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Yorodumi- EMDB-22381: Structure of the activated Roq1 resistosome directly recognizing ... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-22381 | |||||||||
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Title | Structure of the activated Roq1 resistosome directly recognizing the pathogen effector XopQ | |||||||||
Map data | Structure of the activated Roq1 resistosome directly recognizing the pathogen effector XopQ | |||||||||
Sample |
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Keywords | Resistosome / Plant Immunity / Effector / LRR / TIR / NB-ARC / IMMUNE SYSTEM | |||||||||
Function / homology | Function and homology information ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase / NAD+ nucleosidase activity / NAD+ nucleotidase, cyclic ADP-ribose generating / Hydrolases; Glycosylases; Hydrolysing N-glycosyl compounds / ADP binding / defense response / signal transduction Similarity search - Function | |||||||||
Biological species | Nicotiana benthamiana (plant) / Xanthomonas euvesicatoria (bacteria) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.8 Å | |||||||||
Authors | Martin R / Qi T | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Science / Year: 2020 Title: Structure of the activated ROQ1 resistosome directly recognizing the pathogen effector XopQ. Authors: Raoul Martin / Tiancong Qi / Haibo Zhang / Furong Liu / Miles King / Claire Toth / Eva Nogales / Brian J Staskawicz / Abstract: Plants and animals detect pathogen infection using intracellular nucleotide-binding leucine-rich repeat receptors (NLRs) that directly or indirectly recognize pathogen effectors and activate an ...Plants and animals detect pathogen infection using intracellular nucleotide-binding leucine-rich repeat receptors (NLRs) that directly or indirectly recognize pathogen effectors and activate an immune response. How effector sensing triggers NLR activation remains poorly understood. Here we describe the 3.8-angstrom-resolution cryo-electron microscopy structure of the activated ROQ1 (recognition of XopQ 1), an NLR native to with a Toll-like interleukin-1 receptor (TIR) domain bound to the effector XopQ ( outer protein Q). ROQ1 directly binds to both the predicted active site and surface residues of XopQ while forming a tetrameric resistosome that brings together the TIR domains for downstream immune signaling. Our results suggest a mechanism for the direct recognition of effectors by NLRs leading to the oligomerization-dependent activation of a plant resistosome and signaling by the TIR domain. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_22381.map.gz | 395.7 MB | EMDB map data format | |
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Header (meta data) | emd-22381-v30.xml emd-22381.xml | 16 KB 16 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_22381_fsc.xml | 17.1 KB | Display | FSC data file |
Images | emd_22381.png | 105.5 KB | ||
Filedesc metadata | emd-22381.cif.gz | 6.7 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-22381 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-22381 | HTTPS FTP |
-Validation report
Summary document | emd_22381_validation.pdf.gz | 703.2 KB | Display | EMDB validaton report |
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Full document | emd_22381_full_validation.pdf.gz | 702.8 KB | Display | |
Data in XML | emd_22381_validation.xml.gz | 15.1 KB | Display | |
Data in CIF | emd_22381_validation.cif.gz | 20.7 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-22381 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-22381 | HTTPS FTP |
-Related structure data
Related structure data | 7jlvMC 7jluC 7jlxC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_22381.map.gz / Format: CCP4 / Size: 421.9 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Structure of the activated Roq1 resistosome directly recognizing the pathogen effector XopQ | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.9386 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : Roq1
Entire | Name: Roq1 |
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Components |
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-Supramolecule #1: Roq1
Supramolecule | Name: Roq1 / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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Source (natural) | Organism: Nicotiana benthamiana (plant) |
Molecular weight | Theoretical: 49.819 KDa |
-Supramolecule #2: XopQ
Supramolecule | Name: XopQ / type: complex / ID: 2 / Parent: 1 / Macromolecule list: #1 |
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Source (natural) | Organism: Xanthomonas euvesicatoria (bacteria) |
-Macromolecule #1: Disease resistance protein Roq1
Macromolecule | Name: Disease resistance protein Roq1 / type: protein_or_peptide / ID: 1 / Number of copies: 4 / Enantiomer: LEVO / EC number: ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase |
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Source (natural) | Organism: Nicotiana benthamiana (plant) |
Molecular weight | Theoretical: 150.648391 KDa |
Recombinant expression | Organism: Nicotiana benthamiana (plant) |
Sequence | String: MLTSSSHHGR SYDVFLSFRG EDTRKTFVGH LFNALIEKGI HTFMDDKELK RGKSISSELM KAIGESRFAV VVFSKNYASS TWCLEELVK ILEIHEKFEL IVVPVFYDVD PSTVRKQNGE YAVCFTKFEA NLVDDRDKVL RWREALTKVA NISGHDLRNT Y NGDESKCI ...String: MLTSSSHHGR SYDVFLSFRG EDTRKTFVGH LFNALIEKGI HTFMDDKELK RGKSISSELM KAIGESRFAV VVFSKNYASS TWCLEELVK ILEIHEKFEL IVVPVFYDVD PSTVRKQNGE YAVCFTKFEA NLVDDRDKVL RWREALTKVA NISGHDLRNT Y NGDESKCI QQILKDIFDK FCFSISITNR DLVGIESQIK KLSSLLRMDL KGVRLVGIWG MGGVGKTTAA RALFNRYYQN FE SACFLED VKEYLQHHTL LYLQKTLLSK LLKVEFVDCT DTEEMCVILK RRLCSKKVLV VLDDVNHNDQ LDKLVGAEDW FGS GSRIVI TTRDMKLLKN HDVHETYEIK VLEKDEAIEL FNLHAFKRSS PEKEFKELLN LVVDYTGGLP LALKVLGSLL YKED LDVWI STIDRLKDNP EGEIMATLKI SFDGLRDYEK SIFLDIACFF RGYNQRDMTA LFHASGFHPV LGVKTLVEKS LIFIL EDKI QMHDLMQEMG RQIAVQESPM RRIYRPEDVK DACIGDMRKE AIEGLLLTEP EQFEEGELEY MYSAEALKKT RRLRIL VKE YYNRGFDEPV AYLPNSLLWL EWRNYSSNSF PSNFEPSKLV YLTMKGSSII ELWNGAKRLA FLTTLDLSYC HKLIQTP DF RMITNLERLI LSSCDALVEV HPSVGFLKNL ILLNMDHCIS LERLPAIIQS ECLEVLDLNY CFNLKMFPEV ERNMTHLK K LDLTSTGIRE LPASIEHLSS LENLQMHSCN QLVSLPSSIW RFRNLKISEC EKLGSLPEIH GNSNCTRELI LKLVSIKEL PTSIGNLTSL NFLEICNCKT ISSLSSSIWG LTSLTTLKLL DCRKLKNLPG IPNAINHLSG HGLQLLLTLE QPTIYERLDL LRIIDMSWC SCISSLPHNI WMLKFLRILC ISYCSRLEYL PENLGHLEHL EELLADGTGI LRLPSSVARL NKLEVLSFRK K FAIGPKVQ YSSSMLNLPD DVFGSLGSLG SVVKLNLSGN GFCNLPETMN QLFCLEYLDI TFCQRLEALP ELPPSIKELY VD EHLALRI MEDLVIKCKE LNLIAVTKIE YQNFYRWLDS IWSDVSELLE NSQKQQLDDM LQLIPFSYLS TAKREEVLKI VIH GTRIPE WFRWQDRSAT TMSVNLPEYW YTENFLGFAI CCSCCFYHSA RSYDVEFEGS MHHYNYDSSY WKEYEEPSYD FYER DSIEI TAKLTPRHKG MRTEELKKVC SFSMNVLRRA TAVPNMCFAF FPFNSLCHIS NLQANNPNDY GIFETCLSPG DIRHR GKQW GFNLVYKDET GGSVTHEMLI NR UniProtKB: Disease resistance protein Roq1 |
-Macromolecule #2: ADENOSINE-5'-TRIPHOSPHATE
Macromolecule | Name: ADENOSINE-5'-TRIPHOSPHATE / type: ligand / ID: 2 / Number of copies: 4 / Formula: ATP |
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Molecular weight | Theoretical: 507.181 Da |
Chemical component information | ChemComp-ATP: |
-Macromolecule #3: MAGNESIUM ION
Macromolecule | Name: MAGNESIUM ION / type: ligand / ID: 3 / Number of copies: 4 / Formula: MG |
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Molecular weight | Theoretical: 24.305 Da |
-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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Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 400 / Support film - Material: CARBON / Support film - topology: CONTINUOUS / Pretreatment - Type: PLASMA CLEANING | ||||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277.15 K / Instrument: FEI VITROBOT MARK IV / Details: 10 sec blot. Blot Force 10. 90 min incubation.. | ||||||||||||||
Details | Sample was monodisperse. |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Energy filter - Name: GIF Bioquantum |
Image recording | Film or detector model: GATAN K3 (6k x 4k) / Number grids imaged: 1 / Number real images: 11134 / Average electron dose: 50.0 e/Å2 Details: Images were collected as dose-fractionated movie frames. |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Calibrated magnification: 80879 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: -2.5 µm / Nominal defocus min: -0.9 µm |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |