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Open data
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Basic information
Entry | ![]() | |||||||||
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Title | Engineered OrufIscB-omegaRNA-target DNA complex | |||||||||
![]() | Engineered OrufIscB-omegaRNA-target DNA complex | |||||||||
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![]() | Gene editing / IscB / OMEGA / RNA-guided nuclease / RNA BINDING PROTEIN-RNA-DNA complex | |||||||||
Biological species | metagenome (others) / synthetic construct (others) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.71 Å | |||||||||
![]() | Xu P / Zhu S / Zhang F | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Evolution-guided protein design of IscB for persistent epigenome editing in vivo. Authors: Soumya Kannan / Han Altae-Tran / Shiyou Zhu / Peiyu Xu / Daniel Strebinger / Rachel Oshiro / Guilhem Faure / Lukas Moeller / Julie Pham / Kepler S Mears / Heyuan M Ni / Rhiannon K Macrae / Feng Zhang / ![]() Abstract: Naturally existing enzymes have been adapted for a variety of molecular technologies, with enhancements or modifications to the enzymes introduced to improve the desired function; however, it is ...Naturally existing enzymes have been adapted for a variety of molecular technologies, with enhancements or modifications to the enzymes introduced to improve the desired function; however, it is difficult to engineer variants with enhanced activity while maintaining specificity. Here we engineer the compact Obligate Mobile Element Guided Activity (OMEGA) RNA-guided endonuclease IscB and its guiding RNA (ωRNA) by combining ortholog screening, structure-guided protein domain design and RNA engineering, and deep learning-based structure prediction to generate an improved variant, NovaIscB. We show that the compact NovaIscB achieves up to 40% indel activity (~100-fold improvement over wild-type OgeuIscB) on the human genome with improved specificity relative to existing IscBs. We further show that NovaIscB can be fused with a methyltransferase to create a programmable transcriptional repressor, OMEGAoff, that is compact enough to be packaged in a single adeno-associated virus vector for persistent in vivo gene repression. This study highlights the power of combining natural diversity with protein engineering to design enhanced enzymes for molecular biology applications. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 89.5 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 21.9 KB 21.9 KB | Display Display | ![]() |
Images | ![]() | 65.1 KB | ||
Filedesc metadata | ![]() | 6.5 KB | ||
Others | ![]() ![]() ![]() ![]() | 51.6 MB 97.2 MB 95.6 MB 95.6 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 797.7 KB | Display | ![]() |
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Full document | ![]() | 797.2 KB | Display | |
Data in XML | ![]() | 13 KB | Display | |
Data in CIF | ![]() | 15.5 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
EMDB pages | ![]() ![]() |
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Map
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Annotation | Engineered OrufIscB-omegaRNA-target DNA complex | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.825 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Additional map: Additional Map 2
File | emd_49856_additional_1.map | ||||||||||||
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Annotation | Additional Map 2 | ||||||||||||
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Density Histograms |
-Additional map: Additional Map 1
File | emd_49856_additional_2.map | ||||||||||||
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Annotation | Additional Map 1 | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Half Map B
File | emd_49856_half_map_1.map | ||||||||||||
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Annotation | Half Map B | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Half Map A
File | emd_49856_half_map_2.map | ||||||||||||
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Annotation | Half Map A | ||||||||||||
Projections & Slices |
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Density Histograms |
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Sample components
-Entire : Engineered OrufIscB-omegaRNA-target DNA complex
Entire | Name: Engineered OrufIscB-omegaRNA-target DNA complex |
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Components |
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-Supramolecule #1: Engineered OrufIscB-omegaRNA-target DNA complex
Supramolecule | Name: Engineered OrufIscB-omegaRNA-target DNA complex / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4 |
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Source (natural) | Organism: metagenome (others) |
-Macromolecule #1: NTS
Macromolecule | Name: NTS / type: dna / ID: 1 / Number of copies: 1 / Classification: DNA |
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Source (natural) | Organism: synthetic construct (others) |
Molecular weight | Theoretical: 8.885773 KDa |
Sequence | String: (DA)(DA)(DA)(DA)(DT)(DG)(DA)(DC)(DT)(DT) (DC)(DT)(DC)(DA)(DT)(DA)(DA)(DA)(DA)(DT) (DT)(DC)(DC)(DC)(DG)(DG)(DG)(DT)(DA) |
-Macromolecule #3: DNA TS
Macromolecule | Name: DNA TS / type: dna / ID: 3 / Number of copies: 1 / Classification: DNA |
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Source (natural) | Organism: synthetic construct (others) |
Molecular weight | Theoretical: 12.030771 KDa |
Sequence | String: (DT)(DA)(DC)(DC)(DC)(DG)(DG)(DG)(DA)(DA) (DT)(DT)(DT)(DT)(DA)(DT)(DG)(DA)(DG)(DA) (DA)(DG)(DT)(DC)(DA)(DT)(DT)(DT)(DA) (DA)(DT)(DA)(DA)(DG)(DG)(DC)(DC)(DA)(DC) |
-Macromolecule #2: OrufIscB-REC-swap 49
Macromolecule | Name: OrufIscB-REC-swap 49 / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: metagenome (others) |
Molecular weight | Theoretical: 69.258656 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: RYVYVLDVDG KPLMPTCRFG KVRRMLKSGQ AKAVDTLPFT IQLTYKPRTR ILQPVTLGQD PGRTNIGMAA VRFDGKELGR FHCITRNKE IPKLMADRMA ARKASRRGER LARKRLARKL HTTAKHLNGR ILPGCSEPIA VKDIINTESR FNNRILTKCK V CGKNTPLR ...String: RYVYVLDVDG KPLMPTCRFG KVRRMLKSGQ AKAVDTLPFT IQLTYKPRTR ILQPVTLGQD PGRTNIGMAA VRFDGKELGR FHCITRNKE IPKLMADRMA ARKASRRGER LARKRLARKL HTTAKHLNGR ILPGCSEPIA VKDIINTESR FNNRILTKCK V CGKNTPLR RNVRELLLEN IVRFLPLESE LKETLKRTIL EGQQGNINKL FRKLRKVYKI TLNQKDWPGK NLTDIAKNKL PG RLPFCKE HFAENEKFTT IEKSTFRLTP TATQLLRTHI NLFRKLSGIL PVTDVAVELN KFAFMQLDNP EMKKREIDFC HGP LCGTGG LEAAVKEQQD GKCLLCGKES IGHYHHIVPR SRRGSNTIAN IAGLCPKCHE LVHKDADTAE SLTEMKTGLM KKYG GTSVL NQIIPKLVET LADLFPGHFH VTNGWNTKEF REKHHLEKDH DVDAYCIACS HLKPEETLVE TEPFEILQFR KHNRA IIHH QTERTYKLDG VTVAKNRKKR MEQKTDSLED WYVDMAKEHG KTQADAMRSR LTVIKSTRYY NTPGRMMPGT VFLYEG KRY VMTGQITNGK YYRAYGQEKR NFPAVKVRIL TKNTGLVFVA |
-Macromolecule #4: RNA (162-MER)
Macromolecule | Name: RNA (162-MER) / type: rna / ID: 4 / Number of copies: 1 |
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Source (natural) | Organism: metagenome (others) |
Molecular weight | Theoretical: 73.060102 KDa |
Sequence | String: GGGCCUUAUU AAAUGACUUC UCGUCAAUAA CCCAUGACUG AAGUCAUGGG CUUGCAGAUG CAGGUCCUGA UGGAAGAAAG GGUUACUGA GCAGAGCAGU GACAUGUCAU UCGCCGCGGG GUGAUUCCAA GCUCCGCGCU CCGGCUAGAC AUGCCCAUGC U UUGGAAAC ...String: GGGCCUUAUU AAAUGACUUC UCGUCAAUAA CCCAUGACUG AAGUCAUGGG CUUGCAGAUG CAGGUCCUGA UGGAAGAAAG GGUUACUGA GCAGAGCAGU GACAUGUCAU UCGCCGCGGG GUGAUUCCAA GCUCCGCGCU CCGGCUAGAC AUGCCCAUGC U UUGGAAAC UUUAACGGUA UGUGCGGUUU UCCGCUUAUA CCGGCUUACA ACAAAUAAGG AGUUAUUAG |
-Macromolecule #5: MAGNESIUM ION
Macromolecule | Name: MAGNESIUM ION / type: ligand / ID: 5 / Number of copies: 4 / Formula: MG |
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Molecular weight | Theoretical: 24.305 Da |
-Macromolecule #6: ZINC ION
Macromolecule | Name: ZINC ION / type: ligand / ID: 6 / Number of copies: 2 / Formula: ZN |
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Molecular weight | Theoretical: 65.409 Da |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 7.5 |
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Vitrification | Cryogen name: ETHANE-PROPANE |
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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: 48.82 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: OTHER / Imaging mode: OTHER / Nominal defocus max: 2.2 µm / Nominal defocus min: 0.8 µm |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |