SASDA96

Lysozyme

Data type: SASBDB experimental data Status: Published Curve type: Single concentration Last updated: 2023-06-21T07:56:39.492710+02:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Lysozyme

Concentration— – 2.61 mg/mlBuffer / pH20 mM Sodium Acetate/HEPES / 6.8
Experimental temperature10.0 Facility / beamlinePETRA III / EMBL P12
Wavelength0.12 nmExposure0.05 s × 20

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Lysozyme C
View sequence
KVFGRCELAAAMKRHGLDNYRGYSLGNWVCAAKFESNFNTQATNRNTDGSTDYGILQINSRWWCNDGRTPGSRNLCNIPCSALLSSDITASVNCAKKIVSDGNGMNAWVAWRNRCKGTDVQAWIRGCRL
proteinGallus gallusP0069819–147monomerMolecule count 114.31 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11366[3]0.166206–3.78909 1/nmHas uncertainty columnMissing 025sasbdb/entries/96/sasda96/source/SASDA96.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)4.79—nm
i0Guinier779.5——
i0P(r)780.5——
mwExperimental14.8—kDa
mwGuinier I(0)14.8—kDa
mwPorod13.93—kDa
porod_volumePorod23.69—nm³
rgGuinier1.5—nm
rgP(r)1.51—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

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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 name20 mM Sodium Acetate/HEPESBuffer concentration20.0 mM
pH6.8Additives—
Buffer descriptionMixed Buffer
Purity measurement method—Extinction coefficient2.653
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2013-02-17Storage / measurement temperature10.0 / 10.0
Exposure time0.05Frames20
Wavelength0.12Sample-to-detector distance3.1
SourceX-ray synchrotronDetectorPilatus 2M
Facility / beamlinePETRA III / EMBL P12 · DESY; Hamburg, Germany
q range0.166 – 3.789Sample 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:222 field values
Field pathRaw value
codeSASDA96
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleCorrelation Map, a goodness-of-fit test for one-dimensional X-ray scattering spectra.
project.publication.titleCorrelation Map, a goodness-of-fit test for one-dimensional X-ray scattering spectra.
project.publication.author_listFranke D, Jeffries CM, Svergun DI
project.publication.journalNat Methods
project.publication.doi10.1038/nmeth.3358
project.publication.pmid25849637
project.publication.published_date2015 May
project.statusreleased
project.submitted_datenull
project.released_date2015-05-01
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experiment.instrument.detector.namePilatus 2M
experiment.instrument.detector.resolutionnull
experiment.instrument.namePETRA III
experiment.instrument.cityDESY; Hamburg
experiment.instrument.countryGermany
experiment.instrument.beamline_nameEMBL P12
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_nameLysozyme C
experiment.sample.molecule[0].short_nameLysozyme, lys
experiment.sample.molecule[0].sequenceKVFGRCELAAAMKRHGLDNYRGYSLGNWVCAAKFESNFNTQA TNRNTDGSTDYGILQINSRWWCNDGRTPGSRNLCNIPCSALLSSDITASVNCAKKIVSDG NGMNAWVAWRNRCKGTDVQAWIRGCRL
experiment.sample.molecule[0].organismGallus gallus
experiment.sample.molecule[0].uniprot_codeP00698
experiment.sample.molecule[0].uniprot_range_first19
experiment.sample.molecule[0].uniprot_range_last147
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMRSLLILVLCFLPLAALGKVFGRCELAAAMKRHGLDNYRGYSLGNWVCAAKFESNFNTQA TNRNTDGSTDYGILQINSRWWCNDGRTPGSRNLCNIPCSALLSSDITASVNCAKKIVSDG NGMNAWVAWRNRCKGTDVQAWIRGCRL
experiment.sample.molecule[0].mw14.31
experiment.sample.molecule[0].total_mw14.31
experiment.sample.molecule[0].number_molecules1
experiment.sample.molecule[0].complex_statenull
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_description
experiment.sample.buffer.name20 mM Sodium Acetate/HEPES
experiment.sample.buffer.concentration_unitmM
experiment.sample.buffer.commentMixed Buffer
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentration20.0
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph6.8
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameLysozyme
experiment.sample.ext_coefficient2.653
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-Hamburg
experiment.contributor[0].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[0].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[0].contributor_nameDaniel
experiment.contributor[0].contributor_surnameFranke
experiment.contributor[0].orcidnull
experiment.contributor[1].affiliation[0].short_nameEMBL-Hamburg
experiment.contributor[1].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[1].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[1].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[1].contributor_nameCy M
experiment.contributor[1].contributor_surnameJeffries
experiment.contributor[1].orcidnull
experiment.contributor[2].affiliation[0].short_nameEMBL-Hamburg
experiment.contributor[2].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[2].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[2].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[2].contributor_nameDmitri
experiment.contributor[2].contributor_surnameSvergun
experiment.contributor[2].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitmg/ml
experiment.date2013-02-17
experiment.storage_temperature10.0
experiment.cell_temperature10.0
experiment.exposure_time0.05
experiment.number_of_frames20
experiment.wavelength0.12
experiment.sample_detector_distance3.1
experiment.concentration_minnull
experiment.concentration_max2.61
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.166
experiment.s_max3.789
experiment.total_exposure_timenull
experiment.seccolumnnull
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pddf_softwareATSAS GNOM
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i0_calibration_standardBovine Serum Albumin
descriptionnull
experiment_descriptionX-ray synchrotron radiation scattering data from a solution of Lysozyme C in 20 mM Sodium Acetate/HEPES, pH 6.8 were collected on the P12 beam line at Petra-III (Hamburg, Germany) using a Pilatus 2M detector (I(s) vs s, where s = 4π sin θ/λ; 2θ is the scattering angle and λ = 0.12 nm). One solute concentration at 2.61 mg/ml was measured using a total exposure time of 1 second (20 x 0.050 second frames). The data were normalized to the intensity of the transmitted beam and radially averaged. Scattering contributions from the matched solvent blank were subtracted and the resulting 1D scattering data were scaled to protein concentration. The data presented in this entry were obtained from a single concentration scattering curve.
tags[0]benchmark
intensity_unitnull
experimental_mw14.8
experimental_mw_errornull
guinier_i0_mw14.8
guinier_i0_mw_errornull
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pddf_dmax_errornull
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symmetrynull
last_modified2023-06-21T07:56:39.492710+02:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDA96
statussuccess
started_at2026-08-11T15:04:16.005924+00:00
finished_at2026-08-11T15:04:24.766441+00:00
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View the complete summary.json source
{
  "code": "SASDA96",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
  "project": {
    "title": "Correlation Map, a goodness-of-fit test for one-dimensional X-ray scattering spectra.",
    "publication": {
      "title": "Correlation Map, a goodness-of-fit test for one-dimensional X-ray scattering spectra.",
      "author_list": "Franke D, Jeffries CM, Svergun DI",
      "journal": "Nat Methods",
      "doi": "10.1038/nmeth.3358",
      "pmid": "25849637",
      "published_date": "2015 May"
    },
    "status": "released",
    "submitted_date": null,
    "released_date": "2015-05-01"
  },
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View the complete manifest.json source
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