SASDGA5

The C-terminal cell-surface signaling domain of the Pseudomonas capeferrum anti-sigma regulator PupR

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2020-03-03T14:59:07.808703+01:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · The C-terminal cell-surface signaling domain of the Pseudomonas capeferrum anti-sigma regulator PupR

Concentration— – 9.6 Buffer / pH25 mM HEPES 400 mM LiCl 10% v/v glycerol / 7.5
Experimental temperature25.0 Facility / beamlineAdvanced Photon Source (APS), Argonne National Laboratory / BioCAT 18ID
Wavelength0.103 nmExposure— s × —

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
PupR protein
View sequence
GAMGQDWRADYHSRIGEQRRLTLADGTQVQLNTDSALNVAFDQQARRLRLVRGEMLITRPALADSRPLWVDTEHGRLESTLAQFNVRLHGQHTQATVYQGSVALQPALHAYPPILLGAGEQASFNQQGLLARQAVAAVAPAWSQGMLVAQGQPLAAFIEDLARYRRGHLACDPALAGLRVSGTFPLENTDKIIAAVAETLQLEVQHFTRYWVTLKPRMA
proteinPseudomonas putidaQ52209110–324monomerMolecule count 124.124 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11118[3]0.0261982–0.366469 1/AHas uncertainty columnMissing 00sasbdb/entries/a5/sasdga5/source/SASDGA5.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)7.5—Å
i0Guinier17.60.05arbitrary
i0P(r)17.45—arbitrary
mwExperimental26.0—kDa
mwPorod29.0—kDa
porod_volumePorod48.6—ų
rgGuinier2.230.1Å
rgP(r)2.23—Å

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

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3. Source Fits and Models Source Fits & Models

Fit 1 · MultiFoXS

χ²: 1.5473CorMap p: 0.000262Unit: 1/A
ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—atomicMultiFoXS —23.59—Model Image

Fit 3 · DAMMIN

χ²: 1.456CorMap p: 0.998201Unit: 1/A
ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—dummyDAMFILT DAMFILT 5.0 (r4547)—26.604—Model Image
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4. Source File Index Source Files

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5. Experiment Description and Publication Experiment & Publication

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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 name25 mM HEPES 400 mM LiCl 10% v/v glycerolBuffer concentration—
pH7.5Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2016-03-16Storage / measurement temperature— / 25.0
Exposure time—Frames—
Wavelength0.103Sample-to-detector distance3.5
SourceX-ray synchrotronDetectorPilatus3 X 1M
Facility / beamlineAdvanced Photon Source (APS), Argonne National Laboratory / BioCAT 18ID · Lemont, IL, USA
q range0.262 – 3.665Sample volume / flow rate500.0 / 0.6

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:202 field values
Field pathRaw value
codeSASDGA5
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleStructural basis of cell surface signaling by a conserved sigma regulator in Gram-negative bacteria.
project.publication.titleStructural basis of cell surface signaling by a conserved sigma regulator in Gram-negative bacteria.
project.publication.author_listJensen JL, Jernberg BD, Sinha S, Colbert CL
project.publication.journalJ Biol Chem
project.publication.doi10.1074/jbc.RA119.010697
project.publication.pmid32107313
project.publication.published_date2020 Feb 26
project.statusreleased
project.submitted_date2019-09-16
project.released_date2020-03-03
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experiment.instrument.detector.namePilatus3 X 1M
experiment.instrument.detector.resolution0.172
experiment.instrument.nameAdvanced Photon Source (APS), Argonne National Laboratory
experiment.instrument.cityLemont, IL
experiment.instrument.countryUSA
experiment.instrument.beamline_nameBioCAT 18ID
experiment.instrument.beam_geometrynull
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_namePupR protein
experiment.sample.molecule[0].short_namePupR
experiment.sample.molecule[0].sequenceGAMGQDWRADYHSRIGEQRRLTLADGTQVQLNTDSALNVA FDQQARRLRLVRGEMLITRPALADSRPLWVDTEHGRLESTL AQFNVRLHGQHTQATVYQGSVALQPALHAYPPILLGAGEQA SFNQQGLLARQAVAAVAPAWSQGMLVAQGQPLAAFIEDLAR YRRGHLACDPALAGLRVSGTFPLENTDKIIAAVAETLQLEVQ HFTRYWVTLKPRMA
experiment.sample.molecule[0].organismPseudomonas putida
experiment.sample.molecule[0].uniprot_codeQ52209
experiment.sample.molecule[0].uniprot_range_first110
experiment.sample.molecule[0].uniprot_range_last324
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMNGQGATSIPGEVAEQAMHWHLELQEPAVSAATLAACMSWRQAHPLHEHAWQRTQVFAQR LREMRSPGQRPLAHAALRPQQSRRTALKQLSLLMAAGAGAWYLKDAALVQDWRADYHSRI GEQRRLTLADGTQVQLNTDSALNVAFDQQARRLRLVRGEMLITRPALADSRPLWVDTEHG RLESTLAQFNVRLHGQHTQATVYQGSVALQPALHAYPPILLGAGEQASFNQQGLLARQAV AAVAPAWSQGMLVAQGQPLAAFIEDLARYRRGHLACDPALAGLRVSGTFPLENTDKIIAA VAETLQLEVQHFTRYWVTLKPRMA
experiment.sample.molecule[0].mw24.124
experiment.sample.molecule[0].total_mw24.124
experiment.sample.molecule[0].number_molecules1
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.name25 mM HEPES 400 mM LiCl 10% 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.ph7.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameThe C-terminal cell-surface signaling domain of the Pseudomonas capeferrum anti-sigma regulator PupR
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_namenull
experiment.contributor[0].affiliation[0].addressnull
experiment.contributor[0].affiliation[0].full_nameVanderbilt University
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameJaime
experiment.contributor[0].contributor_surnameJensen
experiment.contributor[0].orcidhttps://orcid.org/0000-0002-8818-7513
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2016-03-16
experiment.storage_temperaturenull
experiment.cell_temperature25.0
experiment.exposure_timenull
experiment.number_of_framesnull
experiment.wavelength0.103
experiment.sample_detector_distance3.5
experiment.concentration_minnull
experiment.concentration_max9.6
experiment.sample_volume500.0
experiment.flow_rate0.6
experiment.s_min0.262
experiment.s_max3.665
experiment.total_exposure_timenull
experiment.seccolumn1
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pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of the C-terminal cell-surface signaling domain of PupR in 25 mM HEPES 400 mM LiCl 10% v/v glycerol, pH 7.5 were collected on the BioCAT 18ID beam line at the Advanced Photon Source (APS), Argonne National Laboratory (Lemont, IL, USA) using a Pilatus3 X 1M detector at a sample-detector distance of 3.5 m and at a wavelength of λ = 0.103 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 500.00 μl sample at 9.6 mg/ml was injected at a 0.60 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 25°C. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of an appropriate solvent-blank was subtracted from the SEC elution peak of the sample.
tags[]
intensity_unitarbitrary
experimental_mw26.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw29.0
porod_mw_errornull
pddf_i017.45
pddf_i0_errornull
guinier_i017.6
guinier_i0_error0.05
pddf_rg2.23
pddf_rg_errornull
guinier_rg2.23
guinier_rg_error0.1
pddf_dmax7.5
pddf_dmax_errornull
porod_volume48.6
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last106
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDGA5_datloglog_img.png
symmetrynull
last_modified2020-03-03T14:59:07.808703+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDGA5
statussuccess
started_at2026-08-11T14:43:12.828780+00:00
finished_at2026-08-11T14:43:26.930824+00:00
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View the complete summary.json source
{
  "code": "SASDGA5",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "Structural basis of cell surface signaling by a conserved sigma regulator in Gram-negative bacteria.",
    "publication": {
      "title": "Structural basis of cell surface signaling by a conserved sigma regulator in Gram-negative bacteria.",
      "author_list": "Jensen JL, Jernberg BD, Sinha S, Colbert CL",
      "journal": "J Biol Chem",
      "doi": "10.1074/jbc.RA119.010697",
      "pmid": "32107313",
      "published_date": "2020 Feb 26"
    },
    "status": "released",
    "submitted_date": "2019-09-16",
    "released_date": "2020-03-03"
  },
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  "experiment": {
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View the complete manifest.json source
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