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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-1847 | |||||||||
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| Title | Human 35S U5 snRNP | |||||||||
Map data | This is a 3D map of the human 35S U5 snRNP | |||||||||
Sample |
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Keywords | Spliceosome / pre-mRNA splicing / 35S U5 snRNP | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 27.8 Å | |||||||||
Authors | Golas MM / Sander B / Bessonov S / Grote M / Wolf E / Kastner B / Stark H / Luhrmann R | |||||||||
Citation | Journal: Mol Cell / Year: 2010Title: 3D cryo-EM structure of an active step I spliceosome and localization of its catalytic core. Authors: Monika M Golas / Bjoern Sander / Sergey Bessonov / Michael Grote / Elmar Wolf / Berthold Kastner / Holger Stark / Reinhard Lührmann / ![]() Abstract: The spliceosome excises introns from pre-mRNA in a two-step splicing reaction. So far, the three-dimensional (3D) structure of a spliceosome with preserved catalytic activity has remained elusive. ...The spliceosome excises introns from pre-mRNA in a two-step splicing reaction. So far, the three-dimensional (3D) structure of a spliceosome with preserved catalytic activity has remained elusive. Here, we determined the 3D structure of the human, catalytically active step I spliceosome (C complex) by cryo-electron microscopy (cryo-EM) in vitrified ice. Via immunolabeling we mapped the position of the 5' exon. The C complex contains an unusually salt-stable ribonucleoprotein (RNP) core that harbors its catalytic center. We determined the 3D structure of this RNP core and also that of a post-step II particle, the 35S U5 snRNP, which contains most of the C complex core proteins. As C complex domains could be recognized in these structures, their position in the C complex could be determined, thereby allowing the region harboring the spliceosome's catalytic core to be localized. | |||||||||
| History |
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Structure visualization
| Movie |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_1847.map.gz | 2 MB | EMDB map data format | |
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| Header (meta data) | emd-1847-v30.xml emd-1847.xml | 6.4 KB 6.4 KB | Display Display | EMDB header |
| Images | emd_1847.png | 67.7 KB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-1847 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-1847 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_1847.map.gz / Format: CCP4 / Size: 7.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | This is a 3D map of the human 35S U5 snRNP | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 5.1 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : Human spliceosomal 35S U5 snRNP
| Entire | Name: Human spliceosomal 35S U5 snRNP |
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| Components |
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-Supramolecule #1000: Human spliceosomal 35S U5 snRNP
| Supramolecule | Name: Human spliceosomal 35S U5 snRNP / type: sample / ID: 1000 / Number unique components: 1 |
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| Molecular weight | Theoretical: 2.4 MDa |
-Supramolecule #1: Human spliceosomal 35S U5 snRNP
| Supramolecule | Name: Human spliceosomal 35S U5 snRNP / type: organelle_or_cellular_component / ID: 1 / Name.synonym: 35S U5 snRNP / Recombinant expression: No |
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| Source (natural) | Organism: Homo sapiens (human) / synonym: Human |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Vitrification | Cryogen name: ETHANE / Instrument: OTHER |
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Electron microscopy
| Microscope | FEI/PHILIPS CM200FEG |
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| Electron beam | Acceleration voltage: 160 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD |
| Sample stage | Specimen holder: Eucentric / Specimen holder model: GATAN LIQUID NITROGEN |
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Image processing
| Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 27.8 Å / Resolution method: FSC 0.5 CUT-OFF |
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Keywords
Homo sapiens (human)
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