+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-29326 | |||||||||||||||
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Title | Structure of RdrA from Streptococcus suis RADAR defense system | |||||||||||||||
Map data | ||||||||||||||||
Sample |
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Keywords | RADAR / ATPase / RdrA / antiphage system / IMMUNE SYSTEM | |||||||||||||||
Function / homology | KAP family P-loop domain / KAP family P-loop domain / P-loop containing nucleoside triphosphate hydrolase / KAP NTPase domain-containing protein Function and homology information | |||||||||||||||
Biological species | Streptococcus suis (bacteria) | |||||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.5 Å | |||||||||||||||
Authors | Duncan-Lowey B / Johnson AG / Rawson S / Mayer ML / Kranzusch PJ | |||||||||||||||
Funding support | United States, 4 items
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Citation | Journal: Cell / Year: 2023 Title: Cryo-EM structure of the RADAR supramolecular anti-phage defense complex. Authors: Brianna Duncan-Lowey / Nitzan Tal / Alex G Johnson / Shaun Rawson / Megan L Mayer / Shany Doron / Adi Millman / Sarah Melamed / Taya Fedorenko / Assaf Kacen / Alexander Brandis / Tevie ...Authors: Brianna Duncan-Lowey / Nitzan Tal / Alex G Johnson / Shaun Rawson / Megan L Mayer / Shany Doron / Adi Millman / Sarah Melamed / Taya Fedorenko / Assaf Kacen / Alexander Brandis / Tevie Mehlman / Gil Amitai / Rotem Sorek / Philip J Kranzusch / Abstract: RADAR is a two-protein bacterial defense system that was reported to defend against phage by "editing" messenger RNA. Here, we determine cryo-EM structures of the RADAR defense complex, revealing ...RADAR is a two-protein bacterial defense system that was reported to defend against phage by "editing" messenger RNA. Here, we determine cryo-EM structures of the RADAR defense complex, revealing RdrA as a heptameric, two-layered AAA+ ATPase and RdrB as a dodecameric, hollow complex with twelve surface-exposed deaminase active sites. RdrA and RdrB join to form a giant assembly up to 10 MDa, with RdrA docked as a funnel over the RdrB active site. Surprisingly, our structures reveal an RdrB active site that targets mononucleotides. We show that RdrB catalyzes ATP-to-ITP conversion in vitro and induces the massive accumulation of inosine mononucleotides during phage infection in vivo, limiting phage replication. Our results define ATP mononucleotide deamination as a determinant of RADAR immunity and reveal supramolecular assembly of a nucleotide-modifying machine as a mechanism of anti-phage defense. | |||||||||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_29326.map.gz | 230.1 MB | EMDB map data format | |
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Header (meta data) | emd-29326-v30.xml emd-29326.xml | 15.2 KB 15.2 KB | Display Display | EMDB header |
Images | emd_29326.png | 75.4 KB | ||
Filedesc metadata | emd-29326.cif.gz | 5.9 KB | ||
Others | emd_29326_half_map_1.map.gz emd_29326_half_map_2.map.gz | 226.4 MB 226.4 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-29326 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-29326 | HTTPS FTP |
-Validation report
Summary document | emd_29326_validation.pdf.gz | 915.6 KB | Display | EMDB validaton report |
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Full document | emd_29326_full_validation.pdf.gz | 915.2 KB | Display | |
Data in XML | emd_29326_validation.xml.gz | 15.7 KB | Display | |
Data in CIF | emd_29326_validation.cif.gz | 18.5 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-29326 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-29326 | HTTPS FTP |
-Related structure data
Related structure data | 8fnuMC 8fntC 8fnvC 8fnwC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_29326.map.gz / Format: CCP4 / Size: 244.1 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: 1.1 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_29326_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_29326_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : RdrA heptameric complex
Entire | Name: RdrA heptameric complex |
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Components |
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-Supramolecule #1: RdrA heptameric complex
Supramolecule | Name: RdrA heptameric complex / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Streptococcus suis (bacteria) |
-Macromolecule #1: KAP NTPase domain-containing protein
Macromolecule | Name: KAP NTPase domain-containing protein / type: protein_or_peptide / ID: 1 / Number of copies: 7 / Enantiomer: LEVO |
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Source (natural) | Organism: Streptococcus suis (bacteria) |
Molecular weight | Theoretical: 106.413305 KDa |
Recombinant expression | Organism: Escherichia coli (E. coli) |
Sequence | String: MTKINWEKYK KVIKKEFSEK EETEEVKNYI FSSQLDKVNL ILEHMDTVGG IHSRNIAITG DRGTGKTSFI ETLKLVLEKQ NYYVFDIVS PTVLSSHLNI LEIVISSIYR EIDQFIDSHD VHDRGRLIQH LKKVMNAIAV EKKQSDYFKQ SKPEIEMLTD L SHRTFLDE ...String: MTKINWEKYK KVIKKEFSEK EETEEVKNYI FSSQLDKVNL ILEHMDTVGG IHSRNIAITG DRGTGKTSFI ETLKLVLEKQ NYYVFDIVS PTVLSSHLNI LEIVISSIYR EIDQFIDSHD VHDRGRLIQH LKKVMNAIAV EKKQSDYFKQ SKPEIEMLTD L SHRTFLDE EIKELFCYFK KVLNNRQDSC KEVIKDLVLI IDDLDLVENN LVYDLLRDIQ HYLDSQLIVI FAYKEGQLEQ SM FEHLAKG NEALLNHGVI DSNAIFGQIE RFLTKLVPLS NRIPLFKQDE LLNKTIGEFL ASLDPSYGVG ENLEFITKDS EKN KNNLTI REWFYESIFY RTNLKLDPID IREEASRLMP KTLREMVQLC EELHSMQVIT RSMDKLAGVE GLRKNIGAFR RYIG YKNST YFNLATMEFF QKWELAESHQ ANYLAYHFLM SYYQESFEQN QKLGYPLNLS KSGYPLTLRT MEPYNITLGD IYALM EELK YTEGISADTY YIVYILKVYY SLRLSELLYN VVLHHKLFVH VKEEATTFYM ATSTEELQIE KNHEQEATKL TDKEYR EHI MTAIEKVPAL QAYLELVNAQ FMPQNFNYDR SGSRDDDFYL ISWLKDDDLP EYSRLFKSLF LNSEVAAKGQ IQRNIGK RE SVFRYRNLYS YLPLQLTSAT FYKIDFLAFA IKADLLMYNV VRFVEEEGDT IPYFMSNMFH IDVFVRHNYN ENNNKGKF A YIAKQIVFGL WQGSNQRAHD LKHWYKSFDT VFGTKIEALH LLVDIAEQIK ISDKQTTDVS ALSEEQKRDE QAKKVAEKL AAIYHHIGMS RILSRLHQLP FIAEIKSNKE LLQHFSEAIV KLEKYASDTI NVGNLSQFRE SLKKIGQTYP SIQVLVDKLH RKQKLYVEF IQDFIETVNK LGEADESN UniProtKB: KAP NTPase domain-containing protein |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.5 Component:
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Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % |
-Electron microscopy
Microscope | FEI TALOS ARCTICA |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 42.02 e/Å2 |
Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: OTHER / Imaging mode: OTHER / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.7000000000000001 µm |
Experimental equipment | Model: Talos Arctica / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: NONE |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 2.5 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 193305 |
Initial angle assignment | Type: OTHER |
Final angle assignment | Type: OTHER |