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Yorodumi- PDB-9q85: PAM-bound Cas9-Cas1-Cas2-Csn2 supercomplex in the locked conforma... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9q85 | ||||||||||||||||||
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| Title | PAM-bound Cas9-Cas1-Cas2-Csn2 supercomplex in the locked conformation, Streptococcus thermophilus DGCC 7710 CRISPR3 system | ||||||||||||||||||
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Keywords | DNA BINDING PROTEIN / CIRSPR-Cas / spacer acquisition / Csn2 / Cas1 / Cas2 / CRISPR integrase | ||||||||||||||||||
| Function / homology | Function and homology informationmaintenance of CRISPR repeat elements / RNA endonuclease activity / DNA endonuclease activity / endonuclease activity / defense response to virus / Hydrolases; Acting on ester bonds / hydrolase activity / DNA binding / RNA binding / metal ion binding Similarity search - Function | ||||||||||||||||||
| Biological species | Streptococcus thermophilus DGCC 7710 (bacteria)synthetic construct (others) | ||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.62 Å | ||||||||||||||||||
Authors | Sasnauskas, G. / Gaizauskaite, U. / Tamulaitiene, G. | ||||||||||||||||||
| Funding support | Lithuania, 1items
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Citation | Journal: Mol Cell / Year: 2026Title: Structural insights into Cas9-mediated prespacer selection in CRISPR-Cas adaptation. Authors: Ugne Gaizauskaite / Giedre Tamulaitiene / Arunas Silanskas / Giedrius Gasiunas / Virginijus Siksnys / Giedrius Sasnauskas Abstract: During CRISPR-Cas adaptation, prokaryotic cells become immunized by the insertion of foreign DNA fragments, termed spacers, into the host genome to serve as templates for RNA-guided immunity. Spacer ...During CRISPR-Cas adaptation, prokaryotic cells become immunized by the insertion of foreign DNA fragments, termed spacers, into the host genome to serve as templates for RNA-guided immunity. Spacer acquisition relies on the Cas1-Cas2 integrase and accessory proteins, which select DNA sequences flanked by the protospacer adjacent motif (PAM) and insert them into the CRISPR array. It has been shown that in type II-A systems, selection of PAM-proximal prespacers is mediated by the effector nuclease Cas9, which forms a "supercomplex" with the Cas1-Cas2 integrase and the Csn2 protein. Here, we present cryo-electron microscopy structures of the Streptococcus thermophilus type II-A prespacer selection supercomplex in the DNA-scanning and two distinct PAM-bound configurations, providing insights into the mechanism of Cas9-mediated prespacer selection in type II-A CRISPR-Cas systems. Repurposing Cas9 by the CRISPR adaptation machinery for prespacer selection, as characterized here, demonstrates Cas9 plasticity and expands our knowledge of Cas9 biology. | ||||||||||||||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 9q85.cif.gz | 565.2 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9q85.ent.gz | 419.5 KB | Display | PDB format |
| PDBx/mmJSON format | 9q85.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/q8/9q85 ftp://data.pdbj.org/pub/pdb/validation_reports/q8/9q85 | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 52886MC ![]() 8pj9C ![]() 9h1hC ![]() 9h1vC ![]() 9h21C ![]() 9h2gC ![]() 9h2mC ![]() 9h6tC ![]() 9h72C ![]() 9hp8C ![]() 9hp9C C: citing same article ( M: map data used to model this data |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
-CRISPR-associated ... , 4 types, 8 molecules AFGIOLNM
| #1: Protein | Mass: 162498.531 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Streptococcus thermophilus DGCC 7710 (bacteria)Gene: cas9, csn1 / Production host: ![]() References: UniProt: G3ECR1, Hydrolases; Acting on ester bonds | ||||
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| #6: Protein | Mass: 34854.875 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Details: C-terminal Histag Source: (gene. exp.) Streptococcus thermophilus DGCC 7710 (bacteria)Gene: cas1 / Production host: ![]() References: UniProt: G3ECR2, Hydrolases; Acting on ester bonds #7: Protein | | Mass: 13431.560 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Streptococcus thermophilus DGCC 7710 (bacteria)Gene: cas2 / Production host: ![]() References: UniProt: G3ECR3, Hydrolases; Acting on ester bonds #8: Protein | Mass: 27459.561 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Streptococcus thermophilus DGCC 7710 (bacteria)Gene: csn2 / Production host: ![]() |
-RNA chain , 2 types, 2 molecules BC
| #2: RNA chain | Mass: 13609.083 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
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| #3: RNA chain | Mass: 24119.357 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
-DNA chain , 2 types, 2 molecules DE
| #4: DNA chain | Mass: 15003.586 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
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| #5: DNA chain | Mass: 15182.787 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
-Non-polymers , 1 types, 1 molecules 
| #9: Chemical | ChemComp-CA / |
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-Details
| Has ligand of interest | N |
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| Has protein modification | N |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: PAM-bound Cas9-Cas1-Cas2-Csn2 supercomplex in the locked conformation, Streptococcus thermophilus DGCC 7710 CRISPR3 system Type: COMPLEX / Entity ID: #1-#8 / Source: RECOMBINANT |
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| Molecular weight | Experimental value: NO |
| Source (natural) | Organism: Streptococcus thermophilus DGCC 7710 (bacteria) |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.5 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Specimen support | Grid material: COPPER / Grid mesh size: 300 divisions/in. / Grid type: Quantifoil R1.2/1.3 |
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE |
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Electron microscopy imaging
| Microscopy | Model: TFS GLACIOS |
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| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: OTHER |
| Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 92000 X / Nominal defocus max: 2000 nm / Nominal defocus min: 1000 nm / Cs: 2.7 mm / C2 aperture diameter: 50 µm |
| Specimen holder | Cryogen: NITROGEN |
| Image recording | Average exposure time: 46.33 sec. / Electron dose: 30 e/Å2 / Detector mode: COUNTING / Film or detector model: FEI FALCON III (4k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||
| Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||
| 3D reconstruction | Resolution: 3.62 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 24394 / Algorithm: FOURIER SPACE / Symmetry type: POINT | ||||||||||||
| Atomic model building | PDB-ID: 9h2g Accession code: 9h2g / Source name: PDB / Type: experimental model | ||||||||||||
| Refinement | Cross valid method: NONE |
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Streptococcus thermophilus DGCC 7710 (bacteria)
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FIELD EMISSION GUN