SASDW97

Recombination directionality factor (6H-RdfS) from M.japonicum bound to 40mer DNA

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2025-04-02T23:34:23.155761+02:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Recombination directionality factor (6H-RdfS) from M.japonicum bound to 40mer DNA

Concentration— – 6.8 Buffer / pH150 mM Tris-HCl, 300 mM NaCl, 5% v/v glycerol / 7.4
Experimental temperature23.0 Facility / beamlineAustralian Synchrotron / SAXS/WAXS
Wavelength0.10332 nmExposure1.0 s × 800

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Recombination directionality factor RdfS
View sequence
MKHHHHHHPMSDYDIPTTENLYFQGAMDDENDRAARAKKGSPFLNTAQAAFYIGLSQRTLEKMRLTGGGPKYRKHGRYVRYHIDELDDWSKGRPPEPGSDDDKGGSGSADEGARS
proteinMesorhizobium japonicum R7AQ7AL96—–—tetramerMolecule count 412.941 kDa
attP_8 40-mer DNA
View sequence
GAATTTCGGCGCAGTTGGTCCAACGAGGCGGGGGGCTGGT
DNA———–—dimerMolecule count 212.57 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
1670[3]0.003681128–0.3819378 1/AHas uncertainty columnMissing 0100sasbdb/entries/97/sasdw97/source/SASDW97.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)13.8—Å
i0Guinier0.0853579—1/cm
i0P(r)0.08632—1/cm
mwExperimental83.0—kDa
mwPorod88.0—kDa
porod_volumePorod134.0—ų
rgGuinier3.80.07Å
rgP(r)3.8280.07Å

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

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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 name150 mM Tris-HCl, 300 mM NaCl, 5% v/v glycerolBuffer concentration—
pH7.4Additives—
Buffer descriptionSAXS buffer, identical to SASDPK4
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2019-06-19Storage / measurement temperature23.0 / 23.0
Exposure time1.0Frames800
Wavelength0.10332Sample-to-detector distance1.6
SourceX-ray synchrotronDetectorPilatus 1M
Facility / beamlineAustralian Synchrotron / SAXS/WAXS · Melbourne, Australia
q range0.037 – 3.819Sample volume / flow rate50.0 / 0.3

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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full_entry_zip:source record and ZIP contents (6 items)
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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:196 field values
Field pathRaw value
codeSASDW97
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleStructural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS
project.publication.titleStructural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS
project.publication.author_listVerdonk C, Agostino M, Eto K, Hall D, Bond C, Ramsay J
project.publication.journalNucleic Acids Research
project.publication.doi10.1093/nar/gkaf249
project.publication.pmidnull
project.publication.published_date2025 Apr 02
project.statusreleased
project.submitted_date2025-02-11
project.released_date2025-03-29
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experiment.instrument.detector.typeDectris
experiment.instrument.detector.namePilatus 1M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameAustralian Synchrotron
experiment.instrument.cityMelbourne
experiment.instrument.countryAustralia
experiment.instrument.beamline_nameSAXS/WAXS
experiment.instrument.beam_geometryPoint
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourceTrue
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_nameRecombination directionality factor RdfS
experiment.sample.molecule[0].short_nameRdfS
experiment.sample.molecule[0].sequenceMKHHHHHHPMSDYDIPTTENLYFQGAMDDENDRAARAKKGSPFLNTAQAAFYIGLSQRTLEKMRLTGGGPKYRKHGRYVRYHIDELDDWSKGRPPEPGSDDDKGGSGSADEGARS
experiment.sample.molecule[0].organismMesorhizobium japonicum R7A
experiment.sample.molecule[0].uniprot_codeQ7AL96
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationtetramer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMDDENDRAARAKKGSPFLNTAQAAFYIGLSQRTLEKMRLTGGGPKYRKHGRYVRYHIDEL DDWSKGRPPEPGSDDDKGGSGSADEGARS
experiment.sample.molecule[0].mw12.941
experiment.sample.molecule[0].total_mw51.764
experiment.sample.molecule[0].number_molecules4
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionN-terminal Hexahistidine-tagged RdfS protein
experiment.sample.molecule[1].long_nameattP_8 40-mer DNA
experiment.sample.molecule[1].short_nameattP_8
experiment.sample.molecule[1].sequenceGAATTTCGGCGCAGTTGGTCCAACGAGGCGGGGGGCTGGT
experiment.sample.molecule[1].organismnull
experiment.sample.molecule[1].uniprot_codenull
experiment.sample.molecule[1].uniprot_range_firstnull
experiment.sample.molecule[1].uniprot_range_lastnull
experiment.sample.molecule[1].oligomerizationdimer
experiment.sample.molecule[1].molecular_typeDNA
experiment.sample.molecule[1].uniprot_sequence
experiment.sample.molecule[1].mw12.57
experiment.sample.molecule[1].total_mw25.14
experiment.sample.molecule[1].number_molecules2
experiment.sample.molecule[1].complex_stateFalse
experiment.sample.molecule[1].deuterationnull
experiment.sample.molecule[1].molecule_sourcebiological
experiment.sample.molecule[1].molecule_descriptiondsDNA 40mer oligomer synthetic DNA
experiment.sample.buffer.name150 mM Tris-HCl, 300 mM NaCl, 5% v/v glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentSAXS buffer, identical to SASDPK4
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.4
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameRecombination directionality factor (6H-RdfS) from M.japonicum bound to 40mer DNA
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].addressnull
experiment.contributor[0].affiliation[0].full_nameCurtin University
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameJoshua
experiment.contributor[0].contributor_surnameRamsay
experiment.contributor[0].orcidhttps://orcid.org/0000-0002-1301-7077
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2019-06-19
experiment.storage_temperature23.0
experiment.cell_temperature23.0
experiment.exposure_time1.0
experiment.number_of_frames800
experiment.wavelength0.10332
experiment.sample_detector_distance1.6
experiment.concentration_minnull
experiment.concentration_max6.8
experiment.sample_volume50.0
experiment.flow_rate0.3
experiment.s_min0.037
experiment.s_max3.819
experiment.total_exposure_timenull
experiment.seccolumn2
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fits[0].p_value0.0
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fits[1].p_value0.0104
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fits[1].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of His-tagged RdfS excisionase bound to dsDNA 40mer attP_8 in 150 mM Tris-HCl, 300 mM NaCl, 5% v/v glycerol, pH 7.4 were collected on the SAXS/WAXS beam line at the Australian Synchrotron (Melbourne, Australia) using a Pilatus 1M detector at a sample-detector distance of 2.6 m and at a wavelength of λ = 0.103 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 50.00 μl samples at 6H-RdfS at 390 µM, dsDNA attP_8 at 500 µM was injected at a 0.30 ml/min flow rate onto a GE Superdex 200 Increase 5/150 column at 23°C. 36 successive 1 second data frames were selected from the SEC sample peak (from a total of 800 individual frames measured from the entire SEC elution) and processed to generate the profile displayed in this entry. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[]
intensity_unit1/cm
experimental_mw83.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw88.0
porod_mw_errornull
pddf_i00.08632
pddf_i0_errornull
guinier_i00.0853579
guinier_i0_errornull
pddf_rg3.828
pddf_rg_error0.07
guinier_rg3.8
guinier_rg_error0.07
pddf_dmax13.8
pddf_dmax_errornull
porod_volume134.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first30
guinier_point_last51
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDW97_datloglog_img.png
symmetrynull
last_modified2025-04-02T23:34:23.155761+02:00
bragg_peak[]
manifest.json:34 field values
Field pathRaw value
codeSASDW97
statussuccess
started_at2026-08-11T15:24:59.569451+00:00
finished_at2026-08-11T15:25:09.584142+00:00
source_last_modified2025-04-02T23:34:23.155761+02:00
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View the complete summary.json source
{
  "code": "SASDW97",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "Structural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS",
    "publication": {
      "title": "Structural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS",
      "author_list": "Verdonk C, Agostino M, Eto K, Hall D, Bond C, Ramsay J",
      "journal": "Nucleic Acids Research",
      "doi": "10.1093/nar/gkaf249",
      "pmid": null,
      "published_date": "2025 Apr 02"
    },
    "status": "released",
    "submitted_date": "2025-02-11",
    "released_date": "2025-03-29"
  },
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        "resolution": 172.0
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      "city": "Melbourne",
      "country": "Australia",
      "beamline_name": "SAXS/WAXS",
      "beam_geometry": "Point",
      "type_of_source": "X-ray synchrotron",
      "point_source": true,
      "line_collimation": null,
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      "line_collimation_integrationwidth": null,
      "xray_energy": null,
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    },
    "sample": {
      "molecule": [
        {
          "long_name": "Recombination directionality factor RdfS",
          "short_name": "RdfS",
          "sequence": "MKHHHHHHPMSDYDIPTTENLYFQGAMDDENDRAARAKKGSPFLNTAQAAFYIGLSQRTLEKMRLTGGGPKYRKHGRYVRYHIDELDDWSKGRPPEPGSDDDKGGSGSADEGARS",
          "organism": "Mesorhizobium japonicum R7A",
          "uniprot_code": "Q7AL96",
          "uniprot_range_first": null,
          "uniprot_range_last": null,
          "oligomerization": "tetramer",
          "molecular_type": "protein",
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        "concentration_unit": null,
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    "contributor": [
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        "affiliation": [
          {
            "short_name": null,
            "address": null,
            "full_name": "Curtin University",
            "webpage": null
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        "contributor_name": "Joshua",
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  "last_modified": "2025-04-02T23:34:23.155761+02:00",
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}
View the complete manifest.json source
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