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Yorodumi- PDB-8rv4: SARS-CoV-2 nsp16-nsp10 in complex with SAM derivative inhibitor 2 -
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Open data
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Basic information
| Entry | Database: PDB / ID: 8rv4 | ||||||
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| Title | SARS-CoV-2 nsp16-nsp10 in complex with SAM derivative inhibitor 2 | ||||||
Components |
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Keywords | VIRAL PROTEIN / nsp16 / nsp10 / 2'-O-methyltransferase | ||||||
| Function / homology | Function and homology informationviral genome replication / methyltransferase 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 ...viral genome replication / methyltransferase 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 / endonuclease 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 / methylation / 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: 2.35 Å | ||||||
Authors | Kalnins, G. | ||||||
| Funding support | 1items
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Citation | Journal: Chemmedchem / Year: 2024Title: Structural Basis for Inhibition of the SARS-CoV-2 nsp16 by Substrate-Based Dual Site Inhibitors. Authors: Kalnins, G. / Rudusa, L. / Bula, A.L. / Zelencova-Gopejenko, D. / Bobileva, O. / Sisovs, M. / Tars, K. / Jirgensons, A. / Jaudzems, K. / Bobrovs, R. | ||||||
| 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 | 8rv4.cif.gz | 120.3 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8rv4.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 8rv4.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 8rv4_validation.pdf.gz | 728.9 KB | Display | wwPDB validaton report |
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| Full document | 8rv4_full_validation.pdf.gz | 732.6 KB | Display | |
| Data in XML | 8rv4_validation.xml.gz | 18 KB | Display | |
| Data in CIF | 8rv4_validation.cif.gz | 24.7 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/rv/8rv4 ftp://data.pdbj.org/pub/pdb/validation_reports/rv/8rv4 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 8rv5C ![]() 8rv6C ![]() 8rv7C ![]() 8rv8C ![]() 8rv9C ![]() 8rvaC ![]() 8rvbC ![]() 8rzcC ![]() 8rzdC ![]() 8rzeC 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: 33701.645 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: 15078.259 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Production host: ![]() |
-Non-polymers , 4 types, 89 molecules 




| #3: Chemical | ChemComp-MES / | ||
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| #4: Chemical | ChemComp-A1H3C / Mass: 493.535 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C24H23N5O5S / Feature type: SUBJECT OF INVESTIGATION | ||
| #5: Chemical | | #6: 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: 4.27 Å3/Da / Density % sol: 71.18 % |
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| Crystal grow | Temperature: 293 K / Method: vapor diffusion, sitting drop / pH: 5.6 Details: 0.1 M MES (pH 5.6), 5% PEG 3350, 0.24 M magnesium chloride |
-Data collection
| Diffraction | Mean temperature: 90 K / Serial crystal experiment: N |
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| Diffraction source | Source: SYNCHROTRON / Site: Diamond / Beamline: I03 / Wavelength: 0.97624 Å |
| Detector | Type: DECTRIS EIGER2 XE 16M / Detector: PIXEL / Date: Aug 4, 2023 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.97624 Å / Relative weight: 1 |
| Reflection | Resolution: 2.35→84.27 Å / Num. obs: 35621 / % possible obs: 100 % / Redundancy: 20.8 % / Biso Wilson estimate: 53.09 Å2 / CC1/2: 0.999 / Rmerge(I) obs: 0.184 / Rpim(I) all: 0.041 / Rrim(I) all: 0.189 / Χ2: 0.97 / Net I/σ(I): 12.1 |
| Reflection shell | Resolution: 2.35→2.43 Å / Redundancy: 21.4 % / Rmerge(I) obs: 2.34 / Mean I/σ(I) obs: 1.8 / Num. unique obs: 73623 / CC1/2: 0.699 / Rpim(I) all: 0.514 / Rrim(I) all: 2.396 / Χ2: 0.92 / % possible all: 100 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.35→72.98 Å / SU ML: 0.3088 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 25.9543 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: 53.09 Å2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 2.35→72.98 Å
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| Refine LS restraints |
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| LS refinement shell |
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