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Yorodumi- EMDB-6684: Cryo-EM structure of the Catalytic Step II spliceosome (C* comple... -
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Basic information
| Entry | Database: EMDB / ID: EMD-6684 | |||||||||
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| Title | Cryo-EM structure of the Catalytic Step II spliceosome (C* complex) at 4.0 angstrom resolution | |||||||||
Map data | Yeast Step II Catalytically Activated Spliceosome, C* spliceosome | |||||||||
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| Function / homology | Function and homology informationRNA exon ligation / snRNA metabolic process / snRNA modification / U2-type post-spliceosomal complex / mRNA branch site recognition / U2-type post-mRNA release spliceosomal complex / cellular bud site selection / generation of catalytic spliceosome for first transesterification step / 3'-5' RNA helicase activity / nuclear mRNA surveillance ...RNA exon ligation / snRNA metabolic process / snRNA modification / U2-type post-spliceosomal complex / mRNA branch site recognition / U2-type post-mRNA release spliceosomal complex / cellular bud site selection / generation of catalytic spliceosome for first transesterification step / 3'-5' RNA helicase activity / nuclear mRNA surveillance / cis assembly of pre-catalytic spliceosome / 7-methylguanosine cap hypermethylation / pICln-Sm protein complex / snRNP binding / ATP-dependent activity, acting on RNA / small nuclear ribonucleoprotein complex / splicing factor binding / SMN-Sm protein complex / post-mRNA release spliceosomal complex / spliceosomal tri-snRNP complex / commitment complex / U2-type spliceosomal complex / U2-type prespliceosome assembly / pre-mRNA binding / U4/U6 snRNP / U2-type catalytic step 2 spliceosome / spliceosome conformational change to release U4 (or U4atac) and U1 (or U11) / U1 snRNP / U2 snRNP / U2-type catalytic step 1 spliceosome / U4 snRNP / U2-type prespliceosome / mRNA cis splicing, via spliceosome / generation of catalytic spliceosome for second transesterification step / poly(U) RNA binding / precatalytic spliceosome / mRNA 5'-splice site recognition / mRNA 3'-splice site recognition / spliceosomal complex assembly / pre-mRNA intronic binding / Gap-filling DNA repair synthesis and ligation in TC-NER / Prp19 complex / U2 snRNA binding / U5 snRNA binding / spliceosomal tri-snRNP complex assembly / DNA replication origin binding / U5 snRNP / Dual incision in TC-NER / U1 snRNA binding / U6 snRNA binding / DNA replication initiation / U4/U6 x U5 tri-snRNP complex / protein K63-linked ubiquitination / spliceosomal snRNP assembly / catalytic step 2 spliceosome / positive regulation of cell cycle / spliceosomal complex / nuclear periphery / positive regulation of RNA splicing / mRNA splicing, via spliceosome / RING-type E3 ubiquitin transferase / metallopeptidase activity / ubiquitin-protein transferase activity / ubiquitin protein ligase activity / RNA helicase / mRNA binding / chromatin binding / GTPase activity / GTP binding / chromatin / ATP hydrolysis activity / mitochondrion / RNA binding / metal ion binding / ATP binding / identical protein binding / nucleus / cytosol / cytoplasm Similarity search - Function | |||||||||
| Biological species | ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 4.0 Å | |||||||||
Authors | Yan C / Wan R / Bai R / Huang G / Shi Y | |||||||||
Citation | Journal: Science / Year: 2017Title: Structure of a yeast step II catalytically activated spliceosome. Authors: Chuangye Yan / Ruixue Wan / Rui Bai / Gaoxingyu Huang / Yigong Shi / ![]() Abstract: Each cycle of precursor messenger RNA (pre-mRNA) splicing comprises two sequential reactions, first freeing the 5' exon and generating an intron lariat-3' exon and then ligating the two exons and ...Each cycle of precursor messenger RNA (pre-mRNA) splicing comprises two sequential reactions, first freeing the 5' exon and generating an intron lariat-3' exon and then ligating the two exons and releasing the intron lariat. The second reaction is executed by the step II catalytically activated spliceosome (known as the C* complex). Here, we present the cryo-electron microscopy structure of a C* complex from Saccharomyces cerevisiae at an average resolution of 4.0 angstroms. Compared with the preceding spliceosomal complex (C complex), the lariat junction has been translocated by 15 to 20 angstroms to vacate space for the incoming 3'-exon sequences. The step I splicing factors Cwc25 and Yju2 have been dissociated from the active site. Two catalytic motifs from Prp8 (the 1585 loop and the β finger of the ribonuclease H-like domain), along with the step II splicing factors Prp17 and Prp18 and other surrounding proteins, are poised to assist the second transesterification. These structural features, together with those reported for other spliceosomal complexes, yield a near-complete mechanistic picture on the splicing cycle. | |||||||||
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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_6684.map.gz | 228.9 MB | EMDB map data format | |
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| Header (meta data) | emd-6684-v30.xml emd-6684.xml | 8.4 KB 8.4 KB | Display Display | EMDB header |
| Images | emd_6684.png | 195.9 KB | ||
| Archive directory | https://data.pdbj.org/pub/emdb/structures/EMD-6684 ftp://data.pdbj.org/pub/emdb/structures/EMD-6684 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 5wsgMC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data |
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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_6684.map.gz / Format: CCP4 / Size: 244.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Yeast Step II Catalytically Activated Spliceosome, C* spliceosome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.306 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 : C* spliceosome
| Entire | Name: C* spliceosome |
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| Components |
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-Supramolecule #1: C* spliceosome
| Supramolecule | Name: C* spliceosome / type: complex / ID: 1 / Parent: 0 |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 1.5 MDa |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 0.27 mg/mL |
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| Buffer | pH: 8 |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Average electron dose: 1.6 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm |
| Sample stage | Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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