SASDG25

DNA repair protein Rad5 (with 6xhis and twin-strep tags)

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2019-12-06T13:07:15.624532+01:00

The simulation code uiowa_BD was used to carry out Langevin dynamics (LD) simulations of Rad5. Two different sets of simulations were carried out in triplicate, with each set using a different starting model of Rad5. The different starting models were generated based on docking results from two different docking servers, ClusPro and ZDOCK. Docking was used to position the HIRAN domain on the helicase domain in an acceptable orientation. For each simulation, a time-step of 125 fs was used, and a snapshot (PDB file) was recorded every ns of simulation time for a total of 5 µs of simulation time. As such, each simulation generated a total of 5000 individual structures. The first set of models displayed in this entry (top) are representatives from the ZDOCK LD simulation while the second set of models (bottom) are representatives derived from ClusPro. A zip file containing the three replicates of each ClusPro and ZDOCK simulation are attached to this entry and made available in the full entry zip archive (5000 PDB files per simulation; ca. 2.2 GB total).

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · DNA repair protein Rad5 (with 6xhis and twin-strep tags)

Concentration— – 7.75 Buffer / pH40 mM Tris, 150 mM KCl, 5 mM DTT, 5% glycerol / 8.0
Experimental temperature20.0 Facility / beamlineAdvanced Photon Source (APS), Argonne National Laboratory / BioCAT 18ID
Wavelength0.1033 nmExposure0.5 s × 19

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
DNA repair protein RAD5
View sequence
>RAD5_HIS_STREP_TAGMHHHHHHSHIEQEERKRFFNDDLDTSETSLNFKSENKESFLFANSHNDDDDDVVVSVSDTTEGEGDRSIVPVRREIEEEGQNQFITELLRIIPEMPKDLVMELNEKFGSQEEGLSLALSHYFDHNSGTSISKIPSSPNQLNTLSDTSNSTLSPSSFHPKRRRIYGFRNQTRLEDKVTWKRFIGALQVTGMATRPTVRPLKYGSQMKLKRSSEEISATKVYDSRGRKKASMASLVRIFDIQYDREIGRVSEDIAQILYPLLSSHEISFEVTLIFCDNKRLSIGDSFILQLDCFLTSLIFEERNDGESLMKRRRTEGGNKREKDNGNFGRTLTETDEELESRSKRLALLKLFDKLRLKPILDEQKALEKHKIELNSDPEIIDLDNDEICSNQVTEVHNNLRDTQHEEETMNLNQLKTFYKAAQSSESLKSLPETEPSRDVFKLELRNYQKQGLTWMLRREQEFAKAASDGEASETGANMINPLWKQFKWPNDMSWAAQNLQQDHVNVEDGIFFYANLHSGEFSLAKPILKTMIKGGILSDEMGLGKTVAAYSLVLSCPHDSDVVDKKLFDIENTAVSDNLPSTWQDNKKPYASKTTLIVVPMSLLTQWSNEFTKANNSPDMYHEVYYGGNVSSLKTLLTKTKTPPTVVLTTYGIVQNEWTKHSKGRMTDEDVNISSGLFSVNFYRIIIDEGHNIRNRTTVTSKAVMALQGKCKWVLTGTPIINRLDDLYSLVKFLELDPWRQINYWKTFVSTPFESKNYKQAFDVVNAILEPVLLRRTKQMKDKDGKPLVELPPKEVVIKRLPFSKSQDLLYKFLLDKAEVSVKSGIARGDLLKKYSTILVHILRLRQVCCHPGLIGSQDENDEDLSKNNKLVTEQTVELDSLMRVVSERFDNSFSKEELDAMIQRLKVKYPDNKSFQSLECSICTTEPMDLDKALFTECGHSFCEKCLFEYIEFQNSKNLGLKCPNCRNQIDACRLLALVQTNSNSKNLEFKPYSPASKSSKITALLKELQLLQDSSAGEQVVIFSQFSTYLDILEKELTHTFSKDVAKIYKFDGRLSLKERTSVLADFAVKDYSRQKILLLSLKAGGVGLNLTCASHAYMMDPWWSPSMEDQAIDRLHRIGQTNSVKVMRFIIQDSIEEKMLRIQEKKRTIGEAMDTDEDERRKRRIEEIQMLFEWSHPQFEKGGGSGGGSGGSAWSHPQFEK
proteinSaccharomyces cerevisiaeP328492–1169monomerMolecule count 1137.693 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11248[3]0.00460116118–0.362719513 1/AHas uncertainty columnMissing 0266sasbdb/entries/25/sasdg25/source/SASDG25.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)17.8—Å
i0Guinier6.043e-052.302e-07—
i0P(r)6.103e-052.32e-07—
mwExperimental140.0—kDa
porod_volumePorod254.0—ų
rgGuinier4.70.03Å
rgP(r)4.920.031Å

These values are reported by SASBDB; SAXSdb did not recalculate them from the experimental curve.

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3. Source Fits and Models Source Fits & Models

Fit 1 · CRYSOL

χ²: 1.2551CorMap p: 0.409692Unit: 1/A

Average of 3 5us simulations using the ZDOCK model

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—dummyOther [static image] ———Model

Fit 2 · CRYSOL

χ²: 1.7366CorMap p: 0.0Unit: 1/A

Average of 3 5us simulations using the ClusPro model.

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—dummyOther [static image] ———Model
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4. Source File Index Source Files

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5. Experiment Description and Publication Experiment & Publication

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6. Complete Source Record Complete Source Record

The following content comes directly from the SASBDB entry. Missing values are shown as “—”; SAXSdb does not infer undeclared units.

Open the original SASBDB entry

Buffer and Sample Properties

Buffer name40 mM Tris, 150 mM KCl, 5 mM DTT, 5% glycerolBuffer concentration—
pH8.0Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2019-03-06Storage / measurement temperature4.0 / 20.0
Exposure time0.5Frames19
Wavelength0.1033Sample-to-detector distance3.5
SourceX-ray synchrotronDetectorPilatus3 X 1M
Facility / beamlineAdvanced Photon Source (APS), Argonne National Laboratory / BioCAT 18ID · Lemont, IL, USA
q range0.046 – 3.627Sample volume / flow rate175.0 / 0.7

Original SASBDB Plots

Experimental I(q)
Experimental I(q)
Experimental I(q), log-log
Experimental I(q), log-log
Guinier plot
Guinier plot
Kratky plot
Kratky plot
P(r) plot
P(r) plot

Downloadable Files

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All source fields (unfiltered)

Every source field is expanded here, including empty values, list members and fields already shown above.

summary.json:179 field values
Field pathRaw value
codeSASDG25
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleConformational flexibility of fork-remodeling helicase Rad5 shown by full-ensemble hybrid methods.
project.publication.titleConformational flexibility of fork-remodeling helicase Rad5 shown by full-ensemble hybrid methods.
project.publication.author_listGildenberg MS, Washington MT
project.publication.journalPLoS One
project.publication.doi10.1371/journal.pone.0223875
project.publication.pmid31626633
project.publication.published_date2019
project.statusreleased
project.submitted_date2019-08-29
project.released_date2019-10-08
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDG25.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDG25.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDG25_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDG25_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDG25_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDG25_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDG25.sascif
experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus3 X 1M
experiment.instrument.detector.resolution0.172
experiment.instrument.nameAdvanced Photon Source (APS), Argonne National Laboratory
experiment.instrument.cityLemont, IL
experiment.instrument.countryUSA
experiment.instrument.beamline_nameBioCAT 18ID
experiment.instrument.beam_geometrynull
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
experiment.instrument.line_collimationnull
experiment.instrument.sample_path_lengthnull
experiment.instrument.line_collimation_slitlengthnull
experiment.instrument.line_collimation_integrationwidthnull
experiment.instrument.xray_energynull
experiment.instrument.beam_profile_ahnull
experiment.instrument.beam_profile_alnull
experiment.sample.molecule[0].long_nameDNA repair protein RAD5
experiment.sample.molecule[0].short_nameRad5
experiment.sample.molecule[0].sequence>Rad5_his_strep_tag MHHHHHHSHIEQEERKRFFNDDLDTSETSLNFKSENKESFLFANSHNDDDDDVVVSVSDTTEGEGDRSIVPVRREIEEEGQNQFITELLRIIPEMPKDLVMELNEKFGSQEEGLSLALSHYFDHNSGTSISKIPSSPNQLNTLSDTSNSTLSPSSFHPKRRRIYGFRNQTRLEDKVTWKRFIGALQVTGMATRPTVRPLKYGSQMKLKRSSEEISATKVYDSRGRKKASMASLVRIFDIQYDREIGRVSEDIAQILYPLLSSHEISFEVTLIFCDNKRLSIGDSFILQLDCFLTSLIFEERNDGESLMKRRRTEGGNKREKDNGNFGRTLTETDEELESRSKRLALLKLFDKLRLKPILDEQKALEKHKIELNSDPEIIDLDNDEICSNQVTEVHNNLRDTQHEEETMNLNQLKTFYKAAQSSESLKSLPETEPSRDVFKLELRNYQKQGLTWMLRREQEFAKAASDGEASETGANMINPLWKQFKWPNDMSWAAQNLQQDHVNVEDGIFFYANLHSGEFSLAKPILKTMIKGGILSDEMGLGKTVAAYSLVLSCPHDSDVVDKKLFDIENTAVSDNLPSTWQDNKKPYASKTTLIVVPMSLLTQWSNEFTKANNSPDMYHEVYYGGNVSSLKTLLTKTKTPPTVVLTTYGIVQNEWTKHSKGRMTDEDVNISSGLFSVNFYRIIIDEGHNIRNRTTVTSKAVMALQGKCKWVLTGTPIINRLDDLYSLVKFLELDPWRQINYWKTFVSTPFESKNYKQAFDVVNAILEPVLLRRTKQMKDKDGKPLVELPPKEVVIKRLPFSKSQDLLYKFLLDKAEVSVKSGIARGDLLKKYSTILVHILRLRQVCCHPGLIGSQDENDEDLSKNNKLVTEQTVELDSLMRVVSERFDNSFSKEELDAMIQRLKVKYPDNKSFQSLECSICTTEPMDLDKALFTECGHSFCEKCLFEYIEFQNSKNLGLKCPNCRNQIDACRLLALVQTNSNSKNLEFKPYSPASKSSKITALLKELQLLQDSSAGEQVVIFSQFSTYLDILEKELTHTFSKDVAKIYKFDGRLSLKERTSVLADFAVKDYSRQKILLLSLKAGGVGLNLTCASHAYMMDPWWSPSMEDQAIDRLHRIGQTNSVKVMRFIIQDSIEEKMLRIQEKKRTIGEAMDTDEDERRKRRIEEIQMLFEWSHPQFEKGGGSGGGSGGSAWSHPQFEK
experiment.sample.molecule[0].organismSaccharomyces cerevisiae
experiment.sample.molecule[0].uniprot_codeP32849
experiment.sample.molecule[0].uniprot_range_first2
experiment.sample.molecule[0].uniprot_range_last1169
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMSHIEQEERKRFFNDDLDTSETSLNFKSENKESFLFANSHNDDDDDVVVSVSDTTEGEGD RSIVPVRREIEEEGQNQFITELLRIIPEMPKDLVMELNEKFGSQEEGLSLALSHYFDHNS GTSISKIPSSPNQLNTLSDTSNSTLSPSSFHPKRRRIYGFRNQTRLEDKVTWKRFIGALQ VTGMATRPTVRPLKYGSQMKLKRSSEEISATKVYDSRGRKKASMASLVRIFDIQYDREIG RVSEDIAQILYPLLSSHEISFEVTLIFCDNKRLSIGDSFILQLDCFLTSLIFEERNDGES LMKRRRTEGGNKREKDNGNFGRTLTETDEELESRSKRLALLKLFDKLRLKPILDEQKALE KHKIELNSDPEIIDLDNDEICSNQVTEVHNNLRDTQHEEETMNLNQLKTFYKAAQSSESL KSLPETEPSRDVFKLELRNYQKQGLTWMLRREQEFAKAASDGEASETGANMINPLWKQFK WPNDMSWAAQNLQQDHVNVEDGIFFYANLHSGEFSLAKPILKTMIKGGILSDEMGLGKTV AAYSLVLSCPHDSDVVDKKLFDIENTAVSDNLPSTWQDNKKPYASKTTLIVVPMSLLTQW SNEFTKANNSPDMYHEVYYGGNVSSLKTLLTKTKTPPTVVLTTYGIVQNEWTKHSKGRMT DEDVNISSGLFSVNFYRIIIDEGHNIRNRTTVTSKAVMALQGKCKWVLTGTPIINRLDDL YSLVKFLELDPWRQINYWKTFVSTPFESKNYKQAFDVVNAILEPVLLRRTKQMKDKDGKP LVELPPKEVVIKRLPFSKSQDLLYKFLLDKAEVSVKSGIARGDLLKKYSTILVHILRLRQ VCCHPGLIGSQDENDEDLSKNNKLVTEQTVELDSLMRVVSERFDNSFSKEELDAMIQRLK VKYPDNKSFQSLECSICTTEPMDLDKALFTECGHSFCEKCLFEYIEFQNSKNLGLKCPNC RNQIDACRLLALVQTNSNSKNLEFKPYSPASKSSKITALLKELQLLQDSSAGEQVVIFSQ FSTYLDILEKELTHTFSKDVAKIYKFDGRLSLKERTSVLADFAVKDYSRQKILLLSLKAG GVGLNLTCASHAYMMDPWWSPSMEDQAIDRLHRIGQTNSVKVMRFIIQDSIEEKMLRIQE KKRTIGEAMDTDEDERRKRRIEEIQMLFE
experiment.sample.molecule[0].mw137.693
experiment.sample.molecule[0].total_mw137.693
experiment.sample.molecule[0].number_molecules1
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionnull
experiment.sample.buffer.name40 mM Tris, 150 mM KCl, 5 mM DTT, 5% glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph8.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameDNA repair protein Rad5 (with 6xhis and twin-strep tags)
experiment.sample.ext_coefficientnull
experiment.sample.contrastnull
experiment.sample.specific_volnull
experiment.sample.dry_volnull
experiment.sample.absorbptionnull
experiment.sample.deuterationnull
experiment.sample.mixturenull
experiment.contributor[0].affiliation[0].short_namenull
experiment.contributor[0].affiliation[0].addressIowa, USA
experiment.contributor[0].affiliation[0].full_nameUniversity of Iowa Carver College of Medicine
experiment.contributor[0].affiliation[0].webpagehttps://medicine.uiowa.edu/
experiment.contributor[0].contributor_nameMelissa
experiment.contributor[0].contributor_surnameGildenberg
experiment.contributor[0].orcid
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2019-03-06
experiment.storage_temperature4.0
experiment.cell_temperature20.0
experiment.exposure_time0.5
experiment.number_of_frames19
experiment.wavelength0.1033
experiment.sample_detector_distance3.5
experiment.concentration_minnull
experiment.concentration_max7.75
experiment.sample_volume175.0
experiment.flow_rate0.7
experiment.s_min0.046
experiment.s_max3.627
experiment.total_exposure_timenull
experiment.seccolumn1
fits[0].models[0].model_plotnull
fits[0].models[0].softwareOther [static image]
fits[0].models[0].pdb_link[]
fits[0].models[0].model_titlenull
fits[0].models[0].type_of_modeldummy
fits[0].models[0].software_versionnull
fits[0].models[0].model_datahttps://www.sasbdb.org/media/pdb_file/SASDG25_fit1_model1.png
fits[0].models[0].model_mwnull
fits[0].models[0].bead_radiusnull
fits[0].models[0].lognull
fits[0].models[0].symmetrynull
fits[0].models[0].commentnull
fits[0].models[0].user478
fits[0].fit_unit1/A
fits[0].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/zdock_avg_fixed_fit_img.png
fits[0].softwareCRYSOL
fits[0].chi_square_value1.2551
fits[0].p_value0.409692
fits[0].fit_residual_plotzdock_avg_fitresiduals_img.png
fits[0].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDG25_fit1.fit
fits[0].fit_lognull
fits[0].software_versionnull
fits[0].descriptionAverage of 3 5us simulations using the ZDOCK model
fits[1].models[0].model_plotnull
fits[1].models[0].softwareOther [static image]
fits[1].models[0].pdb_link[]
fits[1].models[0].model_titlenull
fits[1].models[0].type_of_modeldummy
fits[1].models[0].software_versionnull
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fits[1].models[0].model_mwnull
fits[1].models[0].bead_radiusnull
fits[1].models[0].lognull
fits[1].models[0].symmetrynull
fits[1].models[0].commentnull
fits[1].models[0].user478
fits[1].fit_unit1/A
fits[1].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/cluspro_avg_fixed_fit_img.png
fits[1].softwareCRYSOL
fits[1].chi_square_value1.7366
fits[1].p_value0.0
fits[1].fit_residual_plotcluspro_avg_fitresiduals_img.png
fits[1].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDG25_fit2.fit
fits[1].fit_lognull
fits[1].software_versionnull
fits[1].descriptionAverage of 3 5us simulations using the ClusPro model.
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionThe simulation code uiowa_BD was used to carry out Langevin dynamics (LD) simulations of Rad5. Two different sets of simulations were carried out in triplicate, with each set using a different starting model of Rad5. The different starting models were generated based on docking results from two different docking servers, ClusPro and ZDOCK. Docking was used to position the HIRAN domain on the helicase domain in an acceptable orientation. For each simulation, a time-step of 125 fs was used, and a snapshot (PDB file) was recorded every ns of simulation time for a total of 5 µs of simulation time. As such, each simulation generated a total of 5000 individual structures. The first set of models displayed in this entry (top) are representatives from the ZDOCK LD simulation while the second set of models (bottom) are representatives derived from ClusPro. A zip file containing the three replicates of each ClusPro and ZDOCK simulation are attached to this entry and made available in the full entry zip archive (5000 PDB files per simulation; ca. 2.2 GB total).
experiment_descriptionSynchrotron SAXS data from solutions of DNA repair protein Rad5 in 40 mM Tris, 150 mM KCl, 5 mM DTT, 5% glycerol, pH 8 were collected on the BioCAT 18ID beam line at the Advanced Photon Source (APS) Argonne National Laboratory (Lemont, IL, USA) using a Pilatus3 X 1M detector at a sample-detector distance of 3.5 m and at a wavelength of λ = 0.1033 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 175.00 μl sample at 7.8 mg/ml was injected at a 0.70 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 20°C. 19 successive 0.500 second frames were collected through the SEC elution peak of the sample. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[]
intensity_unitnull
experimental_mw140.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i06.103e-05
pddf_i0_error2.32e-07
guinier_i06.043e-05
guinier_i0_error2.302e-07
pddf_rg4.92
pddf_rg_error0.031
guinier_rg4.7
guinier_rg_error0.03
pddf_dmax17.8
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manifest.json:36 field values
Field pathRaw value
codeSASDG25
statussuccess
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View the complete summary.json source
{
  "code": "SASDG25",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "Conformational flexibility of fork-remodeling helicase Rad5 shown by full-ensemble hybrid methods.",
    "publication": {
      "title": "Conformational flexibility of fork-remodeling helicase Rad5 shown by full-ensemble hybrid methods.",
      "author_list": "Gildenberg MS, Washington MT",
      "journal": "PLoS One",
      "doi": "10.1371/journal.pone.0223875",
      "pmid": "31626633",
      "published_date": "2019"
    },
    "status": "released",
    "submitted_date": "2019-08-29",
    "released_date": "2019-10-08"
  },
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  "intensities_kratky_plot": "https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDG25_kratky_img.png",
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      "city": "Lemont, IL",
      "country": "USA",
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          "long_name": "DNA repair protein RAD5",
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          "uniprot_range_last": 1169,
          "oligomerization": "monomer",
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View the complete manifest.json source
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