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- PDB-6r1i: Structure of porcine Aichi virus polymerase -

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Basic information

Entry
Database: PDB / ID: 6r1i
TitleStructure of porcine Aichi virus polymerase
ComponentsGenome polyprotein
KeywordsTRANSFERASE / virus / RNA / polymerase
Function / homology
Function and homology information


RNA-protein covalent cross-linking / T=pseudo3 icosahedral viral capsid / host cell cytoplasmic vesicle membrane / cytoplasmic vesicle membrane / : / protein complex oligomerization / monoatomic ion channel activity / RNA helicase activity / symbiont entry into host cell / viral RNA genome replication ...RNA-protein covalent cross-linking / T=pseudo3 icosahedral viral capsid / host cell cytoplasmic vesicle membrane / cytoplasmic vesicle membrane / : / protein complex oligomerization / monoatomic ion channel activity / RNA helicase activity / symbiont entry into host cell / viral RNA genome replication / cysteine-type endopeptidase activity / RNA-dependent RNA polymerase activity / DNA-templated transcription / virion attachment to host cell / structural molecule activity / proteolysis / RNA binding / ATP binding
Similarity search - Function
Helicase/polymerase/peptidase polyprotein, Calicivirus-type / Reverse transcriptase/Diguanylate cyclase domain / Picornavirales 3C/3C-like protease domain / Picornavirales 3C/3C-like protease domain profile. / Peptidase C3A/C3B, picornaviral / 3C cysteine protease (picornain 3C) / Picornavirus capsid / picornavirus capsid protein / Helicase, superfamily 3, single-stranded RNA virus / Superfamily 3 helicase of positive ssRNA viruses domain profile. ...Helicase/polymerase/peptidase polyprotein, Calicivirus-type / Reverse transcriptase/Diguanylate cyclase domain / Picornavirales 3C/3C-like protease domain / Picornavirales 3C/3C-like protease domain profile. / Peptidase C3A/C3B, picornaviral / 3C cysteine protease (picornain 3C) / Picornavirus capsid / picornavirus capsid protein / Helicase, superfamily 3, single-stranded RNA virus / Superfamily 3 helicase of positive ssRNA viruses domain profile. / Helicase, superfamily 3, single-stranded DNA/RNA virus / RNA helicase / Picornavirus/Calicivirus coat protein / Viral coat protein subunit / RNA-directed RNA polymerase, C-terminal domain / Viral RNA-dependent RNA polymerase / Reverse transcriptase/Diguanylate cyclase domain / RNA-directed RNA polymerase, catalytic domain / RdRp of positive ssRNA viruses catalytic domain profile. / Alpha-Beta Plaits / Peptidase S1, PA clan, chymotrypsin-like fold / Peptidase S1, PA clan / DNA/RNA polymerase superfamily / P-loop containing nucleoside triphosphate hydrolase / 2-Layer Sandwich / Alpha Beta
Similarity search - Domain/homology
Biological speciesPorcine kobuvirus swine/S-1-HUN/2007/Hungary
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.634 Å
AuthorsDubankova, A. / Boura, E.
Funding support Czech Republic, 1items
OrganizationGrant numberCountry
European Regional Development FundCZ.02.1.01/0.0/0.0/16_019/0000729 Czech Republic
CitationJournal: J.Struct.Biol. / Year: 2019
Title: Structures of kobuviral and siciniviral polymerases reveal conserved mechanism of picornaviral polymerase activation.
Authors: Dubankova, A. / Horova, V. / Klima, M. / Boura, E.
History
DepositionMar 14, 2019Deposition site: PDBE / Processing site: PDBE
Revision 1.0Oct 9, 2019Provider: repository / Type: Initial release
Revision 1.1Nov 6, 2019Group: Data collection / Database references / Category: citation
Item: _citation.journal_volume / _citation.page_first / _citation.page_last
Revision 1.2Jan 24, 2024Group: Data collection / Database references / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Genome polyprotein
B: Genome polyprotein


Theoretical massNumber of molelcules
Total (without water)106,6772
Polymers106,6772
Non-polymers00
Water9,854547
1
A: Genome polyprotein


Theoretical massNumber of molelcules
Total (without water)53,3391
Polymers53,3391
Non-polymers00
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
B: Genome polyprotein


Theoretical massNumber of molelcules
Total (without water)53,3391
Polymers53,3391
Non-polymers00
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)170.448, 170.448, 231.339
Angle α, β, γ (deg.)90.00, 90.00, 120.00
Int Tables number178
Space group name H-MP6122
Components on special symmetry positions
IDModelComponents
11A-556-

HOH

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Components

#1: Protein Genome polyprotein


Mass: 53338.734 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Porcine kobuvirus swine/S-1-HUN/2007/Hungary
Production host: Escherichia coli (E. coli) / References: UniProt: B8R1T8
#2: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 547 / Source method: isolated from a natural source / Formula: H2O

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Experimental details

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Experiment

ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

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Sample preparation

CrystalDensity Matthews: 4.55 Å3/Da / Density % sol: 72.95 %
Crystal growTemperature: 291 K / Method: vapor diffusion, sitting drop
Details: 1.7M (NH4)2SO4, 1.7% (v/v) PEG400, 15% (v/v) glycerol, 85 mM HEPES pH 7.5

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Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: BESSY / Beamline: 14.1 / Wavelength: 0.9184 Å
DetectorType: DECTRIS PILATUS3 6M / Detector: PIXEL / Date: Feb 3, 2018
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9184 Å / Relative weight: 1
ReflectionResolution: 2.634→48.13 Å / Num. obs: 59076 / % possible obs: 99.96 % / Redundancy: 21.9 % / Net I/σ(I): 33.96
Reflection shellResolution: 2.634→2.73 Å / Num. unique obs: 5790

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Processing

Software
NameVersionClassification
PHENIX(1.11.1_2575: ???)refinement
XDSdata reduction
XDSdata scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: polyalanine model based on 4nz0
Resolution: 2.634→48.128 Å / SU ML: 0.26 / Cross valid method: FREE R-VALUE / σ(F): 1.36 / Phase error: 22.39
RfactorNum. reflection% reflection
Rfree0.2219 1137 1.92 %
Rwork0.191 --
obs0.1916 59071 99.98 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å
Refinement stepCycle: LAST / Resolution: 2.634→48.128 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms7496 0 0 547 8043
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0047722
X-RAY DIFFRACTIONf_angle_d0.76410526
X-RAY DIFFRACTIONf_dihedral_angle_d19.6432818
X-RAY DIFFRACTIONf_chiral_restr0.0581138
X-RAY DIFFRACTIONf_plane_restr0.0061366
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.634-2.75390.27711400.23867100X-RAY DIFFRACTION100
2.7539-2.89910.27991390.23857120X-RAY DIFFRACTION100
2.8991-3.08070.25291400.23817142X-RAY DIFFRACTION100
3.0807-3.31850.28011410.22847167X-RAY DIFFRACTION100
3.3185-3.65230.24651410.20437184X-RAY DIFFRACTION100
3.6523-4.18060.18841420.17477247X-RAY DIFFRACTION100
4.1806-5.2660.1881430.15787316X-RAY DIFFRACTION100
5.266-48.13560.20491510.17547658X-RAY DIFFRACTION100

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