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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | Cryo-EM map of DdmDE(1:1) complex bound with DNA | |||||||||
Map data | Cryo-EM map of DdmDE(1:1) complex bound with DNA | |||||||||
Sample |
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Keywords | defense system / DNA defense modules (Ddm) / DdmDE / bacteria / anti-plasmid / IMMUNE SYSTEM | |||||||||
| Biological species | ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.32 Å | |||||||||
Authors | Shen ZF / Yang XY / Fu TM | |||||||||
| Funding support | 1 items
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Citation | Journal: Cell / Year: 2024Title: DdmDE eliminates plasmid invasion by DNA-guided DNA targeting. Authors: Xiao-Yuan Yang / Zhangfei Shen / Chen Wang / Kotaro Nakanishi / Tian-Min Fu / ![]() Abstract: Horizontal gene transfer is a key driver of bacterial evolution, but it also presents severe risks to bacteria by introducing invasive mobile genetic elements. To counter these threats, bacteria have ...Horizontal gene transfer is a key driver of bacterial evolution, but it also presents severe risks to bacteria by introducing invasive mobile genetic elements. To counter these threats, bacteria have developed various defense systems, including prokaryotic Argonautes (pAgos) and the DNA defense module DdmDE system. Through biochemical analysis, structural determination, and in vivo plasmid clearance assays, we elucidate the assembly and activation mechanisms of DdmDE, which eliminates small, multicopy plasmids. We demonstrate that DdmE, a pAgo-like protein, acts as a catalytically inactive, DNA-guided, DNA-targeting defense module. In the presence of guide DNA, DdmE targets plasmids and recruits a dimeric DdmD, which contains nuclease and helicase domains. Upon binding to DNA substrates, DdmD transitions from an autoinhibited dimer to an active monomer, which then translocates along and cleaves the plasmids. Together, our findings reveal the intricate mechanisms underlying DdmDE-mediated plasmid clearance, offering fundamental insights into bacterial defense systems against plasmid invasions. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_44563.map.gz | 86.1 MB | EMDB map data format | |
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| Header (meta data) | emd-44563-v30.xml emd-44563.xml | 12.9 KB 12.9 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_44563_fsc.xml | 9.5 KB | Display | FSC data file |
| Images | emd_44563.png | 123.9 KB | ||
| Filedesc metadata | emd-44563.cif.gz | 3.8 KB | ||
| Others | emd_44563_half_map_1.map.gz emd_44563_half_map_2.map.gz | 84.6 MB 84.6 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-44563 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-44563 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_44563.map.gz / Format: CCP4 / Size: 91.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Cryo-EM map of DdmDE(1:1) complex bound with DNA | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.09 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: Half Map A
| File | emd_44563_half_map_1.map | ||||||||||||
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| Annotation | Half Map A | ||||||||||||
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| Density Histograms |
-Half map: Half Map B
| File | emd_44563_half_map_2.map | ||||||||||||
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| Annotation | Half Map B | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : V. cholerae DdmDE complex bound with DNA
| Entire | Name: V. cholerae DdmDE complex bound with DNA |
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| Components |
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-Supramolecule #1: V. cholerae DdmDE complex bound with DNA
| Supramolecule | Name: V. cholerae DdmDE complex bound with DNA / type: complex / ID: 1 / Parent: 0 |
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| Source (natural) | Organism: ![]() |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 8 |
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| Vitrification | Cryogen name: ETHANE |
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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) / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.5 µm / Nominal defocus min: 0.5 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Processing
FIELD EMISSION GUN

