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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | FnCas9 perfect match DNA product state | |||||||||
Map data | FnCas9 perfect match DNA product state | |||||||||
Sample |
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Keywords | Francisella novicida-Cas9 / CRISPR / Cas9 / IMMUNE SYSTEM / Hydrolase-DNA-RNA complex | |||||||||
| Function / homology | Function and homology informationendonuclease activity / defense response to virus / Hydrolases; Acting on ester bonds / DNA binding / RNA binding / metal ion binding Similarity search - Function | |||||||||
| Biological species | Francisella tularensis subsp. novicida (bacteria) / Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.6 Å | |||||||||
Authors | Hibshman GN / Taylor DW | |||||||||
| Funding support | United States, 2 items
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Citation | Journal: Nucleic Acids Res / Year: 2025Title: Structural basis of a dual-function type II-B CRISPR-Cas9. Authors: Grace N Hibshman / David W Taylor / ![]() Abstract: Cas9 from Streptococcus pyogenes (SpCas9) revolutionized genome editing by enabling programmable DNA cleavage guided by an RNA. However, SpCas9 tolerates mismatches in the DNA-RNA duplex, which can ...Cas9 from Streptococcus pyogenes (SpCas9) revolutionized genome editing by enabling programmable DNA cleavage guided by an RNA. However, SpCas9 tolerates mismatches in the DNA-RNA duplex, which can lead to deleterious off-target editing. Here, we reveal that Cas9 from Francisella novicida (FnCas9) possesses a unique structural feature-the REC3 clamp-that underlies its intrinsic high-fidelity DNA targeting. Through kinetic and structural analyses, we show that the REC3 clamp forms critical contacts with the PAM-distal region of the R-loop, thereby imposing a novel checkpoint during enzyme activation. Notably, F. novicida encodes a noncanonical small CRISPR-associated RNA (scaRNA) that enables FnCas9 to repress an endogenous bacterial lipoprotein gene, subverting host immune detection. Structures of FnCas9 with scaRNA illustrate how partial R-loop complementarity hinders REC3 clamp docking and prevents cleavage in favor of transcriptional repression. The REC3 clamp is conserved across type II-B CRISPR-Cas9 systems, pointing to a potential path for engineering precise genome editors or developing novel antibacterial strategies. These findings reveal the molecular basis of heightened specificity and virulence enabled by FnCas9, with broad implications for biotechnology and therapeutic development. | |||||||||
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_48052.map.gz | 257.4 MB | EMDB map data format | |
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| Header (meta data) | emd-48052-v30.xml emd-48052.xml | 19.8 KB 19.8 KB | Display Display | EMDB header |
| Images | emd_48052.png | 133 KB | ||
| Filedesc metadata | emd-48052.cif.gz | 7.2 KB | ||
| Others | emd_48052_half_map_1.map.gz emd_48052_half_map_2.map.gz | 475.8 MB 475.8 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-48052 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-48052 | HTTPS FTP |
-Validation report
| Summary document | emd_48052_validation.pdf.gz | 859.6 KB | Display | EMDB validaton report |
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| Full document | emd_48052_full_validation.pdf.gz | 859.2 KB | Display | |
| Data in XML | emd_48052_validation.xml.gz | 19 KB | Display | |
| Data in CIF | emd_48052_validation.cif.gz | 22.8 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-48052 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-48052 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9ehfMC ![]() 9ehgC ![]() 9ehhC ![]() 9ehrC ![]() 9ehwC ![]() 9ehxC ![]() 9n6tC 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_48052.map.gz / Format: CCP4 / Size: 512 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | FnCas9 perfect match DNA product state | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.8332 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: Half Map A
| File | emd_48052_half_map_1.map | ||||||||||||
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| Annotation | Half Map A | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: Half Map B
| File | emd_48052_half_map_2.map | ||||||||||||
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| Annotation | Half Map B | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : Ternary complex of FnCas with HBB gRNA and HBB DNA
| Entire | Name: Ternary complex of FnCas with HBB gRNA and HBB DNA |
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| Components |
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-Supramolecule #1: Ternary complex of FnCas with HBB gRNA and HBB DNA
| Supramolecule | Name: Ternary complex of FnCas with HBB gRNA and HBB DNA / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#5 |
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| Source (natural) | Organism: Francisella tularensis subsp. novicida (bacteria) |
| Molecular weight | Theoretical: 190.329 KDa |
-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: Francisella tularensis subsp. novicida (bacteria) |
| Molecular weight | Theoretical: 190.756188 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MNFKILPIAI DLGVKNTGVF SAFYQKGTSL ERLDNKNGKV YELSKDSYTL LMNNRTARRH QRRGIDRKQL VKRLFKLIWT EQLNLEWDK DTQQAISFLF NRRGFSFITD GYSPEYLNIV PEQVKAILMD IFDDYNGEDD LDSYLKLATE QESKISEIYN K LMQKILEF ...String: MNFKILPIAI DLGVKNTGVF SAFYQKGTSL ERLDNKNGKV YELSKDSYTL LMNNRTARRH QRRGIDRKQL VKRLFKLIWT EQLNLEWDK DTQQAISFLF NRRGFSFITD GYSPEYLNIV PEQVKAILMD IFDDYNGEDD LDSYLKLATE QESKISEIYN K LMQKILEF KLMKLCTDIK DDKVSTKTLK EITSYEFELL ADYLANYSES LKTQKFSYTD KQGNLKELSY YHHDKYNIQE FL KRHATIN DRILDTLLTD DLDIWNFNFE KFDFDKNEEK LQNQEDKDHI QAHLHHFVFA VNKIKSEMAS GGRHRSQYFQ EIT NVLDEN NHQEGYLKNF CENLHNKKYS NLSVKNLVNL IGNLSNLELK PLRKYFNDKI HAKADHWDEQ KFTETYCHWI LGEW RVGVK DQDKKDGAKY SYKDLCNELK QKVTKAGLVD FLLELDPCRT IPPYLDNNNR KPPKCQSLIL NPKFLDNQYP NWQQY LQEL KKLQSIQNYL DSFETDLKVL KSSKDQPYFV EYKSSNQQIA SGQRDYKDLD ARILQFIFDR VKASDELLLN EIYFQA KKL KQKASSELEK LESSKKLDEV IANSQLSQIL KSQHTNGIFE QGTFLHLVCK YYKQRQRARD SRLYIMPEYR YDKKLHK YN NTGRFDDDNQ LLTYCNHKPR QKRYQLLNDL AGVLQVSPNF LKDKIGSDDD LFISKWLVEH IRGFKKACED SLKIQKDN R GLLNHKINIA RNTKGKCEKE IFNLICKIEG SEDKKGNYKH GLAYELGVLL FGEPNEASKP EFDRKIKKFN SIYSFAQIQ QIAFAERKGN ANTCAVCSAD NAHRMQQIKI TEPVEDNKDK IILSAKAQRL PAIPTRIVDG AVKKMATILA KNIVDDNWQN IKQVLSAKH QLHIPIITES NAFEFEPALA DVKGKSLKDR RKKALERISP ENIFKDKNNR IKEFAKGISA YSGANLTDGD F DGAKEELD HIIPRSHKKY GTLNDEANLI CVTRGDNKNK GNRIFCLRDL ADNYKLKQFE TTDDLEIEKK IADTIWDANK KD FKFGNYR SFINLTPQEQ KAFRHALFLA DENPIKQAVI RAINNRNRTF VNGTQRYFAE VLANNIYLRA KKENLNTDKI SFD YFGIPT IGNGRGIAEI RQLYEKVDSD IQAYAKGDKP QASYSHLIDA MLAFCIAADE HRNDGSIGLE IDKNYSLYPL DKNT GEVFT KDIFSQIKIT DNEFSDKKLV RKKAIEGFNT HRQMTRDGIY AENYLPILIH KELNEVRKGY TWKNSEEIKI FKGKK YDIQ QLNNLVYCLK FVDKPISIDI QISTLEELRN ILTTNNIAAT AEYYYINLKT QKLHEYYIEN YNTALGYKKY SKEMEF LRS LAYRSERVKI KSIDDVKQVL DKDSNFIIGK ITLPFKKEWQ RLYREWQNTT IKDDYEFLKS FFNVKSITKL HKKVRKD FS LPISTNEGKF LVKRKTWDNN FIYQILNDSD SRADGTKPFI PAFDISKNEI VEAIIDSFTS KNIFWLPKNI ELQKVDNK N IFAIDTSKWF EVETPSDLRD IGIATIQYKI DNNSRPKVRV KLDYVIDDDS KINYFMNHSL LKSRYPDKVL EILKQSTII EFESSGFNKT IKEMLGMKLA GIYNETSNN UniProtKB: CRISPR-associated endonuclease Cas9 |
-Macromolecule #2: gRNA
| Macromolecule | Name: gRNA / type: rna / ID: 2 / Number of copies: 1 |
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| Source (natural) | Organism: Francisella tularensis subsp. novicida (bacteria) |
| Molecular weight | Theoretical: 30.039703 KDa |
| Sequence | String: AGUAACGGCA GACUUCUCCU CGUUUCAGUU GCGCCGAAAG GCGCUCUGUA AUCAUUUAAA AGUAUUUUGA ACGGACCUCU GUUUGACAC GUCUG |
-Macromolecule #3: HBB DNA TS 1
| Macromolecule | Name: HBB DNA TS 1 / type: dna / ID: 3 / Number of copies: 1 / Classification: DNA |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 3.647393 KDa |
| Sequence | String: (DC)(DC)(DG)(DA)(DT)(DA)(DC)(DC)(DT)(DG) (DA)(DG) |
-Macromolecule #4: HBB DNA NTS
| Macromolecule | Name: HBB DNA NTS / type: dna / ID: 4 / Number of copies: 1 / Classification: DNA |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 2.795847 KDa |
| Sequence | String: (DA)(DG)(DG)(DT)(DA)(DT)(DC)(DG)(DG) |
-Macromolecule #5: HBB DNA TS 2
| Macromolecule | Name: HBB DNA TS 2 / type: dna / ID: 5 / Number of copies: 1 / Classification: DNA |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 5.53159 KDa |
| Sequence | String: (DG)(DA)(DG)(DA)(DA)(DG)(DT)(DC)(DT)(DG) (DC)(DC)(DG)(DT)(DT)(DA)(DC)(DT) |
-Macromolecule #6: MAGNESIUM ION
| Macromolecule | Name: MAGNESIUM ION / type: ligand / ID: 6 / Number of copies: 2 / Formula: MG |
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| Molecular weight | Theoretical: 24.305 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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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 80.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.5 µm / Nominal defocus min: 1.5 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Keywords
Francisella tularensis subsp. novicida (bacteria)
Homo sapiens (human)
Authors
United States, 2 items
Citation













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Processing
FIELD EMISSION GUN
