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Yorodumi- EMDB-17897: Chaetomium thermophilum pre-60S State 3 - post-5S rotation with R... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-17897 | |||||||||
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Title | Chaetomium thermophilum pre-60S State 3 - post-5S rotation with Rix1 complex with Foot - local refinement - uL1-Nop53N | |||||||||
Map data | Chaetomium thermophilum pre-60S State 3 - post-5S rotation with Rix1 complex with Foot - local refinement - uL1-Nop53N - local resolution filtered | |||||||||
Sample |
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Keywords | biogenesis / pre-60S / 5S RNP / RIBOSOME | |||||||||
Biological species | Thermochaetoides thermophila DSM 1495 (fungus) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.91 Å | |||||||||
Authors | Thoms M / Cheng J / Denk T / Berninghausen O / Beckmann R | |||||||||
Funding support | European Union, 1 items
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Citation | Journal: EMBO Rep / Year: 2023 Title: Structural insights into coordinating 5S RNP rotation with ITS2 pre-RNA processing during ribosome formation. Authors: Matthias Thoms / Benjamin Lau / Jingdong Cheng / Lisa Fromm / Timo Denk / Nikola Kellner / Dirk Flemming / Paulina Fischer / Laurent Falquet / Otto Berninghausen / Roland Beckmann / Ed Hurt / Abstract: The rixosome defined in Schizosaccharomyces pombe and humans performs diverse roles in pre-ribosomal RNA processing and gene silencing. Here, we isolate and describe the conserved rixosome from ...The rixosome defined in Schizosaccharomyces pombe and humans performs diverse roles in pre-ribosomal RNA processing and gene silencing. Here, we isolate and describe the conserved rixosome from Chaetomium thermophilum, which consists of two sub-modules, the sphere-like Rix1-Ipi3-Ipi1 and the butterfly-like Las1-Grc3 complex, connected by a flexible linker. The Rix1 complex of the rixosome utilizes Sda1 as landing platform on nucleoplasmic pre-60S particles to wedge between the 5S rRNA tip and L1-stalk, thereby facilitating the 180° rotation of the immature 5S RNP towards its mature conformation. Upon rixosome positioning, the other sub-module with Las1 endonuclease and Grc3 polynucleotide-kinase can reach a strategic position at the pre-60S foot to cleave and 5' phosphorylate the nearby ITS2 pre-rRNA. Finally, inward movement of the L1 stalk permits the flexible Nop53 N-terminus with its AIM motif to become positioned at the base of the L1-stalk to facilitate Mtr4 helicase-exosome participation for completing ITS2 removal. Thus, the rixosome structure elucidates the coordination of two central ribosome biogenesis events, but its role in gene silencing may adapt similar strategies. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_17897.map.gz | 2.6 MB | EMDB map data format | |
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Header (meta data) | emd-17897-v30.xml emd-17897.xml | 23.2 KB 23.2 KB | Display Display | EMDB header |
Images | emd_17897.png | 121.7 KB | ||
Filedesc metadata | emd-17897.cif.gz | 4.1 KB | ||
Others | emd_17897_additional_1.map.gz emd_17897_half_map_1.map.gz emd_17897_half_map_2.map.gz | 239.6 MB 442 MB 442 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-17897 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-17897 | HTTPS FTP |
-Validation report
Summary document | emd_17897_validation.pdf.gz | 901.2 KB | Display | EMDB validaton report |
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Full document | emd_17897_full_validation.pdf.gz | 900.7 KB | Display | |
Data in XML | emd_17897_validation.xml.gz | 18.4 KB | Display | |
Data in CIF | emd_17897_validation.cif.gz | 22.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-17897 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-17897 | HTTPS FTP |
-Related structure data
Related structure data | 8ptwC 8puwC 8pv1C 8pv2C 8pv3C 8pv4C 8pv5C 8pv6C 8pv7C 8pv8C 8pvkC 8pvlC C: citing same article (ref.) |
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-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_17897.map.gz / Format: CCP4 / Size: 476.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | Chaetomium thermophilum pre-60S State 3 - post-5S rotation with Rix1 complex with Foot - local refinement - uL1-Nop53N - local resolution filtered | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.045 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Additional map: Chaetomium thermophilum pre-60S State 3 - post-5S rotation...
File | emd_17897_additional_1.map | ||||||||||||
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Annotation | Chaetomium thermophilum pre-60S State 3 - post-5S rotation with Rix1 complex with Foot - local refinement - uL1-Nop53N | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Chaetomium thermophilum pre-60S State 3 - post-5S rotation...
File | emd_17897_half_map_1.map | ||||||||||||
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Annotation | Chaetomium thermophilum pre-60S State 3 - post-5S rotation with Rix1 complex with Foot - local refinement - uL1-Nop53N - half map A | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Chaetomium thermophilum pre-60S State 3 - post-5S rotation...
File | emd_17897_half_map_2.map | ||||||||||||
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Annotation | Chaetomium thermophilum pre-60S State 3 - post-5S rotation with Rix1 complex with Foot - local refinement - uL1-Nop53N - half map B | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Chaetomium thermophilum pre-60S State 3 - post-5S rotation with R...
Entire | Name: Chaetomium thermophilum pre-60S State 3 - post-5S rotation with Rix1 complex with Foot - local refinement - uL1-Nop53N |
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Components |
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-Supramolecule #1: Chaetomium thermophilum pre-60S State 3 - post-5S rotation with R...
Supramolecule | Name: Chaetomium thermophilum pre-60S State 3 - post-5S rotation with Rix1 complex with Foot - local refinement - uL1-Nop53N type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#62 |
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Source (natural) | Organism: Thermochaetoides thermophila DSM 1495 (fungus) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.5 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Average electron dose: 46.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.5 µm / Nominal defocus min: 0.4 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: NONE |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 2.91 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 26753 |
Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |