SASDFE8

Histidine-binding periplasmic protein (HisBP) in the presence of histidine - His-bound 5-fold excess

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

His-bound HisBP at a ligand:protein ratio of 5:1. Ligand condition is prepared by dissolving histidine in powder form (Sigma-Aldrich) directly into the SAXS buffer, followed by dilution to the target concentration with additional SAXS buffer.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Histidine-binding periplasmic protein (HisBP) in the presence of histidine - His-bound 5-fold excess

Concentration— – 4.2 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 02sasbdb/entries/e8/sasdfe8/source/SASDFE8.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)5.71—nm
i0Guinier128.710.1arbitrary
i0P(r)128.8—arbitrary
mwExperimental30.0—kDa
mwPorod21.0—kDa
porod_volumePorod33.0—nm³
rgGuinier1.830.0nm
rgP(r)1.833—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
codeSASDFE8
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.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
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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) in the presence of histidine - His-bound 5-fold excess
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
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experiment.s_min0.031
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experiment.seccolumnnull
fits[]
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionHis-bound HisBP at a ligand:protein ratio of 5:1. Ligand condition is prepared by dissolving histidine in powder form (Sigma-Aldrich) directly into the SAXS buffer, followed by dilution to the target concentration with additional SAXS buffer.
experiment_descriptionSynchrotron SAXS data from solutions of HisBP with a 5-fold excess of histidine 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 4.20 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[]
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pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDFE8_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDFE8
statussuccess
started_at2026-08-11T15:51:34.601454+00:00
finished_at2026-08-11T15:51:42.472984+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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View the complete summary.json source
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  "code": "SASDFE8",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
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    "title": "Structure-based screening of binding affinities via small-angle X-ray scattering",
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      "journal": null,
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      "pmid": null,
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View the complete manifest.json source
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