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Yorodumi- PDB-6men: Crystal structure of a Tylonycteris bat coronavirus HKU4 macrodom... -
+Open data
-Basic information
Entry | Database: PDB / ID: 6men | ||||||
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Title | Crystal structure of a Tylonycteris bat coronavirus HKU4 macrodomain in complex with adenosine diphosphate glucose (ADP-glucose) | ||||||
Components | Replicase polyprotein 1ab | ||||||
Keywords | HYDROLASE / Coronavirus / macrodomain / ADP-ribose / ADP-ribosylhydrolase | ||||||
Function / homology | Function and homology information host cell membrane / Lyases; Phosphorus-oxygen lyases / Hydrolases; Acting on ester bonds; Exoribonucleases producing 5'-phosphomonoesters / host cell endoplasmic reticulum-Golgi intermediate compartment / 3'-5'-RNA exonuclease activity / 5'-3' DNA helicase activity / symbiont-mediated suppression of host NF-kappaB cascade / symbiont-mediated degradation of host mRNA / mRNA guanylyltransferase / symbiont-mediated suppression of host ISG15-protein conjugation ...host cell membrane / Lyases; Phosphorus-oxygen lyases / Hydrolases; Acting on ester bonds; Exoribonucleases producing 5'-phosphomonoesters / host cell endoplasmic reticulum-Golgi intermediate compartment / 3'-5'-RNA exonuclease activity / 5'-3' DNA helicase activity / symbiont-mediated suppression of host NF-kappaB cascade / symbiont-mediated degradation of host mRNA / mRNA guanylyltransferase / symbiont-mediated suppression of host ISG15-protein conjugation / G-quadruplex RNA binding / mRNA (guanine-N7)-methyltransferase / omega peptidase activity / methyltransferase cap1 / symbiont-mediated perturbation of host ubiquitin-like protein modification / endonuclease activity / DNA helicase / mRNA (nucleoside-2'-O-)-methyltransferase activity / mRNA 5'-cap (guanine-N7-)-methyltransferase activity / ubiquitinyl hydrolase 1 / cysteine-type deubiquitinase activity / Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases / RNA helicase activity / host cell perinuclear region of cytoplasm / single-stranded RNA binding / viral protein processing / lyase activity / RNA helicase / symbiont-mediated suppression of host type I interferon-mediated signaling pathway / induction by virus of host autophagy / RNA-directed RNA polymerase / viral translational frameshifting / viral RNA genome replication / cysteine-type endopeptidase activity / RNA-dependent RNA polymerase activity / virus-mediated perturbation of host defense response / DNA-templated transcription / ATP hydrolysis activity / proteolysis / zinc ion binding / ATP binding / membrane Similarity search - Function | ||||||
Biological species | Bat coronavirus HKU4 | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.5 Å | ||||||
Authors | Hammond, R.G. / Schormann, N. / McPherson, R.L. / Leung, A.K.L. / Deivanayagam, C.C.S. / Johnson, M.A. | ||||||
Funding support | United States, 1items
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Citation | Journal: Proc.Natl.Acad.Sci.USA / Year: 2021 Title: ADP-Ribose and Analogues bound to the DeMARylating Macrodomain from the Bat Coronavirus HKU4 Authors: Hammond, R.G. / Schormann, N. / McPherson, R.L. / Leung, A.K.L. / Deivanayagam, C. / Johnson, M.A. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 6men.cif.gz | 141 KB | Display | PDBx/mmCIF format |
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PDB format | pdb6men.ent.gz | 109.4 KB | Display | PDB format |
PDBx/mmJSON format | 6men.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 6men_validation.pdf.gz | 1.1 MB | Display | wwPDB validaton report |
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Full document | 6men_full_validation.pdf.gz | 1.1 MB | Display | |
Data in XML | 6men_validation.xml.gz | 17.8 KB | Display | |
Data in CIF | 6men_validation.cif.gz | 24.6 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/me/6men ftp://data.pdbj.org/pub/pdb/validation_reports/me/6men | HTTPS FTP |
-Related structure data
Related structure data | 6meaSC 6mebC S: Starting model for refinement C: citing same article (ref.) |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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2 |
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Unit cell |
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-Components
#1: Protein | Mass: 18595.129 Da / Num. of mol.: 2 / Fragment: macrodomain (UNP residues 1154-1324) Source method: isolated from a genetically manipulated source Source: (gene. exp.) Bat coronavirus HKU4 / Gene: rep, 1a-1b / Plasmid: pET15b-TEV / Cell line (production host): BL21(DE3)pLysS / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: P0C6W3 #2: Chemical | #3: Water | ChemComp-HOH / | |
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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: 2.3 Å3/Da / Density % sol: 46.58 % |
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Crystal grow | Temperature: 295 K / Method: vapor diffusion, hanging drop Details: 20-25% PEG3350, 0.1 M HEPES, pH 7.0-7.5, protein:ligand molar ratio 1:10 PH range: 7.0-7.5 |
-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: SYNCHROTRON / Site: APS / Beamline: 22-ID / Wavelength: 1 Å |
Detector | Type: RAYONIX MX300-HS / Detector: CCD / Date: Jul 2, 2017 / Details: Mirrors |
Radiation | Monochromator: double crystal Si(111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
Reflection | Resolution: 1.5→39.86 Å / Num. obs: 49739 / % possible obs: 99.9 % / Redundancy: 7.5 % / Biso Wilson estimate: 16.1 Å2 / CC1/2: 0.995 / Rmerge(I) obs: 0.129 / Rpim(I) all: 0.051 / Rrim(I) all: 0.139 / Net I/σ(I): 9.1 / Num. measured all: 371270 / Scaling rejects: 23 |
Reflection shell | Resolution: 1.5→1.53 Å / Redundancy: 7.4 % / Rmerge(I) obs: 1.284 / Mean I/σ(I) obs: 1.9 / Num. unique obs: 2476 / CC1/2: 0.721 / Rpim(I) all: 0.508 / Rrim(I) all: 1.382 / % possible all: 100 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: PDB entry 6MEA Resolution: 1.5→29.21 Å / Cor.coef. Fo:Fc: 0.965 / Cor.coef. Fo:Fc free: 0.953 / SU B: 3.424 / SU ML: 0.06 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R: 0.089 / ESU R Free: 0.077 Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS U VALUES : REFINED INDIVIDUALLY
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Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso max: 71.15 Å2 / Biso mean: 24.8 Å2 / Biso min: 8.73 Å2
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Refinement step | Cycle: final / Resolution: 1.5→29.21 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 1.5→1.539 Å / Rfactor Rfree error: 0 / Total num. of bins used: 20
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