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- EMDB-16830: Structure of the mammalian Pol II-Elongin complex, lacking ELOA l... -

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Basic information

Entry
Database: EMDB / ID: EMD-16830
TitleStructure of the mammalian Pol II-Elongin complex, lacking ELOA latch (Focused map for elongin, map 5)
Map datamap 5(postprocess map). Focused map for Elongin in the composite map for the Pol II-Elongin (NoN) high resolution model
Sample
  • Complex: The Pol II-SPT6-Elongin transcription elongation complex
KeywordsTranscription elongation / Elongin / RNA polymerase II / TRANSCRIPTION
Biological speciesHomo sapiens (human)
Methodsingle particle reconstruction / cryo EM / Resolution: 3.61 Å
AuthorsChen Y / Kokic G / Dienemann C / Dybkov O / Urlaub H / Cramer P
Funding supportEuropean Union, Germany, 3 items
OrganizationGrant numberCountry
European Research Council (ERC)882357European Union
German Research Foundation (DFG)SFB860 Germany
German Research Foundation (DFG)EXC 2067/1-390729940 Germany
CitationJournal: Nat Struct Mol Biol / Year: 2023
Title: Structure of the transcribing RNA polymerase II-Elongin complex.
Authors: Ying Chen / Goran Kokic / Christian Dienemann / Olexandr Dybkov / Henning Urlaub / Patrick Cramer /
Abstract: Elongin is a heterotrimeric elongation factor for RNA polymerase (Pol) II transcription that is conserved among metazoa. Here, we report three cryo-EM structures of human Elongin bound to ...Elongin is a heterotrimeric elongation factor for RNA polymerase (Pol) II transcription that is conserved among metazoa. Here, we report three cryo-EM structures of human Elongin bound to transcribing Pol II. The structures show that Elongin subunit ELOA binds the RPB2 side of Pol II and anchors the ELOB-ELOC subunit heterodimer. ELOA contains a 'latch' that binds between the end of the Pol II bridge helix and funnel helices, thereby inducing a conformational change near the polymerase active center. The latch is required for the elongation-stimulatory activity of Elongin, but not for Pol II binding, indicating that Elongin functions by allosterically regulating the conformational mobility of the polymerase active center. Elongin binding to Pol II is incompatible with association of the super elongation complex, PAF1 complex and RTF1, which also contain an elongation-stimulatory latch element.
History
DepositionMar 12, 2023-
Header (metadata) releaseOct 18, 2023-
Map releaseOct 18, 2023-
UpdateDec 27, 2023-
Current statusDec 27, 2023Processing site: PDBe / Status: Released

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Structure visualization

Supplemental images

Downloads & links

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Map

FileDownload / File: emd_16830.map.gz / Format: CCP4 / Size: 325 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
Annotationmap 5(postprocess map). Focused map for Elongin in the composite map for the Pol II-Elongin (NoN) high resolution model
Voxel sizeX=Y=Z: 1.05 Å
Density
Contour LevelBy AUTHOR: 0.015
Minimum - Maximum-0.11892741 - 0.20936894
Average (Standard dev.)-0.00008420583 (±0.0016623221)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions440440440
Spacing440440440
CellA=B=C: 461.99997 Å
α=β=γ: 90.0 °

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Supplemental data

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Mask #1

Fileemd_16830_msk_1.map
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Half map: half map1 of map 5

Fileemd_16830_half_map_1.map
Annotationhalf map1 of map 5
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Half map: half map2 of map 5

Fileemd_16830_half_map_2.map
Annotationhalf map2 of map 5
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Sample components

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Entire : The Pol II-SPT6-Elongin transcription elongation complex

EntireName: The Pol II-SPT6-Elongin transcription elongation complex
Components
  • Complex: The Pol II-SPT6-Elongin transcription elongation complex

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Supramolecule #1: The Pol II-SPT6-Elongin transcription elongation complex

SupramoleculeName: The Pol II-SPT6-Elongin transcription elongation complex
type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#18
Details: The map is generated from a sub-class of a cryo-EM dataset for the Pol II-SPT6-Elongin complex.
Source (natural)Organism: Homo sapiens (human)

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Experimental details

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Structure determination

Methodcryo EM
Processingsingle particle reconstruction
Aggregation stateparticle

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Sample preparation

BufferpH: 7.5
GridModel: Quantifoil R3.5/1 / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Support film - topology: CONTINUOUS / Support film - Film thickness: 2.1
VitrificationCryogen name: ETHANE / Instrument: FEI VITROBOT MARK IV

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELDBright-field microscopy / Nominal defocus max: 7.5 µm / Nominal defocus min: 0.35000000000000003 µm
Image recordingFilm or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 40.09 e/Å2
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Startup modelType of model: NONE
Initial angle assignmentType: MAXIMUM LIKELIHOOD
Final angle assignmentType: MAXIMUM LIKELIHOOD
Final reconstructionResolution.type: BY AUTHOR / Resolution: 3.61 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 136189
FSC plot (resolution estimation)

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Atomic model buiding 1

RefinementSpace: REAL / Protocol: OTHER

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