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Yorodumi- PDB-9grq: 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: 9grq | ||||||
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| Title | SARS-CoV-2 methyltransferase nsp10-16 in complex with SAM and theophylline | ||||||
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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 / 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 / viral protein processing / host cell perinuclear region of cytoplasm / 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: 1.85 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. / Chapman, H.N. / Middendorf, P. / Falke, S. / Kiene, A. / Klopprogge, B. / Scheer, T.E.S. / Creon, A. | ||||||
| History |
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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 | 9grq.cif.gz | 247.3 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9grq.ent.gz | 162.8 KB | Display | PDB format |
| PDBx/mmJSON format | 9grq.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9grq_validation.pdf.gz | 1.2 MB | Display | wwPDB validaton report |
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| Full document | 9grq_full_validation.pdf.gz | 1.2 MB | Display | |
| Data in XML | 9grq_validation.xml.gz | 26 KB | Display | |
| Data in CIF | 9grq_validation.cif.gz | 35.4 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/gr/9grq ftp://data.pdbj.org/pub/pdb/validation_reports/gr/9grq | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9gnyC ![]() 9grpC ![]() 9gs4C ![]() 9gtfC ![]() 9gudC ![]() 9gueC ![]() 9gufC ![]() 9guyC ![]() 9gwoC ![]() 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 , 7 types, 371 molecules 












| #3: Chemical | ChemComp-TEP / | ||||||||||
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| #4: Chemical | ChemComp-EDO / #5: Chemical | #6: Chemical | #7: Chemical | ChemComp-SAM / | #8: Chemical | #9: Water | ChemComp-HOH / | |
-Details
| Has ligand of interest | Y |
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-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 4.21 Å3/Da / Density % sol: 70.8 % |
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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: 1.0332 Å |
| Detector | Type: DECTRIS EIGER2 X 16M / Detector: PIXEL / Date: Aug 20, 2021 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.0332 Å / Relative weight: 1 |
| Reflection | Resolution: 1.85→48.1 Å / Num. obs: 69991 / % possible obs: 99.98 % / Redundancy: 8.7 % / Biso Wilson estimate: 29.71 Å2 / CC1/2: 0.997 / CC star: 0.999 / Rmerge(I) obs: 0.1597 / Rpim(I) all: 0.05704 / Rrim(I) all: 0.1698 / Net I/σ(I): 9.16 |
| Reflection shell | Resolution: 1.85→1.916 Å / Redundancy: 8.9 % / Rmerge(I) obs: 1.763 / Num. unique obs: 6979 / CC1/2: 0.442 / CC star: 0.783 / Rpim(I) all: 0.6186 / Rrim(I) all: 1.87 / % possible all: 100 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.85→48.1 Å / SU ML: 0.2264 / Cross valid method: FREE R-VALUE / σ(F): 1.85 / Phase error: 22.8969 Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
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| Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.1 Å / Solvent model: FLAT BULK SOLVENT MODEL | ||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 38.59 Å2 | ||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 1.85→48.1 Å
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| Refine LS restraints |
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| LS refinement shell | Resolution: 1.85→1.916 Å
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| Refinement TLS params. | Method: refined / Origin x: 82.915073072 Å / Origin y: -21.6828885553 Å / Origin z: -5.78325155214 Å
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| Refinement TLS group | Selection details: all |
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