查看完整 summary.json 原文
{
"code": "SASDBL7",
"status": "Published",
"type_of_curve": "Single concentration",
"angular_unit": "1/nm",
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"title": "Vaccinia Virus Immunomodulator A46: A Lipid and Protein-Binding Scaffold for Sequestering Host TIR-Domain Proteins.",
"publication": {
"title": "Vaccinia Virus Immunomodulator A46: A Lipid and Protein-Binding Scaffold for Sequestering Host TIR-Domain Proteins.",
"author_list": "Fedosyuk S, Bezerra GA, Radakovics K, Smith TK, Sammito M, Bobik N, Round A, Ten Eyck LF, Djinović-Carugo K, Usón I, Skern T",
"journal": "PLoS Pathog",
"doi": "10.1371/journal.ppat.1006079",
"pmid": "27973613",
"published_date": "2016 Dec"
},
"status": "released",
"submitted_date": "2016-11-06",
"released_date": "2016-11-23"
},
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"contributor": [
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"affiliation": [
{
"short_name": null,
"address": "Vienna, Austria",
"full_name": "Medical University of Vienna",
"webpage": "https://www.meduniwien.ac.at"
}
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"contributor_name": "Sofiya",
"contributor_surname": "Fedosyuk",
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"experiment_description": "Synchrotron SAXS data, I(s) vs s (s = 4π sin θ/λ, where 2θ is the scattering angle) were collected from a sample of the N-terminal domain of Vaccinia virus A46 protein (1-83) using continuous-flow size-exclusion chromatography SAXS (SEC-SAXS; Superdex 200 10/300 column) at the BM29 beam line on the ESRF storage ring (Grenoble, France). Data were collected using a Pilatus 1M detector at a sample-detector distance of 2.9 m and at a wavelength of λ = 0.09918 nm. The SEC mobile phase consisted of 20 mM Tris-HCl, 10 mM DTT, pH 8.5, (20°C) with a sample injection concentration of 15.5 mg/ml. Data obtained from solute-free eluates and SEC-elution peak were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted from the SEC-peak frames to produce the data displayed in this entry.",
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"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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