SASDCK2

Glucose Isomerase - Streptomyces rubiginosus

Data type: SASBDB experimental data Status: Published Curve type: Other Last updated: 2024-03-08T11:32:18.321280+01:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Glucose Isomerase - Streptomyces rubiginosus

Concentration0.06 – 0.34 Buffer / pH25 mM MOPS, 250 mM NaCl, 50 mM KCl, 2 mM TCEP, 0.1% NaN3 / 7.5
Experimental temperature22.0 Facility / beamlineAustralian Synchrotron / SAXS/WAXS
Wavelength0.10332 nmExposure1.0 s × 24

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Xylose isomerase
View sequence
MNYQPTPEDRFTFGLWTVGWQGRDPFGDATRRALDPVESVRRLAELGAHGVTFHDDDLIPFGSSDSEREEHVKRFRQALDDTGMKVPMATTNLFTHPVFKDGGFTANDRDVRRYALRKTIRNIDLAVELGAETYVAWGGREGAESGGAKDVRDALDRMKEAFDLLGEYVTSQGYDIRFAIEPKPNEPRGDILLPTVGHALAFIERLERPELYGVNPEVGHEQMAGLNFPHGIAQALWAGKLFHIDLNGQNGIKYDQDLRFGAGDLRAAFWLVDLLESAGYSGPRHFDFKPPRTEDFDGVWASAAGCMRNYLILKERAAAFRADPEVQEALRASRLDELARPTAADGLQALLDDRSAFEEFDVDAAAARGMAFERLDQLAMDHLLGARG
proteinStreptomyces rubiginosusP243001–388tetramerMolecule count 443.227 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
1392[3]0.0066275299–0.3104110062 1/AHas uncertainty columnMissing 035sasbdb/entries/k2/sasdck2/source/SASDCK2.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)9.22—Å
i0Guinier0.0374.4e-051/cm
i0P(r)0.037393.9e-051/cm
mwExperimental172.234—kDa
mwGuinier I(0)183.254—kDa
mwPorod152.667—kDa
porod_volumePorod229.0—ų
rgGuinier3.2870.013Å
rgP(r)3.2650.004Å

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 name25 mM MOPS, 250 mM NaCl, 50 mM KCl, 2 mM TCEP, 0.1% NaN3Buffer concentration—
pH7.5Additives—
Buffer description2 mM TCEP and 0.1% (.01538 M) NaN3 used for radiation protection
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2017-03-09Storage / measurement temperature— / 22.0
Exposure time1.0Frames24
Wavelength0.10332Sample-to-detector distance2.683
SourceX-ray synchrotronDetectorPilatus 1M
Facility / beamlineAustralian Synchrotron / SAXS/WAXS · Melbourne, Australia
q range0.066 – 3.104Sample 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:182 field values
Field pathRaw value
codeSASDCK2
statusPublished
type_of_curveOther
angular_unit1/A
project.title2017 publication guidelines for structural modelling of small-angle scattering data from biomolecules in solution: an update.
project.publication.title2017 publication guidelines for structural modelling of small-angle scattering data from biomolecules in solution: an update.
project.publication.author_listTrewhella J, Duff AP, Durand D, Gabel F, Guss JM, Hendrickson WA, Hura GL, Jacques DA, Kirby NM, Kwan AH, Pérez J, Pollack L, Ryan TM, Sali A, Schneidman-Duhovny D, Schwede T, Svergun DI, Sugiyama M, Tainer JA, Vachette P, Westbrook J, Whitten AE
project.publication.journalActa Crystallogr D Struct Biol
project.publication.doi10.1107/S2059798317011597
project.publication.pmid28876235
project.publication.published_date2017 Sep 1
project.statusreleased
project.submitted_date2017-05-06
project.released_date2017-08-22
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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_nameXylose isomerase
experiment.sample.molecule[0].short_nameGlucose Isomerase
experiment.sample.molecule[0].sequenceMNYQPTPEDRFTFGLWTVGWQGRDPFGDATRRALDPVESVRRLAELGAHGVTFHDDDLIP FGSSDSEREEHVKRFRQALDDTGMKVPMATTNLFTHPVFKDGGFTANDRDVRRYALRKTI RNIDLAVELGAETYVAWGGREGAESGGAKDVRDALDRMKEAFDLLGEYVTSQGYDIRFAI EPKPNEPRGDILLPTVGHALAFIERLERPELYGVNPEVGHEQMAGLNFPHGIAQALWAGK LFHIDLNGQNGIKYDQDLRFGAGDLRAAFWLVDLLESAGYSGPRHFDFKPPRTEDFDGVW ASAAGCMRNYLILKERAAAFRADPEVQEALRASRLDELARPTAADGLQALLDDRSAFEEF DVDAAAARGMAFERLDQLAMDHLLGARG
experiment.sample.molecule[0].organismStreptomyces rubiginosus
experiment.sample.molecule[0].uniprot_codeP24300
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last388
experiment.sample.molecule[0].oligomerizationtetramer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMNYQPTPEDRFTFGLWTVGWQGRDPFGDATRRALDPVESVRRLAELGAHGVTFHDDDLIP FGSSDSEREEHVKRFRQALDDTGMKVPMATTNLFTHPVFKDGGFTANDRDVRRYALRKTI RNIDLAVELGAETYVAWGGREGAESGGAKDVRDALDRMKEAFDLLGEYVTSQGYDIRFAI EPKPNEPRGDILLPTVGHALAFIERLERPELYGVNPEVGHEQMAGLNFPHGIAQALWAGK LFHIDLNGQNGIKYDQDLRFGAGDLRAAFWLVDLLESAGYSGPRHFDFKPPRTEDFDGVW ASAAGCMRNYLILKERAAAFRADPEVQEALRASRLDELARPTAADGLQALLDDRSAFEEF DVDAAAARGMAFERLDQLAMDHLLGARG
experiment.sample.molecule[0].mw43.227
experiment.sample.molecule[0].total_mw172.908
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_description
experiment.sample.buffer.name25 mM MOPS, 250 mM NaCl, 50 mM KCl, 2 mM TCEP, 0.1% NaN3
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.comment2 mM TCEP and 0.1% (.01538 M) NaN3 used for radiation protection
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameGlucose Isomerase - Streptomyces rubiginosus
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].addressSydney, New South Wales 2006, Australia
experiment.contributor[0].affiliation[0].full_nameSchool of Molecular Bioscience, University of Sydney.
experiment.contributor[0].affiliation[0].webpage
experiment.contributor[0].contributor_nameJill
experiment.contributor[0].contributor_surnameTrewhella
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2017-03-09
experiment.storage_temperaturenull
experiment.cell_temperature22.0
experiment.exposure_time1.0
experiment.number_of_frames24
experiment.wavelength0.10332
experiment.sample_detector_distance2.683
experiment.concentration_min0.06
experiment.concentration_max0.34
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.066
experiment.s_max3.104
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].models[0].commentjob submitted ATSAS on-line April 9, 2017
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fits[1].models[0].bead_radius1.9
fits[1].models[0].lognull
fits[1].models[0].symmetry
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fits[1].models[0].user138
fits[1].fit_unit1/A
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fits[1].softwareFoXS
fits[1].chi_square_value1.02
fits[1].p_value0.045511
fits[1].fit_residual_plotSASDCK2_fit2_fitfoxsresiduals_img.png
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estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versionGNOM
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of glucoes isomerase in 25 mM MOPS, 250 mM NaCl, 50 mM KCl, 2 mM TCEP, 0.1% NaN3, pH 7.5 were collected on the SAXS/WAXS beam line at Australian Synchrotron (Melbourne, Australia) using a Pilatus 1M detector at a sample-detector distance of 2.7 m and at a wavelength of λ = 0.10332 nm (I(s) vs s, where s = 4πsinθ/λ and 2θ is the scattering angle). Scattering data are on an absolute scale (cm-1) set by reference to the scattering from pure H2O. I(0) values must be corrected for the shear flow sample cell by a 2.05 multiplicative factor. Data were acquired in SEC-SAXS mode, summed from 21 measurement frames where Rg was flat and at a maximum. The average concentration over the frames was 0.18 mg/mL, spanning values from 0.06 - 0.34 mg/mL. Sample concentrations were measured by A280 (extinction coefficient for 1 mg/mL, 10 mm pathlength; E0.1% = 1.079), corrected for the 3.1 mm path-length of the UV measurement cell. MULCh was used to calculate the partial specific volume (0.732 mL/g) and X-ray contrast (Δρ = 2.833e10 cm-2). The protein is a tetramer in the solution conditions measured.
tags[0]benchmark
intensity_unit1/cm
experimental_mw172.234
experimental_mw_errornull
guinier_i0_mw183.254
guinier_i0_mw_errornull
porod_mw152.667
porod_mw_errornull
pddf_i00.03739
pddf_i0_error3.9e-05
guinier_i00.037
guinier_i0_error4.4e-05
pddf_rg3.265
pddf_rg_error0.004
guinier_rg3.287
guinier_rg_error0.013
pddf_dmax9.22
pddf_dmax_errornull
porod_volume229.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last43
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDCK2_datloglog_img.png
symmetrynull
last_modified2024-03-08T11:32:18.321280+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDCK2
statussuccess
started_at2026-08-11T13:40:03.319009+00:00
finished_at2026-08-11T13:40:12.992030+00:00
source_last_modified2024-03-08T11:32:18.321280+01:00
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View the complete summary.json source
{
  "code": "SASDCK2",
  "status": "Published",
  "type_of_curve": "Other",
  "angular_unit": "1/A",
  "project": {
    "title": "2017 publication guidelines for structural modelling of small-angle scattering data from biomolecules in solution: an update.",
    "publication": {
      "title": "2017 publication guidelines for structural modelling of small-angle scattering data from biomolecules in solution: an update.",
      "author_list": "Trewhella J, Duff AP, Durand D, Gabel F, Guss JM, Hendrickson WA, Hura GL, Jacques DA, Kirby NM, Kwan AH, Pérez J, Pollack L, Ryan TM, Sali A, Schneidman-Duhovny D, Schwede T, Svergun DI, Sugiyama M, Tainer JA, Vachette P, Westbrook J, Whitten AE",
      "journal": "Acta Crystallogr D Struct Biol",
      "doi": "10.1107/S2059798317011597",
      "pmid": "28876235",
      "published_date": "2017 Sep 1"
    },
    "status": "released",
    "submitted_date": "2017-05-06",
    "released_date": "2017-08-22"
  },
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View the complete manifest.json source
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