISPR-associated protein Csy3
+Macromolecule #4: AcrIF14
+Macromolecule #5: RNA (60-MER)
+Macromolecule #6: 54-MER DNA
+Macromolecule #7: 54-MER DNA
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: OTHER / Imaging mode: DARK FIELD |