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Yorodumi- EMDB-51812: Cas9:crRNA:tracrRNA in complex with PAM-containing non-cognate DN... -
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Basic information
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| Title | Cas9:crRNA:tracrRNA in complex with PAM-containing non-cognate DNA, PAM-unbound conformation, Streptococcus thermophilus DGCC 7710 CRISPR3 system | |||||||||
Map data | Unsharpened map | |||||||||
Sample |
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Keywords | Cas9 / PAM / CRISPR-Cas / RNA BINDING PROTEIN / DNA BINDING PROTEIN | |||||||||
| Function / homology | Function and homology informationmaintenance of CRISPR repeat elements / 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 | single particle reconstruction / cryo EM / Resolution: 3.06 Å | |||||||||
Authors | Sasnauskas G / Gaizauskaite U / Tamulaitiene G | |||||||||
| Funding support | Lithuania, 1 items
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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
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Downloads & links
-EMDB archive
| Map data | emd_51812.map.gz | 15.1 MB | EMDB map data format | |
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| Header (meta data) | emd-51812-v30.xml emd-51812.xml | 29.1 KB 29.1 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_51812_fsc.xml | 9.1 KB | Display | FSC data file |
| Images | emd_51812.png | 145.5 KB | ||
| Masks | emd_51812_msk_1.map | 30.5 MB | Mask map | |
| Filedesc metadata | emd-51812.cif.gz | 8 KB | ||
| Others | emd_51812_additional_1.map.gz emd_51812_half_map_1.map.gz emd_51812_half_map_2.map.gz | 27.8 MB 28.2 MB 28.2 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-51812 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-51812 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9h2mMC ![]() 8pj9C ![]() 9h1hC ![]() 9h1vC ![]() 9h21C ![]() 9h2gC ![]() 9h6tC ![]() 9h72C ![]() 9hp8C ![]() 9hp9C ![]() 9q85C 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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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_51812.map.gz / Format: CCP4 / Size: 30.5 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Unsharpened map | ||||||||||||||||||||||||||||||||||||
| 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:
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-Supplemental data
-Mask #1
| File | emd_51812_msk_1.map | ||||||||||||
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-Additional map: sharpened map (phenix.auto sharpen, 3.06A, b iso to d cut)
| File | emd_51812_additional_1.map | ||||||||||||
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| Annotation | sharpened map (phenix.auto_sharpen, 3.06A, b_iso_to_d_cut) | ||||||||||||
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| Density Histograms |
-Half map: half map 2
| File | emd_51812_half_map_1.map | ||||||||||||
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| Annotation | half map 2 | ||||||||||||
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| Density Histograms |
-Half map: half map 1
| File | emd_51812_half_map_2.map | ||||||||||||
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| Annotation | half map 1 | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Cas9:crRNA:tracrRNA bound to non-cognate duplex DNA
| Entire | Name: Cas9:crRNA:tracrRNA bound to non-cognate duplex DNA |
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| Components |
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-Supramolecule #1: Cas9:crRNA:tracrRNA bound to non-cognate duplex DNA
| Supramolecule | Name: Cas9:crRNA:tracrRNA bound to non-cognate duplex DNA / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#5 |
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| Source (natural) | Organism: Streptococcus thermophilus DGCC 7710 (bacteria) |
-Macromolecule #1: CRISPR-associated endonuclease Cas9
| Macromolecule | Name: CRISPR-associated endonuclease Cas9 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO / EC number: Hydrolases; Acting on ester bonds |
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| Source (natural) | Organism: Streptococcus thermophilus DGCC 7710 (bacteria) |
| Molecular weight | Theoretical: 162.498531 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MTKPYSIGLD IGTNSVGWAV ITDNYKVPSK KMKVLGNTSK KYIKKNLLGV LLFDSGITAE GRRLKRTARR RYTRRRNRIL YLQEIFSTE MATLDDAFFQ RLDDSFLVPD DKRDSKYPIF GNLVEEKVYH DEFPTIYHLR KYLADSTKKA DLRLVYLALA H MIKYRGHF ...String: MTKPYSIGLD IGTNSVGWAV ITDNYKVPSK KMKVLGNTSK KYIKKNLLGV LLFDSGITAE GRRLKRTARR RYTRRRNRIL YLQEIFSTE MATLDDAFFQ RLDDSFLVPD DKRDSKYPIF GNLVEEKVYH DEFPTIYHLR KYLADSTKKA DLRLVYLALA H MIKYRGHF LIEGEFNSKN NDIQKNFQDF LDTYNAIFES DLSLENSKQL EEIVKDKISK LEKKDRILKL FPGEKNSGIF SE FLKLIVG NQADFRKCFN LDEKASLHFS KESYDEDLET LLGYIGDDYS DVFLKAKKLY DAILLSGFLT VTDNETEAPL SSA MIKRYN EHKEDLALLK EYIRNISLKT YNEVFKDDTK NGYAGYIDGK TNQEDFYVYL KNLLAEFEGA DYFLEKIDRE DFLR KQRTF DNGSIPYQIH LQEMRAILDK QAKFYPFLAK NKERIEKILT FRIPYYVGPL ARGNSDFAWS IRKRNEKITP WNFED VIDK ESSAEAFINR MTSFDLYLPE EKVLPKHSLL YETFNVYNEL TKVRFIAESM RDYQFLDSKQ KKDIVRLYFK DKRKVT DKD IIEYLHAIYG YDGIELKGIE KQFNSSLSTY HDLLNIINDK EFLDDSSNEA IIEEIIHTLT IFEDREMIKQ RLSKFEN IF DKSVLKKLSR RHYTGWGKLS AKLINGIRDE KSGNTILDYL IDDGISNRNF MQLIHDDALS FKKKIQKAQI IGDEDKGN I KEVVKSLPGS PAIKKGILQS IKIVDELVKV MGGRKPESIV VEMARENQYT NQGKSNSQQR LKRLEKSLKE LGSKILKEN IPAKLSKIDN NALQNDRLYL YYLQNGKDMY TGDDLDIDRL SNYDIDHIIP QAFLKDNSID NKVLVSSASN RGKSDDFPSL EVVKKRKTF WYQLLKSKLI SQRKFDNLTK AERGGLLPED KAGFIQRQLV ETRQITKHVA RLLDEKFNNK KDENNRAVRT V KIITLKST LVSQFRKDFE LYKVREINDF HHAHDAYLNA VIASALLKKY PKLEPEFVYG DYPKYNSFRE RKSATEKVYF YS NIMNIFK KSISLADGRV IERPLIEVNE ETGESVWNKE SDLATVRRVL SYPQVNVVKK VEEQNHGLDR GKPKGLFNAN LSS KPKPNS NENLVGAKEY LDPKKYGGYA GISNSFAVLV KGTIEKGAKK KITNVLEFQG ISILDRINYR KDKLNFLLEK GYKD IELII ELPKYSLFEL SDGSRRMLAS ILSTNNKRGE IHKGNQIFLS QKFVKLLYHA KRISNTINEN HRKYVENHKK EFEEL FYYI LEFNENYVGA KKNGKLLNSA FQSWQNHSID ELCSSFIGPT GSERKGLFEL TSRGSAADFE FLGVKIPRYR DYTPSS LLK DATLIHQSVT GLYETRIDLA KLGEGLEGHH HHHH UniProtKB: CRISPR-associated endonuclease Cas9 |
-Macromolecule #2: crRNA (26-MER)
| Macromolecule | Name: crRNA (26-MER) / type: rna / ID: 2 / Number of copies: 1 |
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| Source (natural) | Organism: synthetic construct (others) |
| Molecular weight | Theoretical: 13.609083 KDa |
| Sequence | String: CGCUAAAGAG GAAGAGGACA GUUUUAGAGC UGUGUUGUUU CG |
-Macromolecule #3: tracrRNA (65-MER)
| Macromolecule | Name: tracrRNA (65-MER) / type: rna / ID: 3 / Number of copies: 1 |
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| Source (natural) | Organism: synthetic construct (others) |
| Molecular weight | Theoretical: 24.119357 KDa |
| Sequence | String: CGAAACAACA CAGCGAGUUA AAAUAAGGCU UAGUCCGUAC UCAACUUGAA AAGGUGGCAC CGAUUCGGUG UUUUU |
-Macromolecule #4: DNA (27-MER)
| Macromolecule | Name: DNA (27-MER) / type: dna / ID: 4 / Number of copies: 1 / Classification: DNA |
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| Source (natural) | Organism: synthetic construct (others) |
| Molecular weight | Theoretical: 15.003586 KDa |
| Sequence | String: (DG)(DA)(DT)(DG)(DT)(DC)(DT)(DT)(DC)(DC) (DA)(DA)(DT)(DT)(DT)(DA)(DC)(DT)(DA)(DC) (DT)(DC)(DG)(DT)(DT)(DC)(DT)(DG)(DG) (DT)(DG)(DT)(DT)(DT)(DC)(DT)(DC)(DG)(DA) (DG) (DG)(DC)(DG)(DT)(DC)(DA)(DG)(DC) (DC) |
-Macromolecule #5: DNA (27-MER)
| Macromolecule | Name: DNA (27-MER) / type: dna / ID: 5 / Number of copies: 1 / Classification: DNA |
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| Source (natural) | Organism: synthetic construct (others) |
| Molecular weight | Theoretical: 15.182787 KDa |
| Sequence | String: (DG)(DG)(DC)(DT)(DG)(DA)(DC)(DG)(DC)(DC) (DT)(DC)(DG)(DA)(DG)(DA)(DA)(DA)(DC)(DA) (DC)(DC)(DA)(DG)(DA)(DA)(DC)(DG)(DA) (DG)(DT)(DA)(DG)(DT)(DA)(DA)(DA)(DT)(DT) (DG) (DG)(DA)(DA)(DG)(DA)(DC)(DA)(DT) (DC) |
-Macromolecule #6: CALCIUM ION
| Macromolecule | Name: CALCIUM ION / type: ligand / ID: 6 / Number of copies: 1 / Formula: CA |
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| Molecular weight | Theoretical: 40.078 Da |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.5 |
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| Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON |
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 95 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS GLACIOS |
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| Software | Name: EPU (ver. 3.2) |
| Image recording | Film or detector model: FEI FALCON III (4k x 4k) / Detector mode: COUNTING / Number grids imaged: 1 / Number real images: 4083 / Average exposure time: 46.33 sec. / Average electron dose: 30.0 e/Å2 |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: OTHER / Imaging mode: OTHER / Cs: 2.7 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 92000 |
| Sample stage | Cooling holder cryogen: NITROGEN |
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Keywords
Streptococcus thermophilus DGCC 7710 (bacteria)
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Processing
FIELD EMISSION GUN
