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Yorodumi- PDB-9gwo: SARS-CoV-2 methyltransferase nsp10-16 in complex with SAM and the... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9gwo | ||||||
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| Title | SARS-CoV-2 methyltransferase nsp10-16 in complex with SAM and theophylline derivative LAS 54571126 | ||||||
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Keywords | VIRAL PROTEIN / methyltransferase / complex / inhibitor | ||||||
| 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 / snRNP Assembly / Translation of Replicase and Assembly of the Replication Transcription Complex / Replication of the SARS-CoV-2 genome / Hydrolases; Acting on ester bonds; Exoribonucleases producing 5'-phosphomonoesters / double membrane vesicle viral factory outer membrane / SARS coronavirus main proteinase / host cell endoplasmic reticulum-Golgi intermediate compartment / 5'-3' DNA helicase activity / 3'-5'-RNA exonuclease activity / symbiont-mediated degradation of host mRNA / host cell endosome / mRNA guanylyltransferase / symbiont-mediated suppression of host ISG15-protein conjugation / symbiont-mediated suppression of host toll-like receptor signaling pathway / G-quadruplex RNA binding / symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of IRF3 activity / omega peptidase activity / mRNA (guanine-N7)-methyltransferase / methyltransferase cap1 / SARS-CoV-2 modulates host translation machinery / host cell Golgi apparatus / symbiont-mediated suppression of host NF-kappaB cascade / DNA helicase / symbiont-mediated perturbation of host ubiquitin-like protein modification / 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 / lyase activity / viral protein processing / host cell perinuclear region of cytoplasm / host cell endoplasmic reticulum membrane / RNA helicase / symbiont-mediated suppression of host type I interferon-mediated signaling pathway / copper ion binding / symbiont-mediated suppression of host gene expression / symbiont-mediated activation of host autophagy / viral translational frameshifting / 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: 2 Å | ||||||
Authors | Kremling, V. / Sprenger, J. / Oberthuer, D. / Kiene, A. | ||||||
| Funding support | 1items
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Citation | Journal: To Be PublishedTitle: Crystal structures of SARS-CoV-2 methyltransferase nsp10-16 with Cap0-site binders Authors: Kremling, V. / Sprenger, J. / Oberthuer, D. / Middendorf, P. / Falke, S. / Kiene, A. / Klopprogge, B. / Scheer, T.E.S. / Creon, 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 | 9gwo.cif.gz | 127.8 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9gwo.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 9gwo.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9gwo_validation.pdf.gz | 1.2 MB | Display | wwPDB validaton report |
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| Full document | 9gwo_full_validation.pdf.gz | 1.2 MB | Display | |
| Data in XML | 9gwo_validation.xml.gz | 22 KB | Display | |
| Data in CIF | 9gwo_validation.cif.gz | 28.8 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/gw/9gwo ftp://data.pdbj.org/pub/pdb/validation_reports/gw/9gwo | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9gnyC ![]() 9grpC ![]() 9grqC ![]() 9gs4C ![]() 9gtfC ![]() 9gudC ![]() 9gueC ![]() 9gufC ![]() 9guyC ![]() 9q8hC C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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| 1 |
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| Unit cell |
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Components
-Protein , 2 types, 2 molecules AB
| #1: Protein | Mass: 34150.090 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: rep, 1a-1b / Production host: ![]() |
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| #2: Protein | Mass: 14859.983 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: rep, 1a-1b / Production host: ![]() |
-Non-polymers , 9 types, 133 molecules 














| #3: Chemical | ChemComp-MES / | ||||||||||||||
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| #4: Chemical | ChemComp-EDO / #5: Chemical | #6: Chemical | ChemComp-A1IQS / | Mass: 509.558 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C25H31N7O5 / Feature type: SUBJECT OF INVESTIGATION #7: Chemical | ChemComp-DMS / | #8: Chemical | ChemComp-SAM / | #9: Chemical | #10: Chemical | ChemComp-IMD / | #11: Water | ChemComp-HOH / | |
-Details
| Has ligand of interest | Y |
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| Has protein modification | N |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 4.3 Å3/Da / Density % sol: 71.42 % |
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| Crystal grow | Temperature: 293.15 K / Method: vapor diffusion, hanging drop / pH: 6.5 Details: 400 mM sodium fluoride, 100 mM 2-(N-morpholino)ethanesulfonic acid |
-Data collection
| Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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| Diffraction source | Source: SYNCHROTRON / Site: PETRA III, DESY / Beamline: P11 / Wavelength: 1.03322 Å |
| Detector | Type: DECTRIS EIGER2 X 16M / Detector: PIXEL / Date: Aug 21, 2021 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.03322 Å / Relative weight: 1 |
| Reflection | Resolution: 2→48.74 Å / Num. obs: 56567 / % possible obs: 99.76 % / Redundancy: 11.5 % / Biso Wilson estimate: 36.66 Å2 / CC1/2: 0.998 / CC star: 0.999 / Rmerge(I) obs: 0.1578 / Rpim(I) all: 0.04894 / Rrim(I) all: 0.1653 / Net I/σ(I): 12.85 |
| Reflection shell | Resolution: 2→2.072 Å / Redundancy: 11.7 % / Rmerge(I) obs: 1.88 / Mean I/σ(I) obs: 1.89 / Num. unique obs: 5625 / CC1/2: 0.574 / CC star: 0.854 / Rpim(I) all: 0.5755 / Rrim(I) all: 1.967 / % possible all: 100 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 2→48.74 Å / SU ML: 0.2395 / Cross valid method: FREE R-VALUE / σ(F): 1.56 / Phase error: 20.5305 Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
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| Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL | ||||||||||||||||||||||||
| Displacement parameters | Biso mean: 42.7 Å2 | ||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 2→48.74 Å
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| Refine LS restraints |
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| LS refinement shell | Resolution: 2→2.05 Å
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