[English] 日本語
Yorodumi- EMDB-42488: Porcine epidemic diarrhea virus complete core polymerase complex -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-42488 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Title | Porcine epidemic diarrhea virus complete core polymerase complex | ||||||||||||
Map data | Single particle reconstruction of PEDV core polymerase complex | ||||||||||||
Sample |
| ||||||||||||
Keywords | Coronavirus / nsp12 / RNA polymerase / PEDV / REPLICATION / TRANSFERASE-RNA complex | ||||||||||||
Function / homology | Function and homology information host cell membrane / viral genome replication / host cell endoplasmic reticulum-Golgi intermediate compartment / 3'-5'-RNA exonuclease activity / 5'-3' DNA helicase activity / omega peptidase activity / symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of IRF3 activity / symbiont-mediated perturbation of host ubiquitin-like protein modification / endonuclease activity / mRNA (nucleoside-2'-O-)-methyltransferase activity ...host cell membrane / viral genome replication / host cell endoplasmic reticulum-Golgi intermediate compartment / 3'-5'-RNA exonuclease activity / 5'-3' DNA helicase activity / omega peptidase activity / symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of IRF3 activity / symbiont-mediated perturbation of host ubiquitin-like protein modification / endonuclease activity / mRNA (nucleoside-2'-O-)-methyltransferase activity / mRNA 5'-cap (guanine-N7-)-methyltransferase activity / cysteine-type deubiquitinase activity / RNA helicase activity / host cell perinuclear region of cytoplasm / viral protein processing / lyase activity / induction by virus of host autophagy / viral translational frameshifting / cysteine-type endopeptidase activity / RNA-dependent RNA polymerase activity / virus-mediated perturbation of host defense response / DNA-templated transcription / proteolysis / RNA binding / zinc ion binding / ATP binding / membrane Similarity search - Function | ||||||||||||
Biological species | Porcine epidemic diarrhea virus / synthetic construct (others) | ||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.4 Å | ||||||||||||
Authors | Anderson TK / Kirchdoerfer RN | ||||||||||||
Funding support | United States, 3 items
| ||||||||||||
Citation | Journal: bioRxiv / Year: 2023 Title: An alphacoronavirus polymerase structure reveals conserved co-factor functions. Authors: Thomas K Anderson / Peter J Hoferle / Kenneth W Lee / Joshua J Coon / Robert N Kirchdoerfer / Abstract: Coronaviruses are a diverse subfamily of viruses containing pathogens of humans and animals. This subfamily of viruses replicates their RNA genomes using a core polymerase complex composed of viral ...Coronaviruses are a diverse subfamily of viruses containing pathogens of humans and animals. This subfamily of viruses replicates their RNA genomes using a core polymerase complex composed of viral non-structural proteins: nsp7, nsp8 and nsp12. Most of our understanding of coronavirus molecular biology comes from the betacoronaviruses like SARS-CoV and SARS-CoV-2, the latter of which is the causative agent of COVID-19. In contrast, members of the alphacoronavirus genus are relatively understudied despite their importance in human and animal health. Here we have used cryo-electron microscopy to determine the structure of the alphacoronavirus porcine epidemic diarrhea virus (PEDV) core polymerase complex bound to RNA. Our structure shows an unexpected nsp8 stoichiometry in comparison to other published coronavirus polymerase structures. Biochemical analysis shows that the N-terminal extension of one nsp8 is not required for RNA synthesis for alpha and betacoronaviruses as previously hypothesized. Our work shows the importance of studying diverse coronaviruses to reveal aspects of coronavirus replication while also identifying areas of conservation to be targeted by antiviral drugs. | ||||||||||||
History |
|
-Structure visualization
Supplemental images |
---|
-Downloads & links
-EMDB archive
Map data | emd_42488.map.gz | 59.7 MB | EMDB map data format | |
---|---|---|---|---|
Header (meta data) | emd-42488-v30.xml emd-42488.xml | 22 KB 22 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_42488_fsc.xml | 8.5 KB | Display | FSC data file |
Images | emd_42488.png | 41.2 KB | ||
Masks | emd_42488_msk_1.map | 64 MB | Mask map | |
Filedesc metadata | emd-42488.cif.gz | 7.2 KB | ||
Others | emd_42488_half_map_1.map.gz emd_42488_half_map_2.map.gz | 59.5 MB 59.5 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-42488 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-42488 | HTTPS FTP |
-Validation report
Summary document | emd_42488_validation.pdf.gz | 935.7 KB | Display | EMDB validaton report |
---|---|---|---|---|
Full document | emd_42488_full_validation.pdf.gz | 935.3 KB | Display | |
Data in XML | emd_42488_validation.xml.gz | 16.4 KB | Display | |
Data in CIF | emd_42488_validation.cif.gz | 21.1 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42488 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42488 | HTTPS FTP |
-Related structure data
Related structure data | 8urbMC 8g6rC M: atomic model generated by this map C: citing same article (ref.) |
---|---|
Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
---|---|
Related items in Molecule of the Month |
-Map
File | Download / File: emd_42488.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Annotation | Single particle reconstruction of PEDV core polymerase complex | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.064 Å | ||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
|
-Supplemental data
-Mask #1
File | emd_42488_msk_1.map | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-Half map: #2
File | emd_42488_half_map_1.map | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-Half map: #1
File | emd_42488_half_map_2.map | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-Sample components
-Entire : Core polymerase complex of the porcine epidemic diarrhea virus co...
Entire | Name: Core polymerase complex of the porcine epidemic diarrhea virus composed of nsp12, nsp7, nsp8, and a short RNA substrate |
---|---|
Components |
|
-Supramolecule #1: Core polymerase complex of the porcine epidemic diarrhea virus co...
Supramolecule | Name: Core polymerase complex of the porcine epidemic diarrhea virus composed of nsp12, nsp7, nsp8, and a short RNA substrate type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#5 |
---|---|
Source (natural) | Organism: Porcine epidemic diarrhea virus |
Molecular weight | Theoretical: 185 KDa |
-Macromolecule #1: nsp12
Macromolecule | Name: nsp12 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: Porcine epidemic diarrhea virus |
Molecular weight | Theoretical: 108.994758 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: STDMAYLNRV RGSSAARLEP CNGTDTQHVY RAFDIYNKDV ACLGKFLKVN CVRLKNLDKH DAFYVVKRCT KSAMEHEQSI YSRLEKCGA VAEHDFFTWK DGRAIYGNVC RKDLTEYTMM DLCYALRNFD ENNCDVLKSI LIKVGACEES YFNNKVWFDP V ENEDIHRV ...String: STDMAYLNRV RGSSAARLEP CNGTDTQHVY RAFDIYNKDV ACLGKFLKVN CVRLKNLDKH DAFYVVKRCT KSAMEHEQSI YSRLEKCGA VAEHDFFTWK DGRAIYGNVC RKDLTEYTMM DLCYALRNFD ENNCDVLKSI LIKVGACEES YFNNKVWFDP V ENEDIHRV YALLGTIVSR AMLKCVKFCD AMVEQGIVGV VTLDNQDLNG DFYDFGDFTC SIKGMGIPIC TSYYSYMMPV MG MTNCLAS ECFVKSDIFG EDFKSYDLLE YDFTEHKTAL FNKYFKYWGL QYHPNCVDCS DEQCIVHCAN FNTLFSTTIP ITA FGPLCR KCWIDGVPLV TTAGYHFKQL GIVWNNDLNL HSSRLSINEL LQFCSDPALL IASSPALVDQ RTVCFSVAAL GTGM TNQTV KPGHFNKEFY DFLLEQGFFS EGSELTLKHF FFAQKGDAAV KDFDYYRYNR PTVLDICQAR VVYQIVQRYF DIYEG GCIT AKEVVVTNLN KSAGYPLNKF GKAGLYYESL SYEEQDELYA YTKRNILPTM TQLNLKYAIS GKERARTVGG VSLLST MTT RQYHQKHLKS IVNTRGASVV IGTTKFYGGW DNMLKNLIDG VENPCLMGWD YPKCDRALPN MIRMISAMIL GSKHTTC CS STDRFFRLCN ELAQVLTEVV YSNGGFYLKP GGTTSGDATT AYANSVFNIF QAVSANVNKL LSVDSNVCHN LEVKQLQR K LYECCYRSTT VDDQFVVEYY GYLRKHFSMM ILSDDGVVCY NNDYASLGYV ADLNAFKAVL YYQNNVFMSA SKCWIEPDI NKGPHEFCSQ HTMQIVDKDG TYYLPYPDPS RILSAGVFVD DVVKTDAVVL LERYVSLAID AYPLSKHENP EYKKVFYVLL DWVKHLYKT LNAGVLESFS VTLLEDSTAK FWDESFYANM YEKSAVLQEN LYFQGSWSHP QFEKGGSGSS WSHPQFEK UniProtKB: ORF1ab polyprotein |
-Macromolecule #2: nsp8
Macromolecule | Name: nsp8 / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: Porcine epidemic diarrhea virus |
Molecular weight | Theoretical: 21.716838 KDa |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) |
Sequence | String: SVASTYVGLP SYVIYENARQ QYEDAVNNGS PPQLVKQLRH AMNVAKSEFD REASTQRKLD RMAEQAAAQM YKEARAVNRK SKVVSAMHS LLFGMLRRLD MSSVDTILNL AKDGVVPLSV IPAVSATKLN IVTSDIDSYN RIQREGCVHY AGTIWNIIDI K DNDGKVVH ...String: SVASTYVGLP SYVIYENARQ QYEDAVNNGS PPQLVKQLRH AMNVAKSEFD REASTQRKLD RMAEQAAAQM YKEARAVNRK SKVVSAMHS LLFGMLRRLD MSSVDTILNL AKDGVVPLSV IPAVSATKLN IVTSDIDSYN RIQREGCVHY AGTIWNIIDI K DNDGKVVH VKEVTAQNAE SLSWPLVLGC ERIVKLQ UniProtKB: ORF1ab polyprotein |
-Macromolecule #3: nsp7
Macromolecule | Name: nsp7 / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: Porcine epidemic diarrhea virus |
Molecular weight | Theoretical: 9.230511 KDa |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) |
Sequence | String: SKLTDIKCSN VVLLGCLSSM NVSANSTEWA YCVDLHNKIN LCNDPEKAQE MLLALLAFFL SKNSAFGLDD LLESYFNDNS MLQ UniProtKB: ORF1ab polyprotein |
-Macromolecule #4: RNA (33-MER)
Macromolecule | Name: RNA (33-MER) / type: rna / ID: 4 / Number of copies: 1 |
---|---|
Source (natural) | Organism: synthetic construct (others) |
Molecular weight | Theoretical: 10.468266 KDa |
Sequence | String: CAUUCUCCUA AGAAGCUAUU AAAAUCACAG AUU |
-Macromolecule #5: RNA (55-MER)
Macromolecule | Name: RNA (55-MER) / type: rna / ID: 5 / Number of copies: 1 |
---|---|
Source (natural) | Organism: synthetic construct (others) |
Molecular weight | Theoretical: 17.740572 KDa |
Sequence | String: CAGUGUCAUG GAAAAACAGA AAAAUCUGUG AUUUUAAUAG CUUCUUAGGA GAAUG |
-Macromolecule #6: ZINC ION
Macromolecule | Name: ZINC ION / type: ligand / ID: 6 / Number of copies: 2 / Formula: ZN |
---|---|
Molecular weight | Theoretical: 65.409 Da |
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 1 mg/mL | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Buffer | pH: 7.5 Component:
| ||||||||||||||||||
Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 20 sec. | ||||||||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | FEI TALOS ARCTICA |
---|---|
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 60.0 e/Å2 |
Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 70.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.5 µm |
Experimental equipment | Model: Talos Arctica / Image courtesy: FEI Company |