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Yorodumi- PDB-8xtq: Comamonas testosteroni KF-1 circularly permuted group II intron 1... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 8xtq | |||||||||||||||||||||||||||||||||||||||
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| Title | Comamonas testosteroni KF-1 circularly permuted group II intron 1S state | |||||||||||||||||||||||||||||||||||||||
Components | RNA (808-MER) | |||||||||||||||||||||||||||||||||||||||
Keywords | RNA / CryoEM / Ribozyme | |||||||||||||||||||||||||||||||||||||||
| Function / homology | : / : / RNA / RNA (> 10) / RNA (> 100) Function and homology information | |||||||||||||||||||||||||||||||||||||||
| Biological species | Comamonas testosteroni KF-1 (bacteria) | |||||||||||||||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.96 Å | |||||||||||||||||||||||||||||||||||||||
Authors | Wang, L. / Xie, J.H. / Zhang, C. / Zou, J. / Huang, Z.R. / Shang, S.T. / Chen, X.Y. / Yang, Y. / Liu, J. / Dong, H.H. ...Wang, L. / Xie, J.H. / Zhang, C. / Zou, J. / Huang, Z.R. / Shang, S.T. / Chen, X.Y. / Yang, Y. / Liu, J. / Dong, H.H. / Huang, D.M. / Su, Z.M. | |||||||||||||||||||||||||||||||||||||||
| Funding support | China, 4items
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Citation | Journal: Nat Struct Mol Biol / Year: 2025Title: Structural basis of circularly permuted group II intron self-splicing. Authors: Liu Wang / Jiahao Xie / Chong Zhang / Jian Zou / Zirui Huang / Sitong Shang / Xingyu Chen / Yang Yang / Jianquan Liu / Haohao Dong / Dingming Huang / Zhaoming Su / ![]() Abstract: Circularly permuted group II introns (CP introns) consist of rearranged structural domains separated by two tethered exons, generating branched introns and circular exons via back-splicing. ...Circularly permuted group II introns (CP introns) consist of rearranged structural domains separated by two tethered exons, generating branched introns and circular exons via back-splicing. Structural and mechanistic understanding of circular RNA (circRNA) generation by CP introns remains elusive. We resolve cryo-electron microscopy structures of a natural CP intron in different states during back-splicing at a resolution of 2.5-2.9 Å. Domain 6 (D6) undergoes a conformational change of 65° after branching, to facilitate 3'-exon recognition and circularization. Previously unseen tertiary interactions compact the catalytic triad and D6 for splicing without protein, whereas a metal ion, M, is observed to stabilize the 5'-exon during splicing. While these unique features were not observed in canonical group II introns and spliceosomes, they are common in CP introns, as demonstrated by the cryo-EM structure of another CP intron discovered by comparative genomics analysis. Our results elucidate the mechanism of CP intron back-splicing dynamics, with potential applications in circRNA research and therapeutics. | |||||||||||||||||||||||||||||||||||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 8xtq.cif.gz | 412.8 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8xtq.ent.gz | 311.9 KB | Display | PDB format |
| PDBx/mmJSON format | 8xtq.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/xt/8xtq ftp://data.pdbj.org/pub/pdb/validation_reports/xt/8xtq | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 38647MC ![]() 8xtpC ![]() 8xtrC ![]() 8xtsC ![]() 9is7C M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: RNA chain | Mass: 262327.062 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Comamonas testosteroni KF-1 (bacteria) / Production host: synthetic construct (others) / References: GenBank: 2637094706 | ||||||
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| #2: Chemical | ChemComp-K / #3: Chemical | ChemComp-MG / Has ligand of interest | N | Has protein modification | N | |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: Comamonas testosteroni KF-1 circularly permuted group II intron 1S state Type: COMPLEX / Entity ID: #1 / Source: RECOMBINANT |
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| Source (natural) | Organism: Comamonas testosteroni KF-1 (bacteria) |
| Source (recombinant) | Organism: synthetic construct (others) |
| Buffer solution | pH: 7.5 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE |
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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: 1500 nm / Nominal defocus min: 800 nm |
| Image recording | Electron dose: 59 e/Å2 / Film or detector model: GATAN K2 QUANTUM (4k x 4k) |
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Processing
| EM software | Name: PHENIX / Category: model refinement |
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| CTF correction | Type: NONE |
| 3D reconstruction | Resolution: 2.96 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 46777 / Symmetry type: POINT |
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Comamonas testosteroni KF-1 (bacteria)
China, 4items
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