+Open data
-Basic information
Entry | Database: PDB / ID: 7yn9 | ||||||
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Title | Cryo-EM structure of Cas7-11-crRNA binary complex | ||||||
Components |
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Keywords | RNA BINDING PROTEIN / Cas7-11 / crRNA / CRISPR-Cas / Csx29 | ||||||
Function / homology | : / CRISPR type III-associated protein / RAMP superfamily / defense response to virus / RNA / RNA (> 10) / CRISPR-associated RAMP family protein Function and homology information | ||||||
Biological species | Desulfonema ishimotonii (bacteria) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.53 Å | ||||||
Authors | Huo, Y. / Dong, Q. / Zhao, H. / Jiang, T. | ||||||
Funding support | China, 1items
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Citation | Journal: Nat Microbiol / Year: 2023 Title: Cryo-EM structure and protease activity of the type III-E CRISPR-Cas effector. Authors: Yangao Huo / Hongshen Zhao / Qinghua Dong / Tao Jiang / Abstract: The recently discovered type III-E CRISPR-Cas effector Cas7-11 shows promise when used as an RNA manipulation tool, but its structure and the mechanisms underlying its function remain unclear. Here ...The recently discovered type III-E CRISPR-Cas effector Cas7-11 shows promise when used as an RNA manipulation tool, but its structure and the mechanisms underlying its function remain unclear. Here we present four cryo-EM structures of Desulfonema ishimotonii Cas7-11-crRNA complex in pre-target and target RNA-bound states, and the cryo-EM structure of DiCas7-11-crRNA bound to its accessory protein DiCsx29. These data reveal structural elements for pre-crRNA processing, target RNA cleavage and regulation. Moreover, a 3' seed region of crRNA is involved in regulating RNA cleavage activity of DiCas7-11-crRNA-Csx29. Our analysis also shows that both the minimal mismatch of 4 nt to the 5' handle of crRNA and the minimal matching of the first 12 nt of the spacer by the target RNA are essential for triggering the protease activity of DiCas7-11-crRNA-Csx29 towards DiCsx30. Taken together, we propose that target RNA recognition and cleavage regulate and fine-tune the protease activity of DiCas7-11-crRNA-Csx29, thus preventing auto-immune responses. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 7yn9.cif.gz | 304.5 KB | Display | PDBx/mmCIF format |
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PDB format | pdb7yn9.ent.gz | 237.2 KB | Display | PDB format |
PDBx/mmJSON format | 7yn9.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 7yn9_validation.pdf.gz | 1.2 MB | Display | wwPDB validaton report |
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Full document | 7yn9_full_validation.pdf.gz | 1.2 MB | Display | |
Data in XML | 7yn9_validation.xml.gz | 54.8 KB | Display | |
Data in CIF | 7yn9_validation.cif.gz | 81.5 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/yn/7yn9 ftp://data.pdbj.org/pub/pdb/validation_reports/yn/7yn9 | HTTPS FTP |
-Related structure data
Related structure data | 33955MC 7ynaC 7ynbC 7yncC 7yndC M: map data used to model this data C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
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1 |
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-Components
#1: Protein | Mass: 183933.000 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Desulfonema ishimotonii (bacteria) / Gene: DENIS_1082 / Production host: Escherichia coli (E. coli) / References: UniProt: A0A401FT36 |
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#2: RNA chain | Mass: 15094.032 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: 38-MER / Source: (gene. exp.) Desulfonema ishimotonii (bacteria) / Production host: Escherichia coli (E. coli) |
-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
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EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-Sample preparation
Component | Name: Cas7-11-crRNA binary complex / Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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Source (natural) | Organism: Desulfonema ishimotonii (bacteria) |
Source (recombinant) | Organism: Escherichia coli (E. coli) |
Buffer solution | pH: 7.5 |
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
Vitrification | Cryogen name: ETHANE |
-Electron microscopy imaging
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
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Microscopy | Model: FEI TITAN KRIOS |
Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2500 nm / Nominal defocus min: 1300 nm |
Image recording | Electron dose: 60 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
-Processing
Software |
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CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
3D reconstruction | Resolution: 3.53 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 292109 / Symmetry type: POINT | ||||||||||||||||||||||||
Refinement | Cross valid method: NONE Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2 | ||||||||||||||||||||||||
Displacement parameters | Biso mean: 62.05 Å2 | ||||||||||||||||||||||||
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