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": "SASDCK3",
"status": "Published",
"type_of_curve": "Single concentration",
"angular_unit": "1/A",
"project": {
"title": "High-resolution structure of the alcohol dehydrogenase domain of the bifunctional bacterial enzyme AdhE.",
"publication": {
"title": "High-resolution structure of the alcohol dehydrogenase domain of the bifunctional bacterial enzyme AdhE.",
"author_list": "Azmi L, Bragginton EC, Cadby IT, Byron O, Roe AJ, Lovering AL, Gabrielsen M",
"journal": "Acta Crystallogr F Struct Biol Commun",
"doi": "10.1107/S2053230X20010237",
"pmid": "32880589",
"published_date": "2020 Sep 1"
},
"status": "released",
"submitted_date": "2017-05-11",
"released_date": "2017-12-12"
},
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{
"long_name": "Aldehyde-alcohol dehydrogenase",
"short_name": "AdhE",
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"organism": "Escherichia coli O157:H7",
"uniprot_code": "P0A9Q8",
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"oligomerization": "monomer",
"molecular_type": "protein",
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}
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"name": "Aldehyde dehydrogenase",
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"contributor": [
{
"affiliation": [
{
"short_name": null,
"address": "Glasgow, Scotland, UK",
"full_name": "University of Glasgow",
"webpage": "http://www.gla.ac.uk/"
}
],
"contributor_name": "Liyana",
"contributor_surname": "Azmi",
"orcid": null
}
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"date": "2017-01-30",
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"comment": "",
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"fit_residual_plot": "SASDCK3_fit2_fitresiduals_img.png",
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"description": "Aldehyde dehydrogenase (AldDH) is the N-terminal domain of the bifunctional alcohol/aldehyde dehydrogenase (AdhE; SASBDB entry SASDC72) spanning amino acids 1-445 of the full-length protein. SAXS data were measured from a protein construct that included a C-terminal 6 x histidine affinity chromatography tag. The buffer subtraction was performed using Scatter. Subsequent analysis was performed using PRIMUS (ATSAS 2.7.1).",
"experiment_description": "Synchrotron SAXS data from solutions of aldehyde dehydrogenase in 30 mM HEPES, 150 mM NaCl, 5% (v/v) glycerol, pH 7.5 were collected on the B21 camera at the Diamond Light Source (Oxfordshire, UK) using a Pilatus 2M detector at a sample-detector distance of 4.0 m and at a wavelength of λ = 0.1 nm ((Is) vs s, where s = 4πsinθ/λ and 2θ is the scattering angle). One solute concentration of 2.00 mg/ml was measured at 4°C. 18 successive 1 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged and the scattering of the solvent-blank was subtracted to obtain the SAXS profile displayed in this entry.",
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"intensities_log_log_plot": "SASDCK3_datloglog_img.png",
"symmetry": null,
"last_modified": "2021-01-04T12:08:43.437315+01:00",
"bragg_peak": []
}
View the complete manifest.json source
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