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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | Ex vivo spore-silk A-ENA fibers | |||||||||
Map data | ||||||||||
Sample |
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Keywords | endospore / isopeptide bond / A-ENA / cross-linked / protein fiber / autocatalytic / PROTEIN FIBRIL | |||||||||
| Function / homology | : / Alpha-helical endospore appendage domain / Uncharacterized protein Function and homology information | |||||||||
| Biological species | ![]() | |||||||||
| Method | helical reconstruction / cryo EM / Resolution: 2.1 Å | |||||||||
Authors | Sleutel M / Sogues A / Remaut H | |||||||||
| Funding support | Belgium, 1 items
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Citation | Journal: Protein Sci / Year: 2018 Title: UCSF ChimeraX: Meeting modern challenges in visualization and analysis. Authors: Thomas D Goddard / Conrad C Huang / Elaine C Meng / Eric F Pettersen / Gregory S Couch / John H Morris / Thomas E Ferrin / ![]() Abstract: UCSF ChimeraX is next-generation software for the visualization and analysis of molecular structures, density maps, 3D microscopy, and associated data. It addresses challenges in the size, scope, and ...UCSF ChimeraX is next-generation software for the visualization and analysis of molecular structures, density maps, 3D microscopy, and associated data. It addresses challenges in the size, scope, and disparate types of data attendant with cutting-edge experimental methods, while providing advanced options for high-quality rendering (interactive ambient occlusion, reliable molecular surface calculations, etc.) and professional approaches to software design and distribution. This article highlights some specific advances in the areas of visualization and usability, performance, and extensibility. ChimeraX is free for noncommercial use and is available from http://www.rbvi.ucsf.edu/chimerax/ for Windows, Mac, and Linux. | |||||||||
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_52871.map.gz | 16.7 MB | EMDB map data format | |
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| Header (meta data) | emd-52871-v30.xml emd-52871.xml | 18.7 KB 18.7 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_52871_fsc.xml | 9.8 KB | Display | FSC data file |
| Images | emd_52871.png | 88.4 KB | ||
| Masks | emd_52871_msk_1.map | 103 MB | Mask map | |
| Filedesc metadata | emd-52871.cif.gz | 5.4 KB | ||
| Others | emd_52871_additional_1.map.gz emd_52871_half_map_1.map.gz emd_52871_half_map_2.map.gz | 17.1 MB 94.9 MB 94.9 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-52871 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-52871 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9ihhMC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_52871.map.gz / Format: CCP4 / Size: 103 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.766 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_52871_msk_1.map | ||||||||||||
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| Density Histograms |
-Additional map: #1
| File | emd_52871_additional_1.map | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_52871_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #2
| File | emd_52871_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Ex vivo spore-silk A-ENA fibers
| Entire | Name: Ex vivo spore-silk A-ENA fibers |
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| Components |
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-Supramolecule #1: Ex vivo spore-silk A-ENA fibers
| Supramolecule | Name: Ex vivo spore-silk A-ENA fibers / type: cell / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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| Source (natural) | Organism: ![]() |
-Macromolecule #1: Ex vivo spore-silk A-ENA fibers
| Macromolecule | Name: Ex vivo spore-silk A-ENA fibers / type: protein_or_peptide / ID: 1 / Number of copies: 29 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 10.91755 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MGMPTIPEGL DITRDQAINI ILASIGLEEL GLAHVINAEG EKVQAVVAGF EKETVTFDQL LATNESVTQT LKTVIKKEML LQFKLEEAK SLIQSSSPPS IS UniProtKB: Uncharacterized protein |
-Macromolecule #2: water
| Macromolecule | Name: water / type: ligand / ID: 2 / Number of copies: 599 / Formula: HOH |
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| Molecular weight | Theoretical: 18.015 Da |
| Chemical component information | ![]() ChemComp-HOH: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | helical reconstruction |
| Aggregation state | filament |
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Sample preparation
| Buffer | pH: 7 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | JEOL CRYO ARM 300 |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 60.0 e/Å2 |
| Electron beam | Acceleration voltage: 3000 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm |
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About Yorodumi




Keywords
Authors
Belgium, 1 items
Citation

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Processing
FIELD EMISSION GUN
