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Yorodumi- PDB-9eun: SARS-CoV-2 nsp10-16 methyltransferase in complex with SAM and m7GTP -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9eun | ||||||
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| Title | SARS-CoV-2 nsp10-16 methyltransferase in complex with SAM and m7GTP | ||||||
Components |
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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: 2.33 Å | ||||||
Authors | Kremling, V. / Sprenger, J. / Oberthuer, D. / Scheer, T.E.S. | ||||||
| Funding support | Germany, 1items
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Citation | Journal: To Be PublishedTitle: SARS-CoV-2 methyltransferase nsp10-16 in complex with natural and drug-like purine analogs for guiding structure-based drug development Authors: Kremling, V. / Falke, S. / Fernandez-Garcia, Y. / Ehrt, C. / Kiene, A. / Klopprogge, B. / Scheer, T.E.S. / Barthels, F. / Middendorf, P. / Kuehn, S. / Guenther, S. / Rarey, M. / Chapman, H.N. ...Authors: Kremling, V. / Falke, S. / Fernandez-Garcia, Y. / Ehrt, C. / Kiene, A. / Klopprogge, B. / Scheer, T.E.S. / Barthels, F. / Middendorf, P. / Kuehn, S. / Guenther, S. / Rarey, M. / Chapman, H.N. / Oberthuer, D. / Sprenger, J. | ||||||
| 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 | 9eun.cif.gz | 213 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9eun.ent.gz | 137.4 KB | Display | PDB format |
| PDBx/mmJSON format | 9eun.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9eun_validation.pdf.gz | 1.1 MB | Display | wwPDB validaton report |
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| Full document | 9eun_full_validation.pdf.gz | 1.1 MB | Display | |
| Data in XML | 9eun_validation.xml.gz | 20.3 KB | Display | |
| Data in CIF | 9eun_validation.cif.gz | 28.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/eu/9eun ftp://data.pdbj.org/pub/pdb/validation_reports/eu/9eun | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9emjC 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 , 6 types, 202 molecules 










| #3: Chemical | ChemComp-MES / | ||||
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| #4: Chemical | ChemComp-SAM / | ||||
| #5: Chemical | ChemComp-MGP / | ||||
| #6: Chemical | ChemComp-EDO / #7: Chemical | #8: 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: 4.3 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 EIGER X 16M / Detector: PIXEL / Date: Dec 7, 2023 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.03322 Å / Relative weight: 1 |
| Reflection | Resolution: 2.33→48.99 Å / Num. obs: 69857 / % possible obs: 99.89 % / Redundancy: 12 % / Biso Wilson estimate: 48.47 Å2 / CC1/2: 0.989 / CC star: 0.997 / Rmerge(I) obs: 0.4043 / Rpim(I) all: 0.1213 / Rrim(I) all: 0.4223 / Net I/σ(I): 4.62 |
| Reflection shell | Resolution: 2.33→2.39 Å / Redundancy: 11 % / Rmerge(I) obs: 3.338 / Mean I/σ(I) obs: 0.35 / Num. unique obs: 5368 / CC1/2: 0.202 / CC star: 0.579 / Rpim(I) all: 1.046 / Rrim(I) all: 3.5 / % possible all: 99.93 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.33→48.99 Å / SU ML: 0.3335 / Cross valid method: FREE R-VALUE / σ(F): 1.35 / Phase error: 24.3943 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: 52.09 Å2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 2.33→48.99 Å
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| Refine LS restraints |
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| LS refinement shell |
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X-RAY DIFFRACTION
Germany, 1items
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