SASDE96

Aldehyde dehydrogenase 12 from Zea mays Extrapolated to Infinite Dilution

Data type: SASBDB experimental data Status: Published Curve type: Extrapolated to infinite dilution Last updated: 2019-12-06T13:07:15.624532+01:00

This is the background subtracted experimental SAXS data extrapolated to infinite dilution. The original experiment consisted of static SAXS samples collected at 3 protein concentrations in the range of 0.9 - 2.6 mg/mL. The data were extrapolated to infinite dilution to account for sample aggregation in the two higher concentration samples. The corresponding model fits of the tetramer (top) and dimer (bottom) demonstrate that the dimer does not fit the SAXS data.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Aldehyde dehydrogenase 12 from Zea mays Extrapolated to Infinite Dilution

Concentration— – — Buffer / pH50 mM Tris-HCl, 50 mM NaCl, 0.5 mM TCEP, and 5% (v/v) glycerol / 7.8
Experimental temperature10.0 Facility / beamlineAdvanced Light Source (ALS) / 12.3.1 (SIBYLS)
Wavelength0.127 nmExposure0.3 s × 33

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Aldehyde dehydrogenase 12
View sequence
>ZMALDH12MGSSHHHHHHSQDPAPFACVSRWLHTPSFATVSPQEVSGSSPAEVQNFVQGSWTASANWNWIVDPLNGDKFIKVAEVQGTEIKSFMESLSKCPKHGLHNPLKAPERYLMYGDISAKAAHMLGQPTVLDFFAKLIQRVSPKSYQQALAEVQVSQKFLENFCGDQVRFLARSFAVPGNHLGQRSNGYRWPYGPVAIITPFNFPLEIPLLQLMGALYMGNKPVLKVDSKVSIVMEQMIRLLHDCGLPAEDMDFINSDGAVMNKLLLEANPKMTLFTGSSRVAEKLAADLKGRVKLEDAGFDWKILGPDVQEVDYVAWVCDQDAYACSGQKCSAQSVLFMHKNWSSSGLLEKMKKLSERRKLEDLTIGPVLTVTTEAMIEHMNNLLKIRGSKVLFGGEPLANHSIPKIYGAMKPTAVFVPLEEILKSGNFELVTKEIFGPFQVVTEYSEDQLELVLEACERMNAHLTAAIVSNDPLFLQDVLGRSVNGTTYAGIRARTTGAPQNHWFGPAGDPRGAGIGTPEAIKLVWSCHREIIYDVGPVPESWALPSAT
proteinZea maysA0A2H4PMI317–549tetramerMolecule count 460.397 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
1954[3]0.013075–0.592387 1/AHas uncertainty columnMissing 0187sasbdb/entries/96/sasde96/source/SASDE96.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)14.43—Å
i0Guinier92.630.5arbitrary
i0P(r)90.51—arbitrary
mwExperimental249.8—kDa
mwPorod219.0—kDa
porod_volumePorod351.0—ų
rgGuinier4.140.03Å
rgP(r)4.02—Å

These values are reported by SASBDB; SAXSdb did not recalculate them from the experimental curve.

▼

3. Source Fits and Models Source Fits & Models

Fit 2 · FoXS

χ²: 57.378343CorMap p: 0.0Unit: 1/A

Fit of the experimental data to an AllosMod dimer model.

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—mixAllosMod —120.8—Model Image
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4. Source File Index Source Files

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5. Experiment Description and Publication Experiment & Publication

▼

6. Complete Source Record Complete Source Record

The following content comes directly from the SASBDB entry. Missing values are shown as “—”; SAXSdb does not infer undeclared units.

Open the original SASBDB entry

Buffer and Sample Properties

Buffer name50 mM Tris-HCl, 50 mM NaCl, 0.5 mM TCEP, and 5% (v/v) glycerolBuffer concentration—
pH7.8Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2016-12-06Storage / measurement temperature4.0 / 10.0
Exposure time0.3Frames33
Wavelength0.127Sample-to-detector distance1.5
SourceX-ray synchrotronDetectorPilatus3 X 2M
Facility / beamlineAdvanced Light Source (ALS) / 12.3.1 (SIBYLS) · Berkeley, CA, USA
q range0.131 – 5.924Sample volume / flow rate— / —

Original SASBDB Plots

Experimental I(q)
Experimental I(q)
Experimental I(q), log-log
Experimental I(q), log-log
Guinier plot
Guinier plot
Kratky plot
Kratky plot
P(r) plot
P(r) plot

Downloadable Files

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All source fields (unfiltered)

Every source field is expanded here, including empty values, list members and fields already shown above.

summary.json:179 field values
Field pathRaw value
codeSASDE96
statusPublished
type_of_curveExtrapolated to infinite dilution
angular_unit1/A
project.titleStructural and Biochemical Characterization of Aldehyde Dehydrogenase 12, the Last Enzyme of Proline Catabolism in Plants.
project.publication.titleStructural and Biochemical Characterization of Aldehyde Dehydrogenase 12, the Last Enzyme of Proline Catabolism in Plants.
project.publication.author_listKorasick DA, Končitíková R, Kopečná M, Hájková E, Vigouroux A, Moréra S, Becker DF, Šebela M, Tanner JJ, Kopečný D
project.publication.journalJ Mol Biol
project.publication.doi10.1016/j.jmb.2018.12.010
project.publication.pmid30580036
project.publication.published_date2018 Dec 20
project.statusreleased
project.submitted_date2018-10-09
project.released_date2018-12-27
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experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus3 X 2M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameAdvanced Light Source (ALS)
experiment.instrument.cityBerkeley, CA
experiment.instrument.countryUSA
experiment.instrument.beamline_name12.3.1 (SIBYLS)
experiment.instrument.beam_geometry
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
experiment.instrument.line_collimationnull
experiment.instrument.sample_path_lengthnull
experiment.instrument.line_collimation_slitlengthnull
experiment.instrument.line_collimation_integrationwidthnull
experiment.instrument.xray_energynull
experiment.instrument.beam_profile_ahnull
experiment.instrument.beam_profile_alnull
experiment.sample.molecule[0].long_nameAldehyde dehydrogenase 12
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequence>ZmALDH12 MGSSHHHHHHSQDPAPFACVSRWLHTPSFATVSPQEVSGSSPAEVQNFVQGSWTASANWNWIVDPLNGDKFIKVAEVQGTEIKSFMESLSKCPKHGLHNPLKAPERYLMYGDISAKAAHMLGQPTVLDFFAKLIQRVSPKSYQQALAEVQVSQKFLENFCGDQVRFLARSFAVPGNHLGQRSNGYRWPYGPVAIITPFNFPLEIPLLQLMGALYMGNKPVLKVDSKVSIVMEQMIRLLHDCGLPAEDMDFINSDGAVMNKLLLEANPKMTLFTGSSRVAEKLAADLKGRVKLEDAGFDWKILGPDVQEVDYVAWVCDQDAYACSGQKCSAQSVLFMHKNWSSSGLLEKMKKLSERRKLEDLTIGPVLTVTTEAMIEHMNNLLKIRGSKVLFGGEPLANHSIPKIYGAMKPTAVFVPLEEILKSGNFELVTKEIFGPFQVVTEYSEDQLELVLEACERMNAHLTAAIVSNDPLFLQDVLGRSVNGTTYAGIRARTTGAPQNHWFGPAGDPRGAGIGTPEAIKLVWSCHREIIYDVGPVPESWALPSAT
experiment.sample.molecule[0].organismZea mays
experiment.sample.molecule[0].uniprot_codeA0A2H4PMI3
experiment.sample.molecule[0].uniprot_range_first17
experiment.sample.molecule[0].uniprot_range_last549
experiment.sample.molecule[0].oligomerizationtetramer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMSRLLSRQHLAAVRRSAPFACVSRWLHTPSFATVSPQEVSGSSPAEVQNFVQGSWTASAN WNWIVDPLNGDKFIKVAEVQGTEIKSFMESLSKCPKHGLHNPLKAPERYLMYGDISAKAA HMLGQPTVLDFFAKLIQRVSPKSYQQALAEVQVSQKFLENFCGDQVRFLARSFAVPGNHL GQRSNGYRWPYGPVAIITPFNFPLEIPLLQLMGALYMGNKPVLKVDSKVSIVMEQMIRLL HDCGLPAEDMDFINSDGAVMNKLLLEANPKMTLFTGSSRVAEKLAADLKGRVKLEDAGFD WKILGPDVQEVDYVAWVCDQDAYACSGQKCSAQSVLFMHKNWSSSGLLEKMKKLSERRKL EDLTIGPVLTVTTEAMIEHMNNLLKIRGSKVLFGGEPLANHSIPKIYGAMKPTAVFVPLE EILKSGNFELVTKEIFGPFQVVTEYSEDQLELVLEACERMNAHLTAAIVSNDPLFLQDVL GRSVNGTTYAGIRARTTGAPQNHWFGPAGDPRGAGIGTPEAIKLVWSCHREIIYDVGPVP ESWALPSAT
experiment.sample.molecule[0].mw60.397
experiment.sample.molecule[0].total_mw241.588
experiment.sample.molecule[0].number_molecules4
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionnull
experiment.sample.buffer.name50 mM Tris-HCl, 50 mM NaCl, 0.5 mM TCEP, and 5% (v/v) glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.8
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameAldehyde dehydrogenase 12 from Zea mays Extrapolated to Infinite Dilution
experiment.sample.ext_coefficientnull
experiment.sample.contrastnull
experiment.sample.specific_volnull
experiment.sample.dry_volnull
experiment.sample.absorbptionnull
experiment.sample.deuterationnull
experiment.sample.mixturenull
experiment.contributor[0].affiliation[0].short_nameMizzou
experiment.contributor[0].affiliation[0].addressColumbia, MO, USA
experiment.contributor[0].affiliation[0].full_nameUniversity of Missouri-Columbia
experiment.contributor[0].affiliation[0].webpagehttp://missouri.edu/
experiment.contributor[0].contributor_nameDavid
experiment.contributor[0].contributor_surnameKorasick
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2016-12-06
experiment.storage_temperature4.0
experiment.cell_temperature10.0
experiment.exposure_time0.3
experiment.number_of_frames33
experiment.wavelength0.127
experiment.sample_detector_distance1.5
experiment.concentration_minnull
experiment.concentration_maxnull
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.131
experiment.s_max5.924
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].p_value1.2e-05
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fits[1].softwareFoXS
fits[1].chi_square_value57.378343
fits[1].p_value0.0
fits[1].fit_residual_plotdimer4_zc_001_133_133_13_fitresiduals_img.png
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fits[1].fit_lognull
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fits[1].descriptionFit of the experimental data to an AllosMod dimer model.
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionThis is the background subtracted experimental SAXS data extrapolated to infinite dilution. The original experiment consisted of static SAXS samples collected at 3 protein concentrations in the range of 0.9 - 2.6 mg/mL. The data were extrapolated to infinite dilution to account for sample aggregation in the two higher concentration samples. The corresponding model fits of the tetramer (top) and dimer (bottom) demonstrate that the dimer does not fit the SAXS data.
experiment_descriptionSynchrotron SAXS data from solutions of aldehyde dehydrogenase in 50 mM Tris-HCl, 50 mM NaCl, 0.5 mM TCEP, and 5% (v/v) glycerol, pH 7.8 were collected on the 12.3.1 (SIBYLS) beam line at the Advanced Light Source (ALS, Berkeley, CA, USA) using a Pilatus3 X 2M detector at a sample-detector distance of 1.5 m and at a wavelength of λ = 0.127 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). 33 successive 0.300 second frames were collected at a sample temperature of 10°C. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted. The low angle data collected at lower concentrations were extrapolated to infinite dilution and merged with the higher concentration data to yield the final composite scattering curve.
tags[]
intensity_unitarbitrary
experimental_mw249.8
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw219.0
porod_mw_errornull
pddf_i090.51
pddf_i0_errornull
guinier_i092.63
guinier_i0_error0.5
pddf_rg4.02
pddf_rg_errornull
guinier_rg4.14
guinier_rg_error0.03
pddf_dmax14.43
pddf_dmax_errornull
porod_volume351.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last31
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDE96_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDE96
statussuccess
started_at2026-08-11T15:04:19.840260+00:00
finished_at2026-08-11T15:04:30.761045+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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View the complete summary.json source
{
  "code": "SASDE96",
  "status": "Published",
  "type_of_curve": "Extrapolated to infinite dilution",
  "angular_unit": "1/A",
  "project": {
    "title": "Structural and Biochemical Characterization of Aldehyde Dehydrogenase 12, the Last Enzyme of Proline Catabolism in Plants.",
    "publication": {
      "title": "Structural and Biochemical Characterization of Aldehyde Dehydrogenase 12, the Last Enzyme of Proline Catabolism in Plants.",
      "author_list": "Korasick DA, Končitíková R, Kopečná M, Hájková E, Vigouroux A, Moréra S, Becker DF, Šebela M, Tanner JJ, Kopečný D",
      "journal": "J Mol Biol",
      "doi": "10.1016/j.jmb.2018.12.010",
      "pmid": "30580036",
      "published_date": "2018 Dec 20"
    },
    "status": "released",
    "submitted_date": "2018-10-09",
    "released_date": "2018-12-27"
  },
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View the complete manifest.json source
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