+Open data
-Basic information
Entry | Database: PDB / ID: 8sfj | ||||||
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Title | WT CRISPR-Cas12a with a 10bp R-loop | ||||||
Components |
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Keywords | DNA BINDING PROTEIN/DNA/RNA / CRISPR / R-loop / endonuclease / DNA BINDING PROTEIN / DNA BINDING PROTEIN-DNA-RNA complex | ||||||
Function / homology | Function and homology information Bacillus subtilis ribonuclease / : / deoxyribonuclease I / deoxyribonuclease I activity / defense response to virus / lyase activity / DNA binding / RNA binding Similarity search - Function | ||||||
Biological species | Acidaminococcus sp. BV3L6 (bacteria) synthetic construct (others) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.6 Å | ||||||
Authors | Strohkendl, I. / Taylor, D.W. | ||||||
Funding support | United States, 1items
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Citation | Journal: To Be Published Title: WT CRISPR-Cas12a with a 10bp R-loop Authors: Strohkendl, I. / Taylor, D.W. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 8sfj.cif.gz | 250.7 KB | Display | PDBx/mmCIF format |
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PDB format | pdb8sfj.ent.gz | 186.2 KB | Display | PDB format |
PDBx/mmJSON format | 8sfj.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8sfj_validation.pdf.gz | 1.1 MB | Display | wwPDB validaton report |
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Full document | 8sfj_full_validation.pdf.gz | 1.1 MB | Display | |
Data in XML | 8sfj_validation.xml.gz | 42.5 KB | Display | |
Data in CIF | 8sfj_validation.cif.gz | 62.1 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/sf/8sfj ftp://data.pdbj.org/pub/pdb/validation_reports/sf/8sfj | HTTPS FTP |
-Related structure data
Related structure data | 40443MC 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: 151705.234 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Acidaminococcus sp. BV3L6 (bacteria) / Gene: cas12a, cpf1, HMPREF1246_0236 / Production host: Escherichia coli BL21(DE3) (bacteria) References: UniProt: U2UMQ6, deoxyribonuclease I, Bacillus subtilis ribonuclease |
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#2: RNA chain | Mass: 15351.995 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
#3: DNA chain | Mass: 17211.082 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
#4: DNA chain | Mass: 17299.061 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
-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: WT AsCas12a incubated with 12bp-complementary target DNA Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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Source (natural) | Organism: Acidaminococcus sp. BV3L6 (bacteria) |
Source (recombinant) | Organism: Escherichia coli BL21(DE3) (bacteria) |
Buffer solution | pH: 7 |
Specimen | Conc.: 1 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 277 K |
-Electron microscopy imaging
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
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Microscopy | Model: TFS 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: 1500 nm |
Image recording | Electron dose: 80 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
-Processing
EM software |
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CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
3D reconstruction | Resolution: 3.6 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 122723 / Symmetry type: POINT | ||||||||||||||||||||||||
Refinement | Cross valid method: NONE Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2 | ||||||||||||||||||||||||
Displacement parameters | Biso mean: 224.14 Å2 | ||||||||||||||||||||||||
Refine LS restraints |
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