SASDEH3

TubR protein of the pXO1-like plasmid pBc10987 from B. cereus (Bc-TubR) bound to S48 DNA (Bc-TubR : S48 DNA complex)

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

The molecular weight (MW) of the Bc-TubR : S48 DNA complex was estimated from the macromolecular volume using the method of Fischer et al. (J. Appl. Crystallogr. 43, 101–109, 2010; SAXMow program). However, the MW estimate is likely not an accurate value because the sample is a complex of protein and DNA. The theoretical SAXS curve of the molecular dynamics model was calculated as the mixture of the two models (one model contains four TubR dimers plus DNA, another model contains five TubR dimers plus DNA). For the mixed model, the fractions of each are 0.4 and 0.6, respectively. A low resolution dummy atom model was built by DAMMIF. Ten independently built models were generated, spatially aligned and then bead-occupancy and volume corrected using DAMAVER to generate an averaged spatial representation of the complex (damfilt). The the fit to the SAXS data from an individual dummy atom model from the cohort of models used to obtain the average representation is shown, specifically that with the smallest chi-square value. Sample concentration: UNKNOWN

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · TubR protein of the pXO1-like plasmid pBc10987 from B. cereus (Bc-TubR) bound to S48 DNA (Bc-TubR : S48 DNA complex)

Concentration— – — Buffer / pH0.1 M NaCl, 10 mM Tris / 8.0
Experimental temperature8.0 Facility / beamlinePhoton Factory (PF), High Energy Accelerator Research Organization (KEK) / BL-10C
Wavelength0.15 nmExposure20.0 s × 1

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
S48 DNA strand 1
View sequence
ATCATACTTCGGAAATATATACCGAAGTATTTACGGCTTTTATAACGGTATTAAATTCCGTATAATGAT
DNA———–—monomerMolecule count 121.324 kDa
S48 DNA strand 2
View sequence
ATCATACTTCGGAAATATATACCGAAGTATTTACGGCTTTTATAACGGTATTAAATTCCGTATAATGAT
DNA———–—monomerMolecule count 121.324 kDa
TubR of the pXO1-like plasmid pBc10987 from B. cereus (Bc-TubR)
View sequence
GSHMSNISMSSSEIIDVLCENLNDGIWALRVLYAEGAMNKEKLWDYINQYHKDYQIENEKDYEGKKILPSRYALDIMTARLEGAGLISFKAIGRVRIYDVTDLGNVLIKELEKRVEKNN
protein—B7JTH01–116decamerMolecule count 1013.685 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
1757[3]0.00787803–0.2781353 1/AHas uncertainty columnMissing 013sasbdb/entries/h3/sasdeh3/source/SASDEH3.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)23.0—Å
i0Guinier0.079520.00031/cm
i0P(r)0.08148—1/cm
mwExperimental249.0—kDa
porod_volumePorod305.0—ų
rgGuinier6.110.04Å
rgP(r)6.57—Å

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

▼

3. Source Fits and Models Source Fits & Models

Fit 1 · CRYSOL

χ²: 0.8963CorMap p: 0.0Unit: 1/A
ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—atomicMolecular Dynamics Frame —174.8—Model Image
2—atomicMolecular Dynamics Frame —148.1—Model Image

Fit 2 · DAMMIF

χ²: 0.907CorMap p: 0.0Unit: 1/A
ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—dummyDAMFILT DAMFILT 5.———Model Image
▶

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 name0.1 M NaCl, 10 mM TrisBuffer concentration—
pH8.0Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2017-11-28Storage / measurement temperature8.0 / 8.0
Exposure time20.0Frames1
Wavelength0.15Sample-to-detector distance2.012
SourceX-ray synchrotronDetectorPilatus3 2M
Facility / beamlinePhoton Factory (PF), High Energy Accelerator Research Organization (KEK) / BL-10C · Tsukuba, Japan
q range0.079 – 2.781Sample volume / flow rate— / —

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

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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:226 field values
Field pathRaw value
codeSASDEH3
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleCooperative DNA Binding of the Plasmid Partitioning Protein TubR from the Bacillus cereus pXO1 Plasmid.
project.publication.titleCooperative DNA Binding of the Plasmid Partitioning Protein TubR from the Bacillus cereus pXO1 Plasmid.
project.publication.author_listHayashi I, Oda T, Sato M, Fuchigami S
project.publication.journalJ Mol Biol
project.publication.doi10.1016/j.jmb.2018.11.001
project.publication.pmid30414406
project.publication.published_date2018 Nov 7
project.statusreleased
project.submitted_date2018-08-23
project.released_date2018-11-13
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDEH3.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDEH3.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEH3_dat_img.png
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pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDEH3_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEH3_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDEH3.sascif
experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus3 2M
experiment.instrument.detector.resolution0.172
experiment.instrument.namePhoton Factory (PF), High Energy Accelerator Research Organization (KEK)
experiment.instrument.cityTsukuba
experiment.instrument.countryJapan
experiment.instrument.beamline_nameBL-10C
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_nameS48 DNA strand 1
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceATCATACTTCGGAAATATATACCGAAGTATTTACGGCTTTTATAACGGTATTAAATTCCGTATAATGAT
experiment.sample.molecule[0].organismnull
experiment.sample.molecule[0].uniprot_codenull
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeDNA
experiment.sample.molecule[0].uniprot_sequencenull
experiment.sample.molecule[0].mw21.324
experiment.sample.molecule[0].total_mw21.324
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.molecule[1].long_nameS48 DNA strand 2
experiment.sample.molecule[1].short_namenull
experiment.sample.molecule[1].sequenceATCATACTTCGGAAATATATACCGAAGTATTTACGGCTTTTATAACGGTATTAAATTCCGTATAATGAT
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].oligomerizationmonomer
experiment.sample.molecule[1].molecular_typeDNA
experiment.sample.molecule[1].uniprot_sequencenull
experiment.sample.molecule[1].mw21.324
experiment.sample.molecule[1].total_mw21.324
experiment.sample.molecule[1].number_molecules1
experiment.sample.molecule[1].complex_stateFalse
experiment.sample.molecule[1].deuterationnull
experiment.sample.molecule[1].molecule_sourcebiological
experiment.sample.molecule[1].molecule_descriptionnull
experiment.sample.molecule[2].long_nameTubR of the pXO1-like plasmid pBc10987 from B. cereus (Bc-TubR)
experiment.sample.molecule[2].short_nameBc-TubR
experiment.sample.molecule[2].sequenceGSHMSNISMSSSEIIDVLCENLNDGIWALRVLYAEGAMNKEKLWDYINQYHKDYQIENEKDYEGKKILPSRYALDIMTARLEGAGLISFKAIGRVRIYDVTDLGNVLIKELEKRVEKNN
experiment.sample.molecule[2].organismnull
experiment.sample.molecule[2].uniprot_codeB7JTH0
experiment.sample.molecule[2].uniprot_range_first1
experiment.sample.molecule[2].uniprot_range_last116
experiment.sample.molecule[2].oligomerizationdecamer
experiment.sample.molecule[2].molecular_typeprotein
experiment.sample.molecule[2].uniprot_sequenceMSNISMSSSEIIDVLCENLNDGIWALRVLYAEGAMNKEKLWDYINQYHKDYQIENEKDYE GKKILPSRYALDIMTARLEGAGLISFKAIGRVRIYDVTDLGNVLIKELEKRVEKNN
experiment.sample.molecule[2].mw13.685
experiment.sample.molecule[2].total_mw136.85
experiment.sample.molecule[2].number_molecules10
experiment.sample.molecule[2].complex_stateFalse
experiment.sample.molecule[2].deuterationnull
experiment.sample.molecule[2].molecule_sourcebiological
experiment.sample.molecule[2].molecule_descriptionnull
experiment.sample.buffer.name0.1 M NaCl, 10 mM Tris
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.nameTubR protein of the pXO1-like plasmid pBc10987 from B. cereus (Bc-TubR) bound to S48 DNA (Bc-TubR : S48 DNA complex)
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].addressJapan
experiment.contributor[0].affiliation[0].full_nameYokohama City University
experiment.contributor[0].affiliation[0].webpagehttps://www.yokohama-cu.ac.jp
experiment.contributor[0].contributor_nameTakashi
experiment.contributor[0].contributor_surnameOda
experiment.contributor[0].orcid
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2017-11-28
experiment.storage_temperature8.0
experiment.cell_temperature8.0
experiment.exposure_time20.0
experiment.number_of_frames1
experiment.wavelength0.15
experiment.sample_detector_distance2.012
experiment.concentration_minnull
experiment.concentration_maxnull
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.079
experiment.s_max2.781
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].models[0].pdb_link[]
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fits[0].models[0].type_of_modelatomic
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fits[0].softwareCRYSOL
fits[0].chi_square_value0.8963
fits[0].p_value0.0
fits[0].fit_residual_plotFrction_0_fitresiduals_img.png
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fits[1].models[0].pdb_link[]
fits[1].models[0].model_titlenull
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fits[1].models[0].software_versionDAMFILT 5.
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fits[1].softwareDAMMIF
fits[1].chi_square_value0.907
fits[1].p_value0.0
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fits[1].software_versionnull
fits[1].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionThe molecular weight (MW) of the Bc-TubR : S48 DNA complex was estimated from the macromolecular volume using the method of Fischer et al. (J. Appl. Crystallogr. 43, 101–109, 2010; SAXMow program). However, the MW estimate is likely not an accurate value because the sample is a complex of protein and DNA. The theoretical SAXS curve of the molecular dynamics model was calculated as the mixture of the two models (one model contains four TubR dimers plus DNA, another model contains five TubR dimers plus DNA). For the mixed model, the fractions of each are 0.4 and 0.6, respectively. A low resolution dummy atom model was built by DAMMIF. Ten independently built models were generated, spatially aligned and then bead-occupancy and volume corrected using DAMAVER to generate an averaged spatial representation of the complex (damfilt). The the fit to the SAXS data from an individual dummy atom model from the cohort of models used to obtain the average representation is shown, specifically that with the smallest chi-square value. Sample concentration: UNKNOWN
experiment_descriptionSynchrotron SAXS data from a solution of the Bc-TubR:S48 DNA complex in 0.1 M NaCl, 10 mM Tris, pH 8 were collected on the BL-10C beam line at the Photon Factory (PF), High Energy Accelerator Research Organization (KEK) storage ring (Tsukuba, Japan) using a Pilatus3 2M detector at a sample-detector distance of 2.0 m and at a wavelength of λ = 0.15 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Data were collected for a 20 s X-ray exposure time at a sample temperature of 8°C. 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_mw249.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i00.08148
pddf_i0_errornull
guinier_i00.07952
guinier_i0_error0.0003
pddf_rg6.57
pddf_rg_errornull
guinier_rg6.11
guinier_rg_error0.04
pddf_dmax23.0
pddf_dmax_errornull
porod_volume305.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last39
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDEH3_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDEH3
statussuccess
started_at2026-08-11T14:00:37.680428+00:00
finished_at2026-08-11T14:00:50.695617+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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View the complete summary.json source
{
  "code": "SASDEH3",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
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    "title": "Cooperative DNA Binding of the Plasmid Partitioning Protein TubR from the Bacillus cereus pXO1 Plasmid.",
    "publication": {
      "title": "Cooperative DNA Binding of the Plasmid Partitioning Protein TubR from the Bacillus cereus pXO1 Plasmid.",
      "author_list": "Hayashi I, Oda T, Sato M, Fuchigami S",
      "journal": "J Mol Biol",
      "doi": "10.1016/j.jmb.2018.11.001",
      "pmid": "30414406",
      "published_date": "2018 Nov 7"
    },
    "status": "released",
    "submitted_date": "2018-08-23",
    "released_date": "2018-11-13"
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      "name": "Photon Factory (PF), High Energy Accelerator Research Organization (KEK)",
      "city": "Tsukuba",
      "country": "Japan",
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      "beam_geometry": null,
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          "long_name": "S48 DNA strand 1",
          "short_name": null,
          "sequence": "ATCATACTTCGGAAATATATACCGAAGTATTTACGGCTTTTATAACGGTATTAAATTCCGTATAATGAT",
          "organism": null,
          "uniprot_code": null,
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          "oligomerization": "monomer",
          "molecular_type": "DNA",
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          "number_molecules": 1,
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          "molecule_description": null
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          "long_name": "S48 DNA strand 2",
          "short_name": null,
          "sequence": "ATCATACTTCGGAAATATATACCGAAGTATTTACGGCTTTTATAACGGTATTAAATTCCGTATAATGAT",
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          "oligomerization": "monomer",
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          "number_molecules": 1,
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          "molecule_source": "biological",
          "molecule_description": null
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        {
          "long_name": "TubR of the pXO1-like plasmid pBc10987 from B. cereus (Bc-TubR)",
          "short_name": "Bc-TubR",
          "sequence": "GSHMSNISMSSSEIIDVLCENLNDGIWALRVLYAEGAMNKEKLWDYINQYHKDYQIENEKDYEGKKILPSRYALDIMTARLEGAGLISFKAIGRVRIYDVTDLGNVLIKELEKRVEKNN",
          "organism": null,
          "uniprot_code": "B7JTH0",
          "uniprot_range_first": 1,
          "uniprot_range_last": 116,
          "oligomerization": "decamer",
          "molecular_type": "protein",
          "uniprot_sequence": "MSNISMSSSEIIDVLCENLNDGIWALRVLYAEGAMNKEKLWDYINQYHKDYQIENEKDYE\nGKKILPSRYALDIMTARLEGAGLISFKAIGRVRIYDVTDLGNVLIKELEKRVEKNN",
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          "number_molecules": 10,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
      ],
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        "name": "0.1 M NaCl, 10 mM Tris",
        "concentration_unit": null,
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        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 8.0,
        "deuteration": null
      },
      "purity_method": null,
      "name": "TubR protein of the pXO1-like plasmid pBc10987 from B. cereus (Bc-TubR) bound to S48 DNA (Bc-TubR : S48 DNA complex)",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
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    "contributor": [
      {
        "affiliation": [
          {
            "short_name": null,
            "address": "Japan",
            "full_name": "Yokohama City University",
            "webpage": "https://www.yokohama-cu.ac.jp"
          }
        ],
        "contributor_name": "Takashi",
        "contributor_surname": "Oda",
        "orcid": ""
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    "concentration_unit": null,
    "date": "2017-11-28",
    "storage_temperature": 8.0,
    "cell_temperature": 8.0,
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    "wavelength": 0.15,
    "sample_detector_distance": 2.012,
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  "last_modified": "2019-12-06T13:07:15.624532+01:00",
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}
View the complete manifest.json source
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