查看完整 summary.json 原文
{
"code": "SASDBX9",
"status": "Published",
"type_of_curve": "Single concentration",
"angular_unit": "1/A",
"project": {
"title": "Molecular Architecture of the Major Membrane Ring Component of the Nuclear Pore Complex.",
"publication": {
"title": "Molecular Architecture of the Major Membrane Ring Component of the Nuclear Pore Complex.",
"author_list": "Upla P, Kim SJ, Sampathkumar P, Dutta K, Cahill SM, Chemmama IE, Williams R, Bonanno JB, Rice WJ, Stokes DL, Cowburn D, Almo SC, Sali A, Rout MP, Fernandez-Martinez J",
"journal": "Structure",
"doi": "10.1016/j.str.2017.01.006",
"pmid": "28162953",
"published_date": "2017 Mar 7"
},
"status": "released",
"submitted_date": "2017-01-23",
"released_date": "2017-02-16"
},
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},
"name": "Stanford Synchrotron Radiation Lightsource (SSRL)",
"city": "Menlo Park, CA",
"country": "USA",
"beamline_name": "BL4-2",
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{
"long_name": "Nucleoporin POM152",
"short_name": null,
"sequence": "EKPKFAIQDNHHITKVTENLFSKEEVCQGMEGTVDLALFGSPPFILEYDLMAPNGHISTKKIQVATKYASLKLPNQIPGEYITTIKAIFDGNYGESDIHFREEGHHHHHH",
"organism": "Saccharomyces cerevisiae",
"uniprot_code": "P39685",
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"oligomerization": "monomer",
"molecular_type": "protein",
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"mw": 12.479,
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"number_molecules": 1,
"complex_state": false,
"deuteration": null,
"molecule_source": "biological",
"molecule_description": null
}
],
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"concentration_unit": null,
"comment": null,
"additive": null,
"concentration": null,
"pka": null,
"ph": 7.5,
"deuteration": null
},
"purity_method": null,
"name": "Immunoglobulin domain 6 of Nucleoporin Pom152 (Pom152 Ig-6: amino acids 919-1020)",
"ext_coefficient": null,
"contrast": null,
"specific_vol": null,
"dry_vol": null,
"absorbption": null,
"deuteration": null,
"mixture": null
},
"contributor": [
{
"affiliation": [
{
"short_name": "UCSF",
"address": "San Francisco, CA, USA",
"full_name": "University of California, San Francisco (UCSF)",
"webpage": "https://www.ucsf.edu/"
}
],
"contributor_name": "Seung Joong",
"contributor_surname": "Kim",
"orcid": null
}
],
"concentration_method": null,
"concentration_unit": null,
"date": "2015-04-12",
"storage_temperature": 15.0,
"cell_temperature": 15.0,
"exposure_time": 1.0,
"number_of_frames": 20,
"wavelength": 0.098,
"sample_detector_distance": 1.7,
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},
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"log": null,
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}
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"fit_unit": "1/A",
"fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDBX9_fit1_fit_img.png",
"software": "DAMMIN",
"chi_square_value": 2.863,
"p_value": 0.0,
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"fit_data": "https://www.sasbdb.org/media/fitting_files/SASDBX9_fit1.fir",
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}
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"i0_calibration_standard": null,
"description": "Guinier Rg and I_0 were calculated using AutoRg.\r\n\r\nMW was estimated using SAXSMOW.",
"experiment_description": "Synchrotron SAXS data from solutions of Immunoglobulin domain 6 of Nucleoporin Pom152 (Pom152 Ig-6: amino acids 919-1020) in 10mM HEPES, 150mM NaCl, 10%(v/v) glycerol, 5mM DTT, pH 7.5 were collected on the BL4-2 beam line at the Stanford Synchrotron Radiation Lightsource (SSRL) (Stanford, CA, USA) using a Rayonix MX225-HE detector at a sample-detector distance of 1.7 m and at a wavelength of λ = 0.098 nm (I(s) vs s, where s = 4πsinθ/λ and 2θ is the scattering angle). Solute concentrations ranging between 1 and 1 mg/ml were measured at 15°C. 20 successive 1 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 and the different curves were scaled for protein concentration.",
"tags": [],
"intensity_unit": null,
"experimental_mw": 12.5,
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"pddf_i0": 198.7,
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"pddf_dmax": 7.93,
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"porod_volume": 56.68,
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"estimated_volume": null,
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"guinier_point_first": 8,
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"i0_calibration_standard_data": null,
"intensities_log_log_plot": "SASDBX9_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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