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Yorodumi- PDB-7uua: Structure of the SARS-CoV-2 main protease in complex with inhibit... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 7uua | ||||||
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| Title | Structure of the SARS-CoV-2 main protease in complex with inhibitor MPI8 | ||||||
Components | 3C-like proteinase nsp5 | ||||||
Keywords | VIRAL PROTEIN / HYDROLASE/INHIBITOR / main protease / HYDROLASE-INHIBITOR complex | ||||||
| Function / homology | Function and homology informationprotein guanylyltransferase activity / RNA endonuclease activity producing 3'-phosphomonoesters, hydrolytic mechanism / 5'-3' RNA helicase activity / Lyases; Phosphorus-oxygen lyases / mRNA guanylyltransferase activity / 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 / 5'-3' RNA helicase activity / Lyases; Phosphorus-oxygen lyases / mRNA guanylyltransferase activity / 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 / host cell endosome / 3'-5'-RNA exonuclease activity / 5'-3' DNA helicase activity / symbiont-mediated degradation of host mRNA / 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 / symbiont-mediated suppression of host NF-kappaB cascade / host cell Golgi apparatus / DNA helicase / symbiont-mediated perturbation of host ubiquitin-like protein modification / methyltransferase cap1 activity / ubiquitinyl hydrolase 1 / mRNA 5'-cap (guanine-N7-)-methyltransferase activity / cysteine-type deubiquitinase activity / Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases / lyase activity / single-stranded RNA binding / 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 Similarity search - Function | ||||||
| Biological species | ![]() | ||||||
| Method | X-RAY DIFFRACTION / MOLECULAR REPLACEMENT / Resolution: 1.85 Å | ||||||
Authors | Yang, K.S. / Liu, W.R. | ||||||
| Funding support | United States, 1items
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Citation | Journal: Acs Chem.Biol. / Year: 2023Title: A Novel Y-Shaped, S-O-N-O-S-Bridged Cross-Link between Three Residues C22, C44, and K61 Is Frequently Observed in the SARS-CoV-2 Main Protease. Authors: Yang, K.S. / Blankenship, L.R. / Kuo, S.A. / Sheng, Y.J. / Li, P. / Fierke, C.A. / Russell, D.H. / Yan, X. / Xu, S. / Liu, W.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 | 7uua.cif.gz | 96.8 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7uua.ent.gz | 57.9 KB | Display | PDB format |
| PDBx/mmJSON format | 7uua.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/uu/7uua ftp://data.pdbj.org/pub/pdb/validation_reports/uu/7uua | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 7uu6C ![]() 7uu7C ![]() 7uu8C ![]() 7uu9C ![]() 7uubC ![]() 7uucC ![]() 7uudC ![]() 7uueC ![]() 7jpyS S: Starting model for refinement 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
| #1: Protein | Mass: 33873.500 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: rep, 1a-1b / Production host: ![]() References: UniProt: P0DTD1, SARS coronavirus main proteinase |
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| #2: Chemical | ChemComp-NOL / |
| #3: Water | ChemComp-HOH / |
| Has ligand of interest | Y |
| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 2.75 Å3/Da / Density % sol: 55.33 % |
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| Crystal grow | Temperature: 289 K / Method: vapor diffusion, hanging drop / Details: 0.1 M Bis-tris, pH6.5, 16% w/v PEG10k |
-Data collection
| Diffraction | Mean temperature: 120 K / Serial crystal experiment: N |
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| Diffraction source | Source: ROTATING ANODE / Type: RIGAKU MICROMAX-007 HF / Wavelength: 1.54301 Å |
| Detector | Type: Bruker PHOTON II / Detector: PIXEL / Date: Apr 29, 2021 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.54301 Å / Relative weight: 1 |
| Reflection | Resolution: 1.85→24.1 Å / Num. obs: 31339 / % possible obs: 99.9 % / Redundancy: 11.3 % / Biso Wilson estimate: 21.57 Å2 / CC1/2: 0.999 / Net I/σ(I): 13.8 |
| Reflection shell | Resolution: 1.85→1.89 Å / Num. unique obs: 1904 / CC1/2: 0.812 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 7JPY Resolution: 1.85→24.1 Å / SU ML: 0.2774 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 32.6159 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: 28.61 Å2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 1.85→24.1 Å
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| Refine LS restraints |
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| LS refinement shell |
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About Yorodumi




X-RAY DIFFRACTION
United States, 1items
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