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Yorodumi- EMDB-12859: Model of closed pentamer of the Haliangium ochraceum encapsulin f... -
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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-12859 | |||||||||
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| Title | Model of closed pentamer of the Haliangium ochraceum encapsulin from symmetry expansion of icosahedral single particle reconstruction | |||||||||
Map data | Refine 3D map | |||||||||
Sample |
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Keywords | Encapsulin / encapsulated ferritin / haliangium ochraceum / VIRUS LIKE PARTICLE | |||||||||
| Function / homology | Function and homology informationencapsulin nanocompartment / ferroxidase / ferroxidase activity / iron ion transport / intracellular iron ion homeostasis / metal ion binding Similarity search - Function | |||||||||
| Biological species | Haliangium ochraceum (bacteria) / Haliangium ochraceum (strain DSM 14365 / JCM 11303 / SMP-2) (bacteria) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.4 Å | |||||||||
Authors | Marles-Wright J / Basle A | |||||||||
| Funding support | United Kingdom, 1 items
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Citation | Journal: Sci Adv / Year: 2022Title: Pore dynamics and asymmetric cargo loading in an encapsulin nanocompartment. Authors: Jennifer Ross / Zak McIver / Thomas Lambert / Cecilia Piergentili / Jasmine Emma Bird / Kelly J Gallagher / Faye L Cruickshank / Patrick James / Efrain Zarazúa-Arvizu / Louise E Horsfall / ...Authors: Jennifer Ross / Zak McIver / Thomas Lambert / Cecilia Piergentili / Jasmine Emma Bird / Kelly J Gallagher / Faye L Cruickshank / Patrick James / Efrain Zarazúa-Arvizu / Louise E Horsfall / Kevin J Waldron / Marcus D Wilson / C Logan Mackay / Arnaud Baslé / David J Clarke / Jon Marles-Wright / ![]() Abstract: Encapsulins are protein nanocompartments that house various cargo enzymes, including a family of decameric ferritin-like proteins. Here, we study a recombinant encapsulin:encapsulated ferritin ...Encapsulins are protein nanocompartments that house various cargo enzymes, including a family of decameric ferritin-like proteins. Here, we study a recombinant encapsulin:encapsulated ferritin complex using cryo-electron microscopy and hydrogen/deuterium exchange mass spectrometry to gain insight into the structural relationship between the encapsulin shell and its protein cargo. An asymmetric single-particle reconstruction reveals four encapsulated ferritin decamers in a tetrahedral arrangement within the encapsulin nanocompartment. This leads to a symmetry mismatch between the protein cargo and the icosahedral encapsulin shell. The encapsulated ferritin decamers are offset from the interior face of the encapsulin shell. Using hydrogen/deuterium exchange mass spectrometry, we observed the dynamic behavior of the major fivefold pore in the encapsulin shell and show the pore opening via the movement of the encapsulin A-domain. These data will accelerate efforts to engineer the encapsulation of heterologous cargo proteins and to alter the permeability of the encapsulin shell via pore modifications. #1: Journal: Biorxiv / Year: 2021Title: Model of Haliangium ochraceum encapsulin from icosahedral single particle reconstruction Authors: Marles-Wright J / Basle A / Clarke DJ / Ross J | |||||||||
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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_12859.map.gz | 577 MB | EMDB map data format | |
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| Header (meta data) | emd-12859-v30.xml emd-12859.xml | 24 KB 24 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_12859_fsc.xml | 26.2 KB | Display | FSC data file |
| Images | emd_12859.png | 114.2 KB | ||
| Masks | emd_12859_msk_1.map | 729 MB | Mask map | |
| Filedesc metadata | emd-12859.cif.gz | 6.7 KB | ||
| Others | emd_12859_additional_1.map.gz emd_12859_half_map_1.map.gz emd_12859_half_map_2.map.gz | 26.7 MB 582.5 MB 582.5 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-12859 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-12859 | HTTPS FTP |
-Validation report
| Summary document | emd_12859_validation.pdf.gz | 770.1 KB | Display | EMDB validaton report |
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| Full document | emd_12859_full_validation.pdf.gz | 769.7 KB | Display | |
| Data in XML | emd_12859_validation.xml.gz | 27.5 KB | Display | |
| Data in CIF | emd_12859_validation.cif.gz | 37.1 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-12859 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-12859 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7oe2MC ![]() 7odwC ![]() 7oeuC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | |
| EM raw data | EMPIAR-10716 (Title: Cryo electron microscopy of single particles of the Haliangium ochraceum Encapsulin:encapsulated ferritin encapsulin nano compartmentData size: 1.7 TB Data #1: Multi-frame micrographs and particle sets for Haliangium ochraceum encapsulin:encapsulated ferritin reconstruction [micrographs - multiframe]) |
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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_12859.map.gz / Format: CCP4 / Size: 729 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Refine 3D map | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.652 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Mask #1
| File | emd_12859_msk_1.map | ||||||||||||
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-Additional map: Post processed masked map
| File | emd_12859_additional_1.map | ||||||||||||
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| Annotation | Post processed masked map | ||||||||||||
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-Half map: Half 1
| File | emd_12859_half_map_1.map | ||||||||||||
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| Annotation | Half 1 | ||||||||||||
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-Half map: Half 2
| File | emd_12859_half_map_2.map | ||||||||||||
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| Annotation | Half 2 | ||||||||||||
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Sample components
-Entire : Ternary complex of Haliangium ochraceum encapsulin and encapsulat...
| Entire | Name: Ternary complex of Haliangium ochraceum encapsulin and encapsulated ferritin proteins |
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| Components |
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-Supramolecule #1: Ternary complex of Haliangium ochraceum encapsulin and encapsulat...
| Supramolecule | Name: Ternary complex of Haliangium ochraceum encapsulin and encapsulated ferritin proteins type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 / Details: Complex produced by co-expression in E. coli |
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| Source (natural) | Organism: Haliangium ochraceum (bacteria) |
| Molecular weight | Theoretical: 1.8 MDa |
-Macromolecule #1: Linocin_M18 bacteriocin protein
| Macromolecule | Name: Linocin_M18 bacteriocin protein / type: protein_or_peptide / ID: 1 / Number of copies: 5 / Enantiomer: LEVO |
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| Source (natural) | Organism: Haliangium ochraceum (strain DSM 14365 / JCM 11303 / SMP-2) (bacteria)Strain: DSM 14365 / JCM 11303 / SMP-2 |
| Molecular weight | Theoretical: 28.844598 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MDLLKRHLAP IVPDAWSAID EEAKEIFQGH LAGRKLVDFR GPFGWEYAAV NTGELRPIDD TPEDVDMKLR QVQPLAEVRV PFTLDVTEL DSVARGATNP DLDDVARAAE RMVEAEDSAI FHGWAQAGIK GIVDSTPHEA LAVASVSDFP RAVLSAADTL R KAGVTGPY ...String: MDLLKRHLAP IVPDAWSAID EEAKEIFQGH LAGRKLVDFR GPFGWEYAAV NTGELRPIDD TPEDVDMKLR QVQPLAEVRV PFTLDVTEL DSVARGATNP DLDDVARAAE RMVEAEDSAI FHGWAQAGIK GIVDSTPHEA LAVASVSDFP RAVLSAADTL R KAGVTGPY ALVLGPKAYD DLFAATQDGY PVAKQVQRLV VDGPLVRANA LAGALVMSMR GGDYELTVGQ DLSIGYAFHD RS KVELFVA ESFTFRVLEP GAAVHLRYA UniProtKB: Type 1 encapsulin shell protein |
-Macromolecule #2: Haliangium ochraceum Encapsulated ferritin localisation sequence
| Macromolecule | Name: Haliangium ochraceum Encapsulated ferritin localisation sequence type: protein_or_peptide / ID: 2 / Number of copies: 5 / Enantiomer: LEVO |
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| Source (natural) | Organism: Haliangium ochraceum (strain DSM 14365 / JCM 11303 / SMP-2) (bacteria)Strain: DSM 14365 / JCM 11303 / SMP-2 |
| Molecular weight | Theoretical: 14.817368 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MSSEQLHEPA ELLSEETKNM HRALVTLIEE LEAVDWYQQR ADACSEPGLH DVLIHNKNEE VEHAMMTLEW IRRRSPVFDA HMRTYLFTE RPILELEEED TGSSSSVAAS PTSAPSHGSL GIGSLRQEGK ED UniProtKB: Encapsulated ferritin-like protein |
-Macromolecule #3: water
| Macromolecule | Name: water / type: ligand / ID: 3 / Number of copies: 154 / 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 | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 3 mg/mL | |||||||||
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| Buffer | pH: 8 Component:
Details: Solutions were prepared with MilliQ water and filtered using a 0.22 um filter. | |||||||||
| Grid | Model: Quantifoil / Material: GOLD / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 30 sec. / Pretreatment - Atmosphere: AIR | |||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 281 K / Instrument: FEI VITROBOT MARK IV Details: blot force -5, wait time 10 seconds and blot time of 3 seconds. | |||||||||
| Details | Sample mono disperse as determined by SEC |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Digitization - Dimensions - Width: 11520 pixel / Digitization - Dimensions - Height: 8184 pixel / Number grids imaged: 1 / Number real images: 8109 / Average exposure time: 1.0 sec. / Average electron dose: 40.509 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: OTHER / Imaging mode: BRIGHT FIELD |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
-Atomic model buiding 1
| Details | Initial fitting performed using chimera with real space refinement in Phenix. |
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| Refinement | Space: REAL / Protocol: RIGID BODY FIT / Overall B value: 86 / Target criteria: CC |
| Output model | ![]() PDB-7oe2: |
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About Yorodumi


Keywords
Haliangium ochraceum (bacteria)
Authors
United Kingdom, 1 items
Citation
UCSF Chimera















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