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Yorodumi- PDB-8ov4: SARS-CoV-2 nsp10-16 methyltransferase in complex with Toyocamycin -
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Open data
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Basic information
| Entry | Database: PDB / ID: 8ov4 | ||||||
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| Title | SARS-CoV-2 nsp10-16 methyltransferase in complex with Toyocamycin | ||||||
 Components | 
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 Keywords | VIRAL PROTEIN / methyltransferase / complex / inhibitor / SARS-CoV-2 | ||||||
| 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: 1.93 Å  | ||||||
 Authors | Kremling, V. / Sprenger, J. / Oberthuer, D. | ||||||
| Funding support | 1items 
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 Citation |  Journal: Elife / Year: 2024Title: SARS-CoV-2 methyltransferase nsp10-16 in complex with natural and drug-like purine analogs for guiding structure-based drug discovery Authors: Kremling, V. / Falke, S. / Fernandez-Garcia, Y. / Ehrt, C. / Kiene, A. / Klopprogge, B. / Scheer, E. / Barthels, F. / Middendorf, P. / Kuhn, S. / Gunther, S. / Rarey, M. / Chapman, H.N. / ...Authors: Kremling, V. / Falke, S. / Fernandez-Garcia, Y. / Ehrt, C. / Kiene, A. / Klopprogge, B. / Scheer, E. / Barthels, F. / Middendorf, P. / Kuhn, S. / Gunther, S. / Rarey, M. / Chapman, H.N. / Oberthur, D. / Sprenger, J.  | ||||||
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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 |  8ov4.cif.gz | 218.7 KB | Display |  PDBx/mmCIF format | 
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| PDB format |  pdb8ov4.ent.gz | 141.8 KB | Display |  PDB format | 
| PDBx/mmJSON format |  8ov4.json.gz | Tree view |  PDBx/mmJSON format | |
| Others |  Other downloads | 
-Validation report
| Summary document |  8ov4_validation.pdf.gz | 812.5 KB | Display |  wwPDB validaton report | 
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| Full document |  8ov4_full_validation.pdf.gz | 819.3 KB | Display | |
| Data in XML |  8ov4_validation.xml.gz | 21.1 KB | Display | |
| Data in CIF |  8ov4_validation.cif.gz | 29.9 KB | Display | |
| Arichive directory |  https://data.pdbj.org/pub/pdb/validation_reports/ov/8ov4 ftp://data.pdbj.org/pub/pdb/validation_reports/ov/8ov4 | HTTPS FTP  | 
-Related structure data
| Related structure data | ![]() 8bsdC ![]() 8bzvC ![]() 8c5mC ![]() 8osxC ![]() 8ot0C ![]() 8otoC ![]() 8otrC ![]() 8ov1C ![]() 8ov2C ![]() 8ov3C ![]() 8s8wC ![]() 8s8xC ![]() 9emlC ![]() 9emvC 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 on special symmetry positions | 
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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 , 5 types, 264 molecules 








| #3: Chemical | ChemComp-EDO / #4: Chemical |  ChemComp-MES /  | #5: Chemical |  ChemComp-TO1 /  | #6: Chemical | #7: Water |  ChemComp-HOH /  |  | 
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-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 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  | 
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-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: Feb 22, 2023 | 
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | 
| Radiation wavelength | Wavelength: 1.0332 Å / Relative weight: 1 | 
| Reflection | Resolution: 1.93→48.73 Å / Num. obs: 62937 / % possible obs: 99.9 % / Redundancy: 8.1 % / Biso Wilson estimate: 38.46 Å2 / CC1/2: 0.997 / CC star: 0.999 / Rmerge(I) obs: 0.1371 / Rpim(I) all: 0.05097 / Rrim(I) all: 0.1465 / Net I/σ(I): 9.1 | 
| Reflection shell | Resolution: 1.93→1.999 Å / Redundancy: 8.3 % / Rmerge(I) obs: 1.973 / Mean I/σ(I) obs: 0.8 / Num. unique obs: 6239 / CC1/2: 0.398 / CC star: 0.755 / Rpim(I) all: 0.7243 / Rrim(I) all: 2.104 / % possible all: 100 | 
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Processing
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| Refinement | Method to determine structure:  MOLECULAR REPLACEMENT / Resolution: 1.93→48.73 Å / SU ML: 0.2427  / Cross valid method: FREE R-VALUE / σ(F): 1.35  / Phase error: 24.5168 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: 47.81 Å2 | ||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 1.93→48.73 Å
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| Refine LS restraints | 
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| LS refinement shell | 
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X-RAY DIFFRACTION
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