SASDUW6

Alarmin release inhibitor (HpARI2), full-length

Data type: SASBDB experimental data Status: Published Curve type: Single concentration Last updated: 2024-06-23T14:27:49.590707+02:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Alarmin release inhibitor (HpARI2), full-length

Concentration— – 8.0 Buffer / pH137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 5% glycerol / 7.2
Experimental temperature15.0 Facility / beamlineDiamond Light Source / B21
Wavelength0.09464 nmExposure3.0 s × 600

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Alarmin release inhibitor (Δ1-62)
View sequence
AGQRCRFTDVERDKGYTGMLLKGRLRKTAGNGRTVELICGRGNHNYTCESGVLKESSPRQARCGCKGILEMLFDMPKEERPSPMYDSVTYDPTPNTPTTVGKDGIWNGVDYRNGSTVKPYCDTGPVINGSSKAVCVSGKWVPTLGVCPKMCSIGSLKENGKFVDVTATTKGDELNPPPREQTLIPIVRKVDKDKVQHGVKVVALCKAEDSTTAAEGVQEFECDNGKWKPEPVPCPEPEA
proteinHeligmosomoides polygyrusA0A3P7XL1863–297monomerMolecule count 125.998 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
12568[3]0.0045–0.34 1/AHas uncertainty columnMissing 071sasbdb/entries/w6/sasduw6/source/SASDUW6.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)9.86—Å
i0Guinier0.042546—1/cm
i0P(r)0.04296—1/cm
mwExperimental26.0—kDa
mwGuinier I(0)21.78—kDa
mwPorod19.4—kDa
porod_volumePorod31.0—ų
rgGuinier2.6320.041Å
rgP(r)2.76—Å

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 name137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 5% glycerolBuffer concentration—
pH7.2Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2024-02-09Storage / measurement temperature15.0 / 15.0
Exposure time3.0Frames600
Wavelength0.09464Sample-to-detector distance3.7025
SourceX-ray synchrotronDetectorEiger 4M
Facility / beamlineDiamond Light Source / B21 · Didcot, UK
q range0.045 – 3.4Sample 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:179 field values
Field pathRaw value
codeSASDUW6
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleStructural basis for IL-33 recognition and its antagonism by the helminth effector protein HpARI2.
project.publication.titleStructural basis for IL-33 recognition and its antagonism by the helminth effector protein HpARI2.
project.publication.author_listJamwal A, Colomb F, McSorley HJ, Higgins MK
project.publication.journalNat Commun
project.publication.doi10.1038/s41467-024-49550-0
project.publication.pmid38890291
project.publication.published_date2024 Jun 19
project.statusreleased
project.submitted_date2024-04-10
project.released_date2024-04-25
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experiment.instrument.detector.typenull
experiment.instrument.detector.nameEiger 4M
experiment.instrument.detector.resolution75.0
experiment.instrument.nameDiamond Light Source
experiment.instrument.cityDidcot
experiment.instrument.countryUK
experiment.instrument.beamline_nameB21
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_nameAlarmin release inhibitor (Δ1-62)
experiment.sample.molecule[0].short_nameHpARI2
experiment.sample.molecule[0].sequenceAGQRCRFTDVERDKGYTGMLLKGRLRKTAGNGRTVELICGRGNHNYTCESGVLKESSPRQARCGCKGILEMLFDMPKEERPSPMYDSVTYDPTPNTPTTVGKDGIWNGVDYRNGSTVKPYCDTGPVINGSSKAVCVSGKWVPTLGVCPKMCSIGSLKENGKFVDVTATTKGDELNPPPREQTLIPIVRKVDKDKVQHGVKVVALCKAEDSTTAAEGVQEFECDNGKWKPEPVPCPEPEA
experiment.sample.molecule[0].organismHeligmosomoides polygyrus
experiment.sample.molecule[0].uniprot_codeA0A3P7XL18
experiment.sample.molecule[0].uniprot_range_first63
experiment.sample.molecule[0].uniprot_range_last297
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMDIIGQVYCFTGAPHTITCLLREQFINWYIKYKRSENYPAFRELVVMYRLFLALGFLTFI NAAGQRCRFTDVERDKGYTGMLLKGRLRKTAGNGRTVELICGRGNHNYTCESGVLKESSP RQARCGCKGILEMLFDMPKEERPSPMYDSVTYDPTPNTPTTVGKDGIWNGVDYRNGSTVK PYCDTGPVINGSSKAVCVSGKWVPTLGVCPKMCSIGSLKENGKFVDVTATTKGDELNPPP REQTLIPIVRKVDKDKVQHGVKVVALCKAEDSTTAAEGVQEFECDNGKWKPEPVPCP
experiment.sample.molecule[0].mw25.998
experiment.sample.molecule[0].total_mw25.998
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_descriptionThe protein construct used for SAXS contains an additional four non-native amino acids at the C-terminus (EPEA).
experiment.sample.buffer.name137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 5% glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.2
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameAlarmin release inhibitor (HpARI2), full-length
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].addressnull
experiment.contributor[0].affiliation[0].full_nameDepartment of Biochemistry, University of Oxford
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameMatt
experiment.contributor[0].contributor_surnameHiggins
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2024-02-09
experiment.storage_temperature15.0
experiment.cell_temperature15.0
experiment.exposure_time3.0
experiment.number_of_frames600
experiment.wavelength0.09464
experiment.sample_detector_distance3.7025
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experiment.concentration_max8.0
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.045
experiment.s_max3.4
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].p_value0.2384
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fits[1].p_value0.0097
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fits[1].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of alarmin release inhibitor in 137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 5% glycerol, pH 7.2 were collected on the B21 beam line at the Diamond Light Source (Didcot, UK) using a Eiger 4M detector at a sample-detector distance of 3.7 m and at a wavelength of λ = 0.09464 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 8.00 mg/ml was measured at 15°C. 600 successive 3 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_unit1/cm
experimental_mw26.0
experimental_mw_errornull
guinier_i0_mw21.78
guinier_i0_mw_errornull
porod_mw19.4
porod_mw_errornull
pddf_i00.04296
pddf_i0_errornull
guinier_i00.042546
guinier_i0_errornull
pddf_rg2.76
pddf_rg_errornull
guinier_rg2.632
guinier_rg_error0.041
pddf_dmax9.86
pddf_dmax_errornull
porod_volume31.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first54
guinier_point_last343
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDUW6_datloglog_img.png
symmetrynull
last_modified2024-06-23T14:27:49.590707+02:00
bragg_peak[]
manifest.json:34 field values
Field pathRaw value
codeSASDUW6
statussuccess
started_at2026-08-11T15:17:38.865873+00:00
finished_at2026-08-11T15:17:47.960253+00:00
source_last_modified2024-06-23T14:27:49.590707+02:00
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View the complete summary.json source
{
  "code": "SASDUW6",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Structural basis for IL-33 recognition and its antagonism by the helminth effector protein HpARI2.",
    "publication": {
      "title": "Structural basis for IL-33 recognition and its antagonism by the helminth effector protein HpARI2.",
      "author_list": "Jamwal A, Colomb F, McSorley HJ, Higgins MK",
      "journal": "Nat Commun",
      "doi": "10.1038/s41467-024-49550-0",
      "pmid": "38890291",
      "published_date": "2024 Jun 19"
    },
    "status": "released",
    "submitted_date": "2024-04-10",
    "released_date": "2024-04-25"
  },
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      "point_source": null,
      "line_collimation": null,
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    "sample": {
      "molecule": [
        {
          "long_name": "Alarmin release inhibitor (Δ1-62)",
          "short_name": "HpARI2",
          "sequence": "AGQRCRFTDVERDKGYTGMLLKGRLRKTAGNGRTVELICGRGNHNYTCESGVLKESSPRQARCGCKGILEMLFDMPKEERPSPMYDSVTYDPTPNTPTTVGKDGIWNGVDYRNGSTVKPYCDTGPVINGSSKAVCVSGKWVPTLGVCPKMCSIGSLKENGKFVDVTATTKGDELNPPPREQTLIPIVRKVDKDKVQHGVKVVALCKAEDSTTAAEGVQEFECDNGKWKPEPVPCPEPEA",
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          "uniprot_code": "A0A3P7XL18",
          "uniprot_range_first": 63,
          "uniprot_range_last": 297,
          "oligomerization": "monomer",
          "molecular_type": "protein",
          "uniprot_sequence": "MDIIGQVYCFTGAPHTITCLLREQFINWYIKYKRSENYPAFRELVVMYRLFLALGFLTFI\nNAAGQRCRFTDVERDKGYTGMLLKGRLRKTAGNGRTVELICGRGNHNYTCESGVLKESSP\nRQARCGCKGILEMLFDMPKEERPSPMYDSVTYDPTPNTPTTVGKDGIWNGVDYRNGSTVK\nPYCDTGPVINGSSKAVCVSGKWVPTLGVCPKMCSIGSLKENGKFVDVTATTKGDELNPPP\nREQTLIPIVRKVDKDKVQHGVKVVALCKAEDSTTAAEGVQEFECDNGKWKPEPVPCP",
          "mw": 25.998,
          "total_mw": 25.998,
          "number_molecules": 1,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": "The protein construct used for SAXS contains an additional four non-native amino acids at the C-terminus (EPEA)."
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View the complete manifest.json source
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