SASDWU6

Human anterior gradient protein 2 (AGR2)

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2025-10-27T12:08:22.283589+01:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Human anterior gradient protein 2 (AGR2)

Concentration— – 46.0 Buffer / pH20 mM Tris pH7.4, 150 mM NaCl, 1% glycerol, 0.2 mM TCEP / 7.4
Experimental temperature15.0 Facility / beamlineDiamond Light Source / B21
Wavelength0.09464 nmExposure1.0 s × 30

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Anterior gradient protein 2 homolog
View sequence
PQTLSRGWGDQLIWTQTYEEALYKSKTSNKPLMIIHHLDECPHSQALKKVFAENKEIQKLAEQFVLLNLVYETTDKHLSPDGQYVPRIMFVDPSLTVRADITGRYSNRLYAYEPADTALLLDNMKKALKLL
proteinHomo sapiensO9599441–171dimerMolecule count 215.122 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
12568[3]0.0045–0.34 1/AHas uncertainty columnMissing 00sasbdb/entries/u6/sasdwu6/source/SASDWU6.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)6.27—Å
i0Guinier0.177626—1/cm
i0P(r)0.1785—1/cm
mwExperimental24.4—kDa
mwPorod18.7—kDa
porod_volumePorod29.9—ų
rgGuinier1.9550.011Å
rgP(r)1.980.018Å

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 Tris pH7.4, 150 mM NaCl, 1% glycerol, 0.2 mM TCEPBuffer concentration—
pH7.4Additives—
Buffer descriptionThe buffer for SEC runs was the same as the sample buffer.
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2024-05-05Storage / measurement temperature15.0 / 15.0
Exposure time1.0Frames30
Wavelength0.09464Sample-to-detector distance3.6929
SourceX-ray synchrotronDetectorEiger 4M
Facility / beamlineDiamond Light Source / B21 · Didcot, UK
q range0.045 – 3.4Sample volume / flow rate35.0 / 0.06

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:169 field values
Field pathRaw value
codeSASDWU6
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleA structural basis for chaperone repression of stress signaling from the endoplasmic reticulum.
project.publication.titleA structural basis for chaperone repression of stress signaling from the endoplasmic reticulum.
project.publication.author_listNeidhardt L, Tung J, Kuchersky M, Milczarek J, Kargas V, Stott K, Rosenzweig R, Ron D, Yan Y
project.publication.journalMol Cell
project.publication.doi10.1016/j.molcel.2025.09.032
project.publication.pmid41135511
project.publication.published_date2025 Oct 23
project.statusreleased
project.submitted_date2025-01-24
project.released_date2025-10-23
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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_nameAnterior gradient protein 2 homolog
experiment.sample.molecule[0].short_nameAGR2
experiment.sample.molecule[0].sequencePQTLSRGWGDQLIWTQTYEEALYKSKTSNKPLMIIHHLDECPHSQALKKVFAENKEIQKLAEQFVLLNLVYETTDKHLSPDGQYVPRIMFVDPSLTVRADITGRYSNRLYAYEPADTALLLDNMKKALKLL
experiment.sample.molecule[0].organismHomo sapiens
experiment.sample.molecule[0].uniprot_codeO95994
experiment.sample.molecule[0].uniprot_range_first41
experiment.sample.molecule[0].uniprot_range_last171
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMEKIPVSAFLLLVALSYTLARDTTVKPGAKKDTKDSRPKLPQTLSRGWGDQLIWTQTYEE ALYKSKTSNKPLMIIHHLDECPHSQALKKVFAENKEIQKLAEQFVLLNLVYETTDKHLSP DGQYVPRIMFVDPSLTVRADITGRYSNRLYAYEPADTALLLDNMKKALKLLKTEL
experiment.sample.molecule[0].mw15.122
experiment.sample.molecule[0].total_mw30.244
experiment.sample.molecule[0].number_molecules2
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionRequired for MUC2 post-transcriptional synthesis and secretion.
experiment.sample.buffer.name20 mM Tris pH7.4, 150 mM NaCl, 1% glycerol, 0.2 mM TCEP
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentThe buffer for SEC runs was the same as the sample buffer.
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.nameHuman anterior gradient protein 2 (AGR2)
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_nameUniversity of Cambridge
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameYahui
experiment.contributor[0].contributor_surnameYan
experiment.contributor[0].orcidhttps://orcid.org/0000-0001-6934-9874
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2024-05-05
experiment.storage_temperature15.0
experiment.cell_temperature15.0
experiment.exposure_time1.0
experiment.number_of_frames30
experiment.wavelength0.09464
experiment.sample_detector_distance3.6929
experiment.concentration_minnull
experiment.concentration_max46.0
experiment.sample_volume35.0
experiment.flow_rate0.06
experiment.s_min0.045
experiment.s_max3.4
experiment.total_exposure_timenull
experiment.seccolumn13
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fits[0].models[0].commentnull
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fits[0].softwareMultiFoXS
fits[0].chi_square_value4.229369
fits[0].p_value0.0
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fits[0].fit_lognull
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fits[0].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of anterior gradient protein 2 (AGR2) in 20 mM Tris pH7.4, 150 mM NaCl, 1% glycerol, 0.2 mM TCEP, 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). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 35.00 μl sample at 46 mg/ml was injected at a 0.06 ml/min flow rate onto a GE Superdex 75 Increase 3.2/300 column at 15°C. 30 successive 1 second frames were collected through the sample elution peak (from a total of 600 frames collected throughout the entire SEC run). 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_mw24.4
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw18.7
porod_mw_errornull
pddf_i00.1785
pddf_i0_errornull
guinier_i00.177626
guinier_i0_errornull
pddf_rg1.98
pddf_rg_error0.018
guinier_rg1.955
guinier_rg_error0.011
pddf_dmax6.27
pddf_dmax_errornull
porod_volume29.9
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first224
guinier_point_last473
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDWU6_datloglog_img.png
symmetrynull
last_modified2025-10-27T12:08:22.283589+01:00
bragg_peak[]
manifest.json:34 field values
Field pathRaw value
codeSASDWU6
statussuccess
started_at2026-08-11T15:16:17.764370+00:00
finished_at2026-08-11T15:16:28.651993+00:00
source_last_modified2025-10-27T12:08:22.283589+01:00
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View the complete summary.json source
{
  "code": "SASDWU6",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "A structural basis for chaperone repression of stress signaling from the endoplasmic reticulum.",
    "publication": {
      "title": "A structural basis for chaperone repression of stress signaling from the endoplasmic reticulum.",
      "author_list": "Neidhardt L, Tung J, Kuchersky M, Milczarek J, Kargas V, Stott K, Rosenzweig R, Ron D, Yan Y",
      "journal": "Mol Cell",
      "doi": "10.1016/j.molcel.2025.09.032",
      "pmid": "41135511",
      "published_date": "2025 Oct 23"
    },
    "status": "released",
    "submitted_date": "2025-01-24",
    "released_date": "2025-10-23"
  },
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        "additive": null,
        "concentration": null,
        "pka": null,
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        "deuteration": null
      },
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      "name": "Human anterior gradient protein 2 (AGR2)",
      "ext_coefficient": null,
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      "absorbption": null,
      "deuteration": null,
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            "address": null,
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            "webpage": null
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View the complete manifest.json source
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