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Yorodumi- EMDB-42087: Representative tomogram of Enterococcus faecium SagA deletion strain -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-42087 | |||||||||
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Title | Representative tomogram of Enterococcus faecium SagA deletion strain | |||||||||
Map data | Representative tomogram of Enterococcus faecium SagA deletion strain | |||||||||
Sample |
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Keywords | Bacteria / cancer therapy / HYDROLASE | |||||||||
Biological species | Enterococcus faecium (bacteria) | |||||||||
Method | electron tomography / cryo EM | |||||||||
Authors | Hang HC / Park D | |||||||||
Funding support | United States, 1 items
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Citation | Journal: bioRxiv / Year: 2024 Title: Secreted antigen A peptidoglycan hydrolase is essential for cell separation and priming of immune checkpoint inhibitor therapy. Authors: Steven Klupt / Kyong Tkhe Fam / Xing Zhang / Pavan Kumar Chodisetti / Abeera Mehmood / Tumara Boyd / Danielle Grotjahn / Donghyun Park / Howard C Hang / Abstract: is a microbiota species in humans that can modulate host immunity, but has also acquired antibiotic resistance and is a major cause of hospital-associated infections. Notably, diverse strains of ... is a microbiota species in humans that can modulate host immunity, but has also acquired antibiotic resistance and is a major cause of hospital-associated infections. Notably, diverse strains of produce SagA, a highly conserved peptidoglycan hydrolase that is sufficient to promote intestinal immunity and immune checkpoint inhibitor antitumor activity. However, the functions of SagA in were unknown. Here we report that deletion of impaired growth and resulted in bulged and clustered enterococci due to defective peptidoglycan cleavage and cell separation. Moreover, Δ showed increased antibiotic sensitivity, yielded lower levels of active muropeptides, displayed reduced activation of the peptidoglycan pattern-recognition receptor NOD2, and failed to promote cancer immunotherapy. Importantly, plasmid-based expression of SagA, but not its catalytically-inactive mutant, restored Δ growth, production of active muropeptides and NOD2 activation. SagA is therefore essential for growth, stress resistance and activation of host immunity. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_42087.map.gz | 157 MB | EMDB map data format | |
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Header (meta data) | emd-42087-v30.xml emd-42087.xml | 9.7 KB 9.7 KB | Display Display | EMDB header |
Images | emd_42087.png | 177 KB | ||
Filedesc metadata | emd-42087.cif.gz | 3.6 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-42087 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-42087 | HTTPS FTP |
-Validation report
Summary document | emd_42087_validation.pdf.gz | 427.8 KB | Display | EMDB validaton report |
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Full document | emd_42087_full_validation.pdf.gz | 427.4 KB | Display | |
Data in XML | emd_42087_validation.xml.gz | 4.2 KB | Display | |
Data in CIF | emd_42087_validation.cif.gz | 4.6 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42087 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42087 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_42087.map.gz / Format: CCP4 / Size: 175.4 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||
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Annotation | Representative tomogram of Enterococcus faecium SagA deletion strain | ||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. generated in cubic-lattice coordinate | ||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 21.1 Å | ||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Sample components
-Entire : Enterococcus faecium WT Com15
Entire | Name: Enterococcus faecium WT Com15 |
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Components |
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-Supramolecule #1: Enterococcus faecium WT Com15
Supramolecule | Name: Enterococcus faecium WT Com15 / type: cell / ID: 1 / Parent: 0 |
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Source (natural) | Organism: Enterococcus faecium (bacteria) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | electron tomography |
Aggregation state | cell |
-Sample preparation
Buffer | pH: 7 |
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Vitrification | Cryogen name: ETHANE |
Sectioning | Focused ion beam - Instrument: OTHER / Focused ion beam - Ion: OTHER / Focused ion beam - Voltage: 30 / Focused ion beam - Current: 10 / Focused ion beam - Duration: 30 / Focused ion beam - Temperature: 93 K / Focused ion beam - Initial thickness: 500 / Focused ion beam - Final thickness: 150 Focused ion beam - Details: The value given for _em_focused_ion_beam.instrument is Aquilos. This is not in a list of allowed values {'OTHER', 'DB235'} so OTHER is written into the XML file. |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 3.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: OTHER / Nominal defocus max: 6.0 µm / Nominal defocus min: 4.0 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Number images used: 37 |
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