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Yorodumi- PDB-6wen: Crystal Structure of ADP ribose phosphatase of NSP3 from SARS-CoV... -
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Basic information
| Entry | Database: PDB / ID: 6wen | ||||||
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| Title | Crystal Structure of ADP ribose phosphatase of NSP3 from SARS-CoV-2 in the apo form | ||||||
Components | Non-structural protein 3 | ||||||
Keywords | HYDROLASE / SARS Coronavirus / Structural Genomics / Center for Structural Genomics of Infectious Diseases / CSGID / VIRAL PROTEIN | ||||||
| Function / homology | Function and homology informationprotein guanylyltransferase activity / RNA endonuclease activity producing 3'-phosphomonoesters, hydrolytic mechanism / mRNA guanylyltransferase activity / 5'-3' RNA helicase activity / Lyases; Phosphorus-oxygen lyases / Assembly of the SARS-CoV-2 Replication-Transcription Complex (RTC) / symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of TBK1 activity / Maturation of replicase proteins / TRAF3-dependent IRF activation pathway / ISG15-specific peptidase activity ...protein guanylyltransferase activity / RNA endonuclease activity producing 3'-phosphomonoesters, hydrolytic mechanism / mRNA guanylyltransferase activity / 5'-3' RNA helicase activity / Lyases; Phosphorus-oxygen lyases / Assembly of the SARS-CoV-2 Replication-Transcription Complex (RTC) / symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of TBK1 activity / Maturation of replicase proteins / TRAF3-dependent IRF activation pathway / ISG15-specific peptidase activity / Transcription of SARS-CoV-2 sgRNAs / Translation of Replicase and Assembly of the Replication Transcription Complex / snRNP Assembly / Replication of the SARS-CoV-2 genome / Hydrolases; Acting on ester bonds; Exoribonucleases producing 5'-phosphomonoesters / host cell endoplasmic reticulum-Golgi intermediate compartment / double membrane vesicle viral factory outer membrane / SARS coronavirus main proteinase / 5'-3' DNA helicase activity / 3'-5'-RNA exonuclease activity / host cell endosome / symbiont-mediated degradation of host mRNA / mRNA guanylyltransferase / symbiont-mediated suppression of host ISG15-protein conjugation / G-quadruplex RNA binding / symbiont-mediated suppression of host toll-like receptor signaling pathway / symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of IRF3 activity / omega peptidase activity / SARS-CoV-2 modulates host translation machinery / mRNA (guanine-N7)-methyltransferase / methyltransferase cap1 / host cell Golgi apparatus / symbiont-mediated suppression of host NF-kappaB cascade / symbiont-mediated perturbation of host ubiquitin-like protein modification / DNA helicase / methyltransferase cap1 activity / ubiquitinyl hydrolase 1 / cysteine-type deubiquitinase activity / mRNA 5'-cap (guanine-N7-)-methyltransferase activity / Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases / single-stranded RNA binding / regulation of autophagy / host cell perinuclear region of cytoplasm / viral protein processing / lyase activity / host cell endoplasmic reticulum membrane / RNA helicase / symbiont-mediated suppression of host type I interferon-mediated signaling pathway / symbiont-mediated suppression of host gene expression / copper ion binding / viral translational frameshifting / symbiont-mediated activation of host autophagy / RNA-directed RNA polymerase / cysteine-type endopeptidase activity / viral RNA genome replication / RNA-directed RNA polymerase activity / DNA-templated transcription / lipid binding / host cell nucleus / SARS-CoV-2 activates/modulates innate and adaptive immune responses / ATP hydrolysis activity / proteolysis / RNA binding / zinc ion binding / ATP binding / membrane Similarity search - Function | ||||||
| Biological species | ![]() | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.35 Å | ||||||
Authors | Michalska, K. / Stols, L. / Jedrzejczak, R. / Endres, M. / Babnigg, G. / Kim, Y. / Joachimiak, A. / Center for Structural Genomics of Infectious Diseases (CSGID) | ||||||
| Funding support | United States, 1items
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Citation | Journal: Iucrj / Year: 2020Title: Crystal structures of SARS-CoV-2 ADP-ribose phosphatase: from the apo form to ligand complexes. Authors: Michalska, K. / Kim, Y. / Jedrzejczak, R. / Maltseva, N.I. / Stols, L. / Endres, M. / Joachimiak, A. | ||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 6wen.cif.gz | 96.1 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb6wen.ent.gz | 71.5 KB | Display | PDB format |
| PDBx/mmJSON format | 6wen.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 6wen_validation.pdf.gz | 399.5 KB | Display | wwPDB validaton report |
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| Full document | 6wen_full_validation.pdf.gz | 399.5 KB | Display | |
| Data in XML | 6wen_validation.xml.gz | 11.2 KB | Display | |
| Data in CIF | 6wen_validation.cif.gz | 17.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/we/6wen ftp://data.pdbj.org/pub/pdb/validation_reports/we/6wen | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 6vxsC ![]() 6w02C ![]() 6w6yC ![]() 6wcfSC C: citing same article ( S: Starting model for refinement |
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| Similar structure data | |
| Other databases |
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Links
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Assembly
| Deposited unit | ![]()
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| Unit cell |
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| Components on special symmetry positions |
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Components
| #1: Protein | Mass: 18275.771 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: rep, 1a-1b / Plasmid: pET11a / Production host: ![]() References: UniProt: P0DTD1, EC: 3.4.19.121, Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases |
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| #2: Chemical | ChemComp-CL / |
| #3: Water | ChemComp-HOH / |
| Has ligand of interest | N |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 2.11 Å3/Da / Density % sol: 41.71 % |
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| Crystal grow | Temperature: 289 K / Method: vapor diffusion, sitting drop / pH: 9 Details: 34.3% PEG 5000 MME, 150 mM AMPD/Tris, pH 9.0, 30 mM K/NA tartrate |
-Data collection
| Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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| Diffraction source | Source: SYNCHROTRON / Site: APS / Beamline: 19-ID / Wavelength: 0.97918 Å |
| Detector | Type: DECTRIS PILATUS3 X 6M / Detector: PIXEL / Date: Mar 31, 2020 / Details: mirrors |
| Radiation | Monochromator: Si(111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.97918 Å / Relative weight: 1 |
| Reflection | Resolution: 1.35→50 Å / Num. obs: 32168 / % possible obs: 95.7 % / Observed criterion σ(I): -3 / Redundancy: 6.2 % / CC1/2: 0.994 / CC star: 0.998 / Rmerge(I) obs: 0.089 / Net I/σ(I): 24.13 |
| Reflection shell | Resolution: 1.35→1.37 Å / Redundancy: 2.7 % / Rmerge(I) obs: 0.483 / Mean I/σ(I) obs: 2.65 / Num. unique obs: 1515 / CC1/2: 0.747 / CC star: 0.998 / % possible all: 91.4 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 6WCF Resolution: 1.35→36.86 Å / Cor.coef. Fo:Fc: 0.983 / Cor.coef. Fo:Fc free: 0.977 / SU B: 1.434 / SU ML: 0.026 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R: 0.048 / ESU R Free: 0.047 / StereochEM target val spec case: ML Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS U VALUES : REFINED INDIVIDUALLY
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| Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso max: 61.3 Å2 / Biso mean: 13.639 Å2 / Biso min: 6.97 Å2
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| Refinement step | Cycle: final / Resolution: 1.35→36.86 Å
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| Refine LS restraints |
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| LS refinement shell | Resolution: 1.35→1.385 Å / Rfactor Rfree error: 0 / Total num. of bins used: 20
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X-RAY DIFFRACTION
United States, 1items
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