{
  "code": "SASDCQ7",
  "status": "Published",
  "type_of_curve": "Other",
  "angular_unit": "1/A",
  "project": {
    "title": "Structural Dynamics Control Allosteric Activation of Cytohesin Family Arf GTPase Exchange Factors.",
    "publication": {
      "title": "Structural Dynamics Control Allosteric Activation of Cytohesin Family Arf GTPase Exchange Factors.",
      "author_list": "Malaby AW, Das S, Chakravarthy S, Irving TC, Bilsel O, Lambright DG",
      "journal": "Structure",
      "doi": "10.1016/j.str.2017.11.019",
      "pmid": "29276036",
      "published_date": "2018 Jan 2"
    },
    "status": "released",
    "submitted_date": "2017-09-22",
    "released_date": "2018-01-02"
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        "resolution": null
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      "name": "Advanced Photon Source (APS), Argonne National Laboratory",
      "city": "Lemont, IL",
      "country": "USA",
      "beamline_name": "BioCAT 18ID",
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      "type_of_source": "X-ray synchrotron",
      "point_source": null,
      "line_collimation": null,
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      "line_collimation_integrationwidth": null,
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      "beam_profile_al": null
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          "organism": "Mus musculus",
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          "uniprot_range_last": null,
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          "molecular_type": "protein",
          "uniprot_sequence": null,
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      "buffer": {
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    "contributor": [
      {
        "affiliation": [
          {
            "short_name": "UMASS",
            "address": "Worcester, MA, USA",
            "full_name": "UMASS Medical School",
            "webpage": "https://www.umassmed.edu/"
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        "contributor_name": "David",
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    "concentration_unit": null,
    "date": "2013-11-15",
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  "experiment_description": "This experimental profile was derived from SEC-SAXS data collected at the BioCAT Sector 18-ID beamline at the Argonne National Laboratory Advanced Photon Source using a MAR 165 CCD detector.  The protein was equilibrated with a 1.2 molar excess of inositol 1,3,4,5-tetrakis phosphate (IP4), concentrated to 10 mg/ml, and injected in 0.1 ml onto a 3 ml Superdex-200 Increase column equilibrated with 20 mM Tris, pH 8.0, 150 mM NaCl, 2 mM MgCl2, 0.1% 2-mercaptoethanol, 5% glycerol, and 0.001 ml IP4.  SAXS data sets were acquired with 1 s exposures at 5 s intervals during elution at a flow rate of 0.25 ml/min.  Raw SAXS images were radially averaged on a log scale over the q range 0.00621-0.333 Å-1 and normalized by the incident beam intensity.  The protein scattering profile was reconstructed by singular value decomposition and linear combination (SVD-LC) as described in Malaby et al. (2015) Methods for analysis of size-exclusion chromatography-small angle X-ray scattering and reconstruction of protein scattering. J Appl Crystallogr 48: 1102-1113.",
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  "symmetry": null,
  "last_modified": "2020-08-28T15:28:09.410742+02:00",
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}