查看完整 summary.json 原文
{
"code": "SASDDA2",
"status": "Published",
"type_of_curve": "Single concentration",
"angular_unit": "1/nm",
"project": {
"title": "Functionally specific binding regions of microtubule-associated protein 2c exhibit distinct conformations and dynamics.",
"publication": {
"title": "Functionally specific binding regions of microtubule-associated protein 2c exhibit distinct conformations and dynamics.",
"author_list": "Melková K, Zapletal V, Jansen S, Nomilner E, Zachrdla M, Hritz J, Nováček J, Zweckstetter M, Jensen MR, Blackledge M, Žídek L",
"journal": "J Biol Chem",
"doi": "10.1074/jbc.RA118.001769",
"pmid": "29925592",
"published_date": "2018 Aug 24"
},
"status": "released",
"submitted_date": "2017-12-21",
"released_date": "2018-06-19"
},
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"name": "Pilatus 1M",
"resolution": 172.0
},
"name": "ESRF",
"city": "Grenoble",
"country": "France",
"beamline_name": "BM29",
"beam_geometry": "",
"type_of_source": "X-ray synchrotron",
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{
"long_name": "Microtubule-associated protein 2, isoform 3",
"short_name": "MAP2c",
"sequence": "MADERKDEGKAPHWTSASLTEAAAHPHSPEMKDQGGSGEGLSRSANGFPYREEEEGAFGEHGSQGTYSDTKENGINGELTSADRETAEEVSARIVQVVTAEAVAVLKGEQEKEAQHKDQPAALPLAAEETVNLPPSPPPSPASEQTAALEEATSGESAQAPSAFKQAKDKVTDGITKSPEKRSSLPRPSSILPPRRGVSGDREENSFSLNSSISSARRTTRSEPIRRAGKSGTSTPTTPGSTAITPGTPPSYSSRTPGTPGTPSYPRTPGTPKSGILVPSEKKVAIIRTPPKSPATPKQLRLINQPLPDLKNVKSKIGSTDNIKYQPKGGQVQIVTKKIDLSHVTSKCGSLKNIRHRPGGGRVKIESVKLDFKEKAQAKVGSLDNAHHVPGGGNVKIDSQKLNFREHAKARVDHGAEIITQSPSRSSVASPRRLSNVSSSGSINLLESPQLATLAEDVTAALAKQGL",
"organism": "Rattus norvegicus",
"uniprot_code": "P15146",
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"oligomerization": "monomer",
"molecular_type": "protein",
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"number_molecules": 1,
"complex_state": false,
"deuteration": null,
"molecule_source": "biological",
"molecule_description": null
}
],
"buffer": {
"name": "50 mM MOPS, 150 mM NaCl, 0.03% NaN3",
"concentration_unit": null,
"comment": "aka: MOPS map2c buffer",
"additive": null,
"concentration": null,
"pka": null,
"ph": 6.9,
"deuteration": null
},
"purity_method": null,
"name": "Phosphorylated Microtubule associated protein MAP2c (isoform 3); 13.6 mg/ml",
"ext_coefficient": null,
"contrast": null,
"specific_vol": null,
"dry_vol": null,
"absorbption": null,
"deuteration": null,
"mixture": null
},
"contributor": [
{
"affiliation": [
{
"short_name": "MUNI",
"address": "Brno, Czech Republic",
"full_name": "Masaryk University; \tResearch group Structure and Dynamics of Proteins.",
"webpage": "https://www.muni.cz/"
}
],
"contributor_name": "Vojtech",
"contributor_surname": "Zapletal",
"orcid": null
}
],
"concentration_method": null,
"concentration_unit": null,
"date": "2017-04-21",
"storage_temperature": 20.0,
"cell_temperature": 20.0,
"exposure_time": 1.0,
"number_of_frames": 10,
"wavelength": 0.099,
"sample_detector_distance": null,
"concentration_min": null,
"concentration_max": 13.6,
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"flow_rate": null,
"s_min": 0.031,
"s_max": 4.944,
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},
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"description": null,
"experiment_description": "Synchrotron SAXS data from solutions of phosphorylated microtubule associated protein MAP2c (isoform 3) in 50 mM MOPS, 150 mM NaCl, 0,03% NaN3, pH 6.9 were collected on the BM29 beam line at the ESRF (Grenoble, France) using a Pilatus 1M detector at an X-ray wavelength, λ, of 0.099 nm (I(s) vs s, where s = 4πsinθ/λ and 2θ is the scattering angle). One solute concentration of 13.60 mg/ml was measured at 20°C. A total of 10 successive 1 s data 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 data were scaled for protein concentration.",
"tags": [
"idp"
],
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"estimated_volume": null,
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"pddf_point_first": null,
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"i0_calibration_standard_data": null,
"intensities_log_log_plot": "SASDDA2_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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