The following content comes directly from the SASBDB entry. Missing values are shown as “—”; SAXSdb does not infer undeclared units.
Every source field is expanded here, including empty values, list members and fields already shown above.
View the complete summary.json source
{
"code": "SASDBB3",
"status": "Published",
"type_of_curve": "Single concentration",
"angular_unit": "1/nm",
"project": {
"title": "Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions.",
"publication": {
"title": "Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions.",
"author_list": "Delalande O, Molza AE, Dos Santos Morais R, Chéron A, Pollet É, Raguenes-Nicol C, Tascon C, Giudice E, Guilbaud M, Nicolas A, Bondon A, Leturcq F, Férey N, Baaden M, Perez J, Roblin P, Piétri-Rouxel F, Hubert JF, Czjzek M, Le Rumeur E",
"journal": "J Biol Chem",
"doi": "10.1074/jbc.M117.809798",
"pmid": "29535188",
"published_date": "2018 May 4"
},
"status": "released",
"submitted_date": "2016-01-20",
"released_date": "2018-04-21"
},
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"deuteration": null,
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}
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"concentration_unit": "mM",
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"concentration": 20.0,
"pka": null,
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"deuteration": null
},
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"name": "Human dystrophin central domain single repeat 23",
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"absorbption": null,
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},
"contributor": [
{
"affiliation": [
{
"short_name": null,
"address": "Institut Génétique et Développement de Rennes, France",
"full_name": "Université de Rennes 1",
"webpage": ""
}
],
"contributor_name": "Elisabeth",
"contributor_surname": "Le Rumeur",
"orcid": null
}
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"date": "2011-10-07",
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"experiment_description": "Synchrotron SAXS data were measured from solutions of Human Dystrophin central domain repeat 23 (amino acids 2800-2939) in 20 mM Tris 150 mM NaCl, 1 mM EDTA, 2% glycerol buffer using size exclusion chromatography (SEC-SAXS) in combination with UV spectroscopy on the SWING beam line (SOLEIL, Saint-Aubin, France). The sample load concentration was 20 mg/mL. The scattering data, I(s) vs s (s = 4π sin θ/λ, where 2θ is the scattering angle) were collected through the corresponding SEC protein elution peak (30 x 1.5 s frames) as well as from the SEC column running buffer. The buffer scattering contributions were subtracted from each sample frame, which were then scaled and averaged to produce the SAXS profile displayed in this entry. The molecular weight estimate (MW) are derived from the Porod volume, Vp, where MW is approximately Vp/1.6. The SEC Rg and I(0) and UV trace are included in the additional files to this entry.",
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"symmetry": null,
"last_modified": "2019-12-06T13:07:15.624532+01:00",
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}View the complete manifest.json source
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