[English] 日本語
Yorodumi- EMDB-2226: Single particle analysis of recombinant human anaphase promoting ... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-2226 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | Single particle analysis of recombinant human anaphase promoting complex (APC/C) | |||||||||
Map data | reconstruction of recombinant human APC/C | |||||||||
Sample |
| |||||||||
Keywords | Anaphase promoting complex / cyclosome / cell cycle / recombinant expression / single particle / 3-dimensional structure / ubiquitination | |||||||||
Biological species | Homo sapiens (human) | |||||||||
Method | single particle reconstruction / negative staining / Resolution: 20.0 Å | |||||||||
Authors | Zhang Z / Yang J / Kong EH / Chao WCH / Morris EP / da Fonseca PCA / Barford D | |||||||||
Citation | Journal: Biochem J / Year: 2013 Title: Recombinant expression, reconstitution and structure of human anaphase-promoting complex (APC/C). Authors: Ziguo Zhang / Jing Yang / Eric H Kong / William C H Chao / Edward P Morris / Paula C A da Fonseca / David Barford / Abstract: Mechanistic and structural studies of large multi-subunit assemblies are greatly facilitated by their reconstitution in heterologous recombinant systems. In the present paper, we describe the ...Mechanistic and structural studies of large multi-subunit assemblies are greatly facilitated by their reconstitution in heterologous recombinant systems. In the present paper, we describe the generation of recombinant human APC/C (anaphase-promoting complex/cyclosome), an E3 ubiquitin ligase that regulates cell-cycle progression. Human APC/C is composed of 14 distinct proteins that assemble into a complex of at least 19 subunits with a combined molecular mass of ~1.2 MDa. We show that recombinant human APC/C is correctly assembled, as judged by its capacity to ubiquitinate the budding yeast APC/C substrate Hsl1 (histone synthetic lethal 1) dependent on the APC/C co-activator Cdh1 [Cdc (cell division cycle) 20 homologue 1], and its three-dimensional reconstruction by electron microscopy and single-particle analysis. Successful reconstitution validates the subunit composition of human APC/C. The structure of human APC/C is compatible with the Saccharomyces cerevisiae APC/C homology model, and in contrast with endogenous human APC/C, no evidence for conformational flexibility of the TPR (tetratricopeptide repeat) lobe is observed. Additional density present in the human APC/C structure, proximal to Apc3/Cdc27 of the TPR lobe, is assigned to the TPR subunit Apc7, a subunit specific to vertebrate APC/C. | |||||||||
History |
|
-Structure visualization
Movie |
Movie viewer |
---|---|
Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_2226.map.gz | 10 MB | EMDB map data format | |
---|---|---|---|---|
Header (meta data) | emd-2226-v30.xml emd-2226.xml | 17.2 KB 17.2 KB | Display Display | EMDB header |
Images | emd_2226.tif | 137.6 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-2226 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-2226 | HTTPS FTP |
-Validation report
Summary document | emd_2226_validation.pdf.gz | 197.1 KB | Display | EMDB validaton report |
---|---|---|---|---|
Full document | emd_2226_full_validation.pdf.gz | 196.2 KB | Display | |
Data in XML | emd_2226_validation.xml.gz | 5.7 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-2226 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-2226 | HTTPS FTP |
-Related structure data
Similar structure data |
---|
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
---|
-Map
File | Download / File: emd_2226.map.gz / Format: CCP4 / Size: 10.2 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Annotation | reconstruction of recombinant human APC/C | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 3.4725 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
|
-Supplemental data
-Sample components
+Entire : recombinant human APC/C
+Supramolecule #1000: recombinant human APC/C
+Macromolecule #1: Apc1
+Macromolecule #2: Apc5
+Macromolecule #3: Apc15
+Macromolecule #4: Apc10
+Macromolecule #5: Apc8
+Macromolecule #6: Apc13
+Macromolecule #7: Apc2
+Macromolecule #8: Apc4
+Macromolecule #9: Apc11
+Macromolecule #10: Apc3
+Macromolecule #11: Apc16
+Macromolecule #12: Cdc26
+Macromolecule #13: Apc7
+Macromolecule #14: Apc6
-Experimental details
-Structure determination
Method | negative staining |
---|---|
Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 8 / Details: 20 mM HEPES NaOH pH 8.0, 200 mM NaCl, 2 mM DTT |
---|---|
Staining | Type: NEGATIVE / Details: grids stained with 2% (w/v) uranyl acetate |
Grid | Details: Quantifoil R1.2/1.3 grids coated with a thin layer of carbon |
Vitrification | Cryogen name: NONE / Instrument: OTHER |
-Electron microscopy
Microscope | FEI TECNAI F20 |
---|---|
Date | Jan 1, 2012 |
Image recording | Category: CCD / Film or detector model: TVIPS TEMCAM-F415 (4k x 4k) / Average electron dose: 100 e/Å2 Details: on recording each adjacent boxes of 2x2 pixels were averaged |
Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus min: 1.2 µm / Nominal magnification: 50000 |
Sample stage | Specimen holder model: SIDE ENTRY, EUCENTRIC |
Experimental equipment | Model: Tecnai F20 / Image courtesy: FEI Company |
-Image processing
Details | Particles were manually selected using the EMAN boxer software. The images were analysed using a combination of IMAGIC and Spider software. |
---|---|
Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 20.0 Å / Resolution method: OTHER / Software - Name: Spider, Imagic / Number images used: 5639 |