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Yorodumi- EMDB-51154: CryoEM structure of Enterococcus italicus Csm-crRNA complex bound... -
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Basic information
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| Title | CryoEM structure of Enterococcus italicus Csm-crRNA complex bound to pNppA3 and AMPNPP | |||||||||
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Keywords | Type III-A CRISPR-Cas RNA-guided nuclease Endoribonuclease cyclic oligoadenylate synthetase HD nuclease / RNA BINDING PROTEIN | |||||||||
| Function / homology | Function and homology informationexonuclease activity / Transferases; Transferring phosphorus-containing groups; Nucleotidyltransferases / transferase activity / endonuclease activity / defense response to virus / Hydrolases; Acting on ester bonds / RNA binding / ATP binding Similarity search - Function | |||||||||
| Biological species | Enterococcus italicus DSM 15952 (bacteria) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.05 Å | |||||||||
Authors | Jungfer K / Jinek M | |||||||||
| Funding support | European Union, 1 items
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Citation | Journal: Nucleic Acids Res / Year: 2025Title: Mechanistic determinants and dynamics of cA6 synthesis in type III CRISPR-Cas effector complexes. Authors: Kenny Jungfer / Štefan Moravčík / Carmela Garcia-Doval / Anna Knörlein / Jonathan Hall / Martin Jinek / ![]() Abstract: Type III clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) systems (type III CRISPR-Cas systems) use guide RNAs to recognize RNA transcripts of foreign ...Type III clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) systems (type III CRISPR-Cas systems) use guide RNAs to recognize RNA transcripts of foreign genetic elements, which triggers the generation of cyclic oligoadenylate (cOA) second messengers by the Cas10 subunit of the type III effector complex. In turn, cOAs bind and activate ancillary effector proteins to reinforce the host immune response. Type III systems utilize distinct cOAs, including cyclic tri- (cA3), tetra- (cA4) and hexa-adenylates (cA6). However, the molecular mechanisms dictating cOA product identity are poorly understood. Here we used cryoelectron microscopy to visualize the mechanism of cA6 biosynthesis by the Csm effector complex from Enterococcus italicus (EiCsm). We show that EiCsm synthesizes oligoadenylate nucleotides in 3'-5' direction using a set of conserved binding sites in the Cas10 Palm domains to determine the size of the nascent oligoadenylate chain. Our data also reveal that conformational dynamics induced by target RNA binding results in allosteric activation of Cas10 to trigger oligoadenylate synthesis. Mutations of a key structural element in Cas10 perturb cOA synthesis to favor cA3 and cA4 formation. Together, these results provide comprehensive insights into the dynamics of cOA synthesis in type III CRISPR-Cas systems and reveal key determinants of second messenger product selectivity, thereby illuminating potential avenues for their engineering. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_51154.map.gz | 398.6 MB | EMDB map data format | |
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| Header (meta data) | emd-51154-v30.xml emd-51154.xml | 23.4 KB 23.4 KB | Display Display | EMDB header |
| Images | emd_51154.png | 32.4 KB | ||
| Filedesc metadata | emd-51154.cif.gz | 7.8 KB | ||
| Others | emd_51154_half_map_1.map.gz emd_51154_half_map_2.map.gz | 391.1 MB 391.1 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-51154 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-51154 | HTTPS FTP |
-Validation report
| Summary document | emd_51154_validation.pdf.gz | 1.2 MB | Display | EMDB validaton report |
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| Full document | emd_51154_full_validation.pdf.gz | 1.2 MB | Display | |
| Data in XML | emd_51154_validation.xml.gz | 18 KB | Display | |
| Data in CIF | emd_51154_validation.cif.gz | 21.3 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-51154 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-51154 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9g9jMC ![]() 9g9aC ![]() 9g9bC ![]() 9g9cC ![]() 9g9dC ![]() 9g9eC ![]() 9g9fC ![]() 9g9gC ![]() 9g9hC ![]() 9g9iC ![]() 9g9kC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_51154.map.gz / Format: CCP4 / Size: 421.9 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: 0.65 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #2
| File | emd_51154_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_51154_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
+Entire : Binary Csm-crRNA complex bound to pNppA3 and AMPPNP with (Csm1)1(...
+Supramolecule #1: Binary Csm-crRNA complex bound to pNppA3 and AMPPNP with (Csm1)1(...
+Macromolecule #1: CRISPR system single-strand-specific deoxyribonuclease Cas10/Csm1...
+Macromolecule #2: CRISPR system Cms protein Csm2
+Macromolecule #3: CRISPR system Cms endoribonuclease Csm3
+Macromolecule #4: CRISPR system Cms protein Csm4
+Macromolecule #5: CRISPR system Cms protein Csm5
+Macromolecule #6: crRNA
+Macromolecule #7: adenosine-5'-[(beta,gamma)-imido]triphosphate-adenosine-monophosp...
+Macromolecule #8: PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER
+Macromolecule #9: MANGANESE (II) ION
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 1 mg/mL | |||||||||||||||
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| Buffer | pH: 7.5 Component:
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| Grid | Model: Quantifoil R1.2/1.3 / Material: GOLD / Mesh: 200 | |||||||||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277.14 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 66.51 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.4 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 130000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
| Startup model | Type of model: NONE |
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| Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 3.05 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 53176 |
| Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
| Final angle assignment | Type: MAXIMUM LIKELIHOOD |
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Keywords
Enterococcus italicus DSM 15952 (bacteria)
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FIELD EMISSION GUN
