SASDFD8

Histidine-binding periplasmic protein (HisBP), apo-form

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

Free HisBP after TEV cleavage to remove hexahistidine tags, followed by reverse His-Trap and SEC column purification. Note N-terminal glycine before the Uniprot sequence due to TEV tag.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Histidine-binding periplasmic protein (HisBP), apo-form

Concentration— – 4.25 Buffer / pH100 mM NaCl, 20 mM NaPO4, 0.5 mM TCEP / 7.4
Experimental temperature20.0 Facility / beamlineESRF / BM29
Wavelength0.09919 nmExposure2.0 s × 12

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Histidine-binding periplasmic protein
View sequence
GAIPQNIRIGTDPTYAPFESKNSQGELVGFDIDLAKELCKRINTQCTFVENPLDALIPSLKAKKIDAIMSSLSITEKRQQEIAFTDKLYAADSRLVVAKNSDIQPTVESLKGKRVGVLQGTTQETFGNEHWAPKGIEIVSYQGQDNIYSDLTAGRIDAAFQDEVAASEGFLKQPVGKDYKFGGPSVKDEKLFGVGTGMGLRKEDNELREALNKAFAEMRADGTYEKLAKKYFDFDVYGG
proteinEscherichia coliP0AEU023–260monomerMolecule count 126.289 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11043[3]0.03059113–4.946227 1/nmHas uncertainty columnMissing 04sasbdb/entries/d8/sasdfd8/source/SASDFD8.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)6.03—nm
i0Guinier124.420.1arbitrary
i0P(r)124.7—arbitrary
mwExperimental29.6—kDa
mwGuinier I(0)29.6—kDa
mwPorod20.0—kDa
porod_volumePorod32.0—nm³
rgGuinier1.960.07nm
rgP(r)1.975—nm

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

This entry has no source fit record.

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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 name100 mM NaCl, 20 mM NaPO4, 0.5 mM TCEPBuffer concentration—
pH7.4Additives—
Buffer descriptionSEC buffer for PBP experiments
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2018-09-10Storage / measurement temperature— / 20.0
Exposure time2.0Frames12
Wavelength0.09919Sample-to-detector distance2.849
SourceX-ray synchrotronDetectorPilatus 1M
Facility / beamlineESRF / BM29 · Grenoble, France
q range0.031 – 4.946Sample 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

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:134 field values
Field pathRaw value
codeSASDFD8
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleStructure-based screening of binding affinities via small-angle X-ray scattering
project.publication.titleStructure-based screening of binding affinities via small-angle X-ray scattering
project.publication.author_listChen P, Masiewicz P, Perez K, Hennig J
project.publication.journalnull
project.publication.doi10.1101/715193
project.publication.pmidnull
project.publication.published_date2019 Jul 31
project.statusreleased
project.submitted_date2019-07-01
project.released_date2019-08-02
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experiment.instrument.detector.typeDectris
experiment.instrument.detector.namePilatus 1M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameESRF
experiment.instrument.cityGrenoble
experiment.instrument.countryFrance
experiment.instrument.beamline_nameBM29
experiment.instrument.beam_geometry
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
experiment.instrument.line_collimationnull
experiment.instrument.sample_path_lengthnull
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experiment.instrument.xray_energynull
experiment.instrument.beam_profile_ahnull
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experiment.sample.molecule[0].long_nameHistidine-binding periplasmic protein
experiment.sample.molecule[0].short_nameHisBP
experiment.sample.molecule[0].sequenceGAIPQNIRIGTDPTYAPFESKNSQGELVGFDIDLAKELCKRINTQCTFVENPLDALIPSLK AKKIDAIMSSLSITEKRQQEIAFTDKLYAADSRLVVAKNSDIQPTVESLKGKRVGVLQGT TQETFGNEHWAPKGIEIVSYQGQDNIYSDLTAGRIDAAFQDEVAASEGFLKQPVGKDYKF GGPSVKDEKLFGVGTGMGLRKEDNELREALNKAFAEMRADGTYEKLAKKYFDFDVYGG
experiment.sample.molecule[0].organismEscherichia coli
experiment.sample.molecule[0].uniprot_codeP0AEU0
experiment.sample.molecule[0].uniprot_range_first23
experiment.sample.molecule[0].uniprot_range_last260
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMKKLVLSLSLVLAFSSATAAFAAIPQNIRIGTDPTYAPFESKNSQGELVGFDIDLAKELC KRINTQCTFVENPLDALIPSLKAKKIDAIMSSLSITEKRQQEIAFTDKLYAADSRLVVAK NSDIQPTVESLKGKRVGVLQGTTQETFGNEHWAPKGIEIVSYQGQDNIYSDLTAGRIDAA FQDEVAASEGFLKQPVGKDYKFGGPSVKDEKLFGVGTGMGLRKEDNELREALNKAFAEMR ADGTYEKLAKKYFDFDVYGG
experiment.sample.molecule[0].mw26.289
experiment.sample.molecule[0].total_mw26.289
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.name100 mM NaCl, 20 mM NaPO4, 0.5 mM TCEP
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentSEC buffer for PBP experiments
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.nameHistidine-binding periplasmic protein (HisBP), apo-form
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_nameEMBL
experiment.contributor[0].affiliation[0].addressHeidelberg, Germany
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Heidelberg
experiment.contributor[0].affiliation[0].webpagehttps://www.embl.de/
experiment.contributor[0].contributor_namePo-chia
experiment.contributor[0].contributor_surnameChen
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2018-09-10
experiment.storage_temperaturenull
experiment.cell_temperature20.0
experiment.exposure_time2.0
experiment.number_of_frames12
experiment.wavelength0.09919
experiment.sample_detector_distance2.849
experiment.concentration_minnull
experiment.concentration_max4.25
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.031
experiment.s_max4.946
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[]
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionFree HisBP after TEV cleavage to remove hexahistidine tags, followed by reverse His-Trap and SEC column purification. Note N-terminal glycine before the Uniprot sequence due to TEV tag.
experiment_descriptionSynchrotron SAXS data from solutions of HisBP, apo-form, in 100 mM NaCl, 20 mM NaPO4, 0.5 mM TCEP, pH 7.4 were collected on the BM29 beam line at the ESRF (Grenoble, France) using a Pilatus 1M detector at a sample-detector distance of 2.8 m and at a wavelength of λ = 0.09919 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 4.25 mg/ml was measured at 20°C. 12 successive 2 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[]
intensity_unitarbitrary
experimental_mw29.6
experimental_mw_errornull
guinier_i0_mw29.6
guinier_i0_mw_errornull
porod_mw20.0
porod_mw_errornull
pddf_i0124.7
pddf_i0_errornull
guinier_i0124.42
guinier_i0_error0.1
pddf_rg1.975
pddf_rg_errornull
guinier_rg1.96
guinier_rg_error0.07
pddf_dmax6.03
pddf_dmax_errornull
porod_volume32.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first21
guinier_point_last134
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDFD8_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDFD8
statussuccess
started_at2026-08-11T15:50:55.409164+00:00
finished_at2026-08-11T15:51:03.357227+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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View the complete summary.json source
{
  "code": "SASDFD8",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
  "project": {
    "title": "Structure-based screening of binding affinities via small-angle X-ray scattering",
    "publication": {
      "title": "Structure-based screening of binding affinities via small-angle X-ray scattering",
      "author_list": "Chen P, Masiewicz P, Perez K, Hennig J",
      "journal": null,
      "doi": "10.1101/715193",
      "pmid": null,
      "published_date": "2019 Jul 31"
    },
    "status": "released",
    "submitted_date": "2019-07-01",
    "released_date": "2019-08-02"
  },
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          "long_name": "Histidine-binding periplasmic protein",
          "short_name": "HisBP",
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          "uniprot_range_last": 260,
          "oligomerization": "monomer",
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  "tags": [],
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  "porod_mw": 20.0,
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  "pddf_i0": 124.7,
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View the complete manifest.json source
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