查看完整 summary.json 原文
{
"code": "SASDB53",
"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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"country": "France",
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"long_name": "Dystrophin central domain repeats 1 to 3",
"short_name": "Dystrophin 338-668",
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"complex_state": false,
"deuteration": null,
"molecule_source": "biological",
"molecule_description": null
}
],
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"name": "20 mM Tris 150 mM NaCl 1 mM EDTA 2% glycerol",
"concentration_unit": "mM",
"comment": null,
"additive": "150 mM NaCl, 1 mM EDTA, 2% glycerol",
"concentration": 20.0,
"pka": null,
"ph": 7.5,
"deuteration": null
},
"purity_method": null,
"name": "Human dystrophin central domain repeats 1 to 3",
"ext_coefficient": null,
"contrast": null,
"specific_vol": null,
"dry_vol": null,
"absorbption": null,
"deuteration": null,
"mixture": null
},
"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
}
],
"concentration_method": null,
"concentration_unit": null,
"date": "2011-09-09",
"storage_temperature": 15.0,
"cell_temperature": null,
"exposure_time": 60.0,
"number_of_frames": 19,
"wavelength": 0.1,
"sample_detector_distance": 1.82,
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"s_min": 0.061,
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},
"fits": [
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"software": "SAXS-based",
"pdb_link": [],
"model_title": null,
"type_of_model": "atomic",
"software_version": "",
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"log": null,
"symmetry": "",
"comment": "",
"user": 97
}
],
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"software": null,
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}
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"pddf_software": "ATSAS GNOM",
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"description": null,
"experiment_description": "Synchrotron SAXS data were measured from solutions of Human Dystrophin central domain repeats 1 to 3 (amino acids 338-668) 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 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 (19 x 60 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.",
"tags": [],
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"porod_volume": 68.0,
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"intensities_log_log_plot": "SASDB53_datloglog_img.png",
"symmetry": null,
"last_modified": "2019-12-06T13:07:15.624532+01:00",
"bragg_peak": []
}查看完整 manifest.json 原文
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