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Open data
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Basic information
| Entry | Database: PDB / ID: 6ff7 | ||||||
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| Title | human Bact spliceosome core structure | ||||||
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Keywords | SPLICING / spliceosome / human / HELA / BACT / dynamics | ||||||
| Function / homology | Function and homology informationpost-spliceosomal complex / RES complex / negative regulation of chemokine-mediated signaling pathway / snoRNA splicing / U11/U12 snRNP / regulation of retinoic acid receptor signaling pathway / post-mRNA release spliceosomal complex / 3'-5' RNA helicase activity / U2 snRNP binding / U7 snRNA binding ...post-spliceosomal complex / RES complex / negative regulation of chemokine-mediated signaling pathway / snoRNA splicing / U11/U12 snRNP / regulation of retinoic acid receptor signaling pathway / post-mRNA release spliceosomal complex / 3'-5' RNA helicase activity / U2 snRNP binding / U7 snRNA binding / histone pre-mRNA DCP binding / generation of catalytic spliceosome for first transesterification step / U7 snRNP / cis assembly of pre-catalytic spliceosome / histone pre-mRNA 3'end processing complex / regulation of vitamin D receptor signaling pathway / SLBP independent Processing of Histone Pre-mRNAs / SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs / spliceosome conformational change to release U4 (or U4atac) and U1 (or U11) / B-WICH complex / miRNA processing / nuclear retinoic acid receptor binding / embryonic brain development / oocyte development / protein methylation / alternative mRNA splicing, via spliceosome / U12-type spliceosomal complex / poly(A) binding / 7-methylguanosine cap hypermethylation / U1 snRNP binding / U2-type catalytic step 1 spliceosome / C2H2 zinc finger domain binding / RNA splicing, via transesterification reactions / methylosome / pICln-Sm protein complex / pre-mRNA binding / regulation of mRNA splicing, via spliceosome / positive regulation of mRNA splicing, via spliceosome / snRNP binding / mRNA 3'-end processing / blastocyst formation / sno(s)RNA-containing ribonucleoprotein complex / small nuclear ribonucleoprotein complex / splicing factor binding / Notch binding / host-mediated activation of viral transcription / SMN-Sm protein complex / spliceosomal tri-snRNP complex / mRNA cis splicing, via spliceosome / U2-type precatalytic spliceosome / P granule / positive regulation of vitamin D receptor signaling pathway / commitment complex / telomerase holoenzyme complex / nuclear vitamin D receptor binding / U2-type prespliceosome assembly / telomerase RNA binding / U2-type spliceosomal complex / Transport of Mature mRNA derived from an Intron-Containing Transcript / Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells / RUNX3 regulates NOTCH signaling / U2-type catalytic step 2 spliceosome / NOTCH4 Intracellular Domain Regulates Transcription / SAGA complex / U2 snRNP / RHOBTB1 GTPase cycle / U1 snRNP / RNA Polymerase II Transcription Termination / U4 snRNP / NOTCH3 Intracellular Domain Regulates Transcription / positive regulation of neurogenesis / U2-type prespliceosome / positive regulation of transcription by RNA polymerase III / inner cell mass cell proliferation / protein peptidyl-prolyl isomerization / K63-linked polyubiquitin modification-dependent protein binding / ubiquitin-ubiquitin ligase activity / nuclear androgen receptor binding / cyclosporin A binding / precatalytic spliceosome / generation of catalytic spliceosome for second transesterification step / WD40-repeat domain binding / Notch-HLH transcription pathway / lipid biosynthetic process / Formation of paraxial mesoderm / pattern recognition receptor activity / SMAD binding / positive regulation of transforming growth factor beta receptor signaling pathway / regulation of RNA splicing / spliceosomal complex assembly / mRNA 3'-splice site recognition / positive regulation of transcription by RNA polymerase I / mRNA Splicing - Minor Pathway / spliceosomal tri-snRNP complex assembly / Prp19 complex / U5 snRNA binding / U5 snRNP / intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator / protein K63-linked ubiquitination / blastocyst development Similarity search - Function | ||||||
| Biological species | Homo sapiens (human) | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 4.5 Å | ||||||
Authors | Haselbach, D. / Komarov, I. / Agafonov, D. / Hartmuth, K. / Graf, B. / Kastner, B. / Luehrmann, R. / Stark, H. | ||||||
Citation | Journal: Cell / Year: 2018Title: Structure and Conformational Dynamics of the Human Spliceosomal B Complex. Authors: David Haselbach / Ilya Komarov / Dmitry E Agafonov / Klaus Hartmuth / Benjamin Graf / Olexandr Dybkov / Henning Urlaub / Berthold Kastner / Reinhard Lührmann / Holger Stark / ![]() Abstract: The spliceosome is a highly dynamic macromolecular complex that precisely excises introns from pre-mRNA. Here we report the cryo-EM 3D structure of the human B spliceosome at 3.4 Å resolution. In ...The spliceosome is a highly dynamic macromolecular complex that precisely excises introns from pre-mRNA. Here we report the cryo-EM 3D structure of the human B spliceosome at 3.4 Å resolution. In the B state, the spliceosome is activated but not catalytically primed, so that it is functionally blocked prior to the first catalytic step of splicing. The spliceosomal core is similar to the yeast B spliceosome; important differences include the presence of the RNA helicase aquarius and peptidyl prolyl isomerases. To examine the overall dynamic behavior of the purified spliceosome, we developed a principal component analysis-based approach. Calculating the energy landscape revealed eight major conformational states, which we refined to higher resolution. Conformational differences of the highly flexible structural components between these eight states reveal how spliceosomal components contribute to the assembly of the spliceosome, allowing it to generate a dynamic interaction network required for its subsequent catalytic activation. | ||||||
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Structure visualization
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| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 6ff7.cif.gz | 2.8 MB | Display | PDBx/mmCIF format |
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| PDB format | pdb6ff7.ent.gz | 1.8 MB | Display | PDB format |
| PDBx/mmJSON format | 6ff7.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ff/6ff7 ftp://data.pdbj.org/pub/pdb/validation_reports/ff/6ff7 | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 4240MC ![]() 4233C ![]() 4234C ![]() 4235C ![]() 4236C ![]() 4237C ![]() 4238C ![]() 4239C ![]() 4247C ![]() 4248C ![]() 4249C ![]() 4250C ![]() 4251C ![]() 4252C ![]() 4253C ![]() 4254C ![]() 4255C ![]() 6ff4C M: map data used to model this data C: citing same article ( |
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| Similar structure data | |
| EM raw data | EMPIAR-10160 (Title: Conformational Dynamics of human Bact spliceosome / Data size: 2.8 TBData #1: aligned and summed micrograph stack of human Bact spliceosome [micrographs - single frame] Data #2: aligned, dose-weighted and summed micrograph stack of human Bact spliceosome [micrographs - single frame]) |
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Links
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Assembly
| Deposited unit | ![]()
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| 1 |
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Components
+Protein , 17 types, 18 molecules 13ABCDLOQRVty0Ufmq
+RNA chain , 4 types, 4 molecules 256Z
+Splicing factor 3A subunit ... , 3 types, 3 molecules 79p
+Splicing factor 3B subunit ... , 5 types, 6 molecules 8uvxzN
+Pre-mRNA-processing factor ... , 2 types, 5 molecules EGHIJ
+Pre-mRNA-splicing factor ... , 5 types, 5 molecules PKMTw
+Serine/arginine repetitive matrix protein ... , 2 types, 2 molecules SY
+Peptidyl-prolyl cis-trans isomerase ... , 2 types, 2 molecules so
+U5 small nuclear ribonucleoprotein ... , 2 types, 2 molecules Fr
+U2 small nuclear ribonucleoprotein ... , 2 types, 2 molecules WX
+Small nuclear ribonucleoprotein ... , 6 types, 12 molecules ahbicjdkelgn
+Non-polymers , 5 types, 20 molecules 








-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: human Bact spliceosome / Type: COMPLEX / Entity ID: #1-#50 / Source: NATURAL |
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| Molecular weight | Experimental value: NO |
| Source (natural) | Organism: Homo sapiens (human) |
| Buffer solution | pH: 7.6 |
| Specimen | Embedding applied: YES / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Specimen support | Grid material: COPPER / Grid mesh size: 200 divisions/in. / Grid type: Quantifoil R3.5/1 |
| EM embedding | Material: ice |
| 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: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: SPOT SCAN |
| Electron lens | Mode: BRIGHT FIELD |
| Image recording | Electron dose: 40 e/Å2 / Detector mode: INTEGRATING / Film or detector model: FEI FALCON III (4k x 4k) |
| Image scans | Sampling size: 14 µm / Width: 4096 / Height: 4096 |
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Processing
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| CTF correction | Type: PHASE FLIPPING ONLY | ||||||||||||||||
| Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||||||
| 3D reconstruction | Resolution: 4.5 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 165853 / Symmetry type: POINT |
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Homo sapiens (human)
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