SASDFX2

Cell wall synthesis protein Wag31(T73A) polymer (SEC-frames 305-309)

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2020-08-13T15:34:35.760459+02:00

SEC-SAXS was performed at room temperature using the following parameters: Column: Superdex 200 PC3.2; Flow rate: 0.05 mL/min; Sample injection concentration: 2.4 mg/mL; Injection volume: 100 μL. 500 successive 1 second frames were collected through the SEC-elution peak. SEC-SAXS data of Cell wall synthesis protein Wag31(T73A) polymer frame no. 305-309

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Cell wall synthesis protein Wag31(T73A) polymer (SEC-frames 305-309)

Concentration— – 2.4 Buffer / pH50mM Tris pH7.5, 300mM NaCl, 10% Glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME) / 7.5
Experimental temperature23.0 Facility / beamlineStanford Synchrotron Radiation Lightsource (SSRL) / BL4-2
Wavelength0.1 nmExposure1.0 s × 500

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Cell wall synthesis protein Wag31
View sequence
MHHHHHHENLYFQGPLTPADVHNVAFSKPPIGKRGYNEDEVDAFLDLVENELTRLIEENSDLRQRINELDQELAAGGGAGVTPQAEQAIPAYEPEPGKPAPAAVSAGMNEEQALKAARVLSLAQDTADRLTNTAKAESDKMLADARANAEQILGEARHTADATVAEARQRADAMLADAQSRSEAQLRQAQEKADALQADAERKHSEIMGTINQQRAVLEGRLEQLRTFEREYRTRLKTYLESQLEELGQRGSAAPVDSNADAGGFDQFNRGKN
proteinMycobacterium tuberculosisP9WMU1—–—unknownMolecule count —29.98 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
1946[3]0.00554855–0.402288 1/AHas uncertainty columnMissing 0311sasbdb/entries/x2/sasdfx2/source/SASDFX2.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
i0Guinier24.69—arbitrary
mwExperimental29.92—kDa
rgGuinier11.05—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

This entry has no source fit record.

▶

4. Source File Index Source Files

▶

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 name50mM Tris pH7.5, 300mM NaCl, 10% Glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME)Buffer concentration—
pH7.5Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2018-01-29Storage / measurement temperature23.0 / 23.0
Exposure time1.0Frames500
Wavelength0.1Sample-to-detector distance2.54
SourceX-ray synchrotronDetectorRayonix MX225-HE
Facility / beamlineStanford Synchrotron Radiation Lightsource (SSRL) / BL4-2 · Menlo Park, CA, USA
q range0.055 – 4.023Sample 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

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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:134 field values
Field pathRaw value
codeSASDFX2
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleHigher order assembling of the mycobacterial polar growth factor DivIVA/Wag31.
project.publication.titleHigher order assembling of the mycobacterial polar growth factor DivIVA/Wag31.
project.publication.author_listChoukate K, Gupta A, Basu B, Virk K, Ganguli M, Chaudhuri B
project.publication.journalJ Struct Biol
project.publication.doi10.1016/j.jsb.2019.107429
project.publication.pmid31778770
project.publication.published_date2019 Nov 25
project.statusreleased
project.submitted_date2019-01-30
project.released_date2020-01-09
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experiment.instrument.detector.resolutionnull
experiment.instrument.nameStanford Synchrotron Radiation Lightsource (SSRL)
experiment.instrument.cityMenlo Park, CA
experiment.instrument.countryUSA
experiment.instrument.beamline_nameBL4-2
experiment.instrument.beam_geometrynull
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
experiment.instrument.line_collimationnull
experiment.instrument.sample_path_lengthnull
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experiment.sample.molecule[0].long_nameCell wall synthesis protein Wag31
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceMHHHHHHENLYFQGPLTPADVHNVAFSKPPIGKRGYNEDEVDAFLDLVENELTRLIEENSDLRQRINELDQEL AAGGGAGVTPQAEQAIPAYEPEPGKPAPAAVSAGMNEEQALKAARVLSLAQDTADRLTNT AKAESDKMLADARANAEQILGEARHTADATVAEARQRADAMLADAQSRSEAQLRQAQEKA DALQADAERKHSEIMGTINQQRAVLEGRLEQLRTFEREYRTRLKTYLESQLEELGQRGSA APVDSNADAGGFDQFNRGKN
experiment.sample.molecule[0].organismMycobacterium tuberculosis
experiment.sample.molecule[0].uniprot_codeP9WMU1
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationunknown
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMPLTPADVHNVAFSKPPIGKRGYNEDEVDAFLDLVENELTRLIEENSDLRQRINELDQEL AAGGGAGVTPQATQAIPAYEPEPGKPAPAAVSAGMNEEQALKAARVLSLAQDTADRLTNT AKAESDKMLADARANAEQILGEARHTADATVAEARQRADAMLADAQSRSEAQLRQAQEKA DALQADAERKHSEIMGTINQQRAVLEGRLEQLRTFEREYRTRLKTYLESQLEELGQRGSA APVDSNADAGGFDQFNRGKN
experiment.sample.molecule[0].mw29.98
experiment.sample.molecule[0].total_mw29.98
experiment.sample.molecule[0].number_molecules0
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.name50mM Tris pH7.5, 300mM NaCl, 10% Glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME)
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.nameCell wall synthesis protein Wag31(T73A) polymer (SEC-frames 305-309)
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_nameCSIR
experiment.contributor[0].affiliation[0].addressChandigarh, India
experiment.contributor[0].affiliation[0].full_nameCSIR-Institute of Microbial Technology
experiment.contributor[0].affiliation[0].webpagehttp://www.imtech.res.in/
experiment.contributor[0].contributor_nameKomal
experiment.contributor[0].contributor_surnameChoukate
experiment.contributor[0].orcid
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2018-01-29
experiment.storage_temperature23.0
experiment.cell_temperature23.0
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estimated_volume_methodnull
pddf_softwarenull
pddf_software_versionnull
i0_calibration_standardnull
descriptionSEC-SAXS was performed at room temperature using the following parameters: Column: Superdex 200 PC3.2; Flow rate: 0.05 mL/min; Sample injection concentration: 2.4 mg/mL; Injection volume: 100 μL. 500 successive 1 second frames were collected through the SEC-elution peak. SEC-SAXS data of Cell wall synthesis protein Wag31(T73A) polymer frame no. 305-309
experiment_descriptionSynchrotron SAXS data from solutions of Cell wall synthesis protein Wag31(T73A) polymer (SEC-frames 305-309) in 50mM Tris pH7.5, 300mM NaCl, 10% Glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME), pH 7.5 were collected on the BL4-2 beam line at the Stanford Synchrotron Radiation Lightsource (SSRL) storage ring (Stanford, CA, USA) using a Rayonix MX225-HE detector at a sample-detector distance of 2.5 m and at a wavelength of λ = 0.1 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 2.40 mg/ml was measured at 23°C. 500 successive 1 second 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.
tags[]
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i0_calibration_standard_datanull
intensities_log_log_plotSASDFX2_datloglog_img.png
symmetrynull
last_modified2020-08-13T15:34:35.760459+02:00
bragg_peak[]
manifest.json:33 field values
Field pathRaw value
codeSASDFX2
statussuccess
started_at2026-08-11T13:48:26.468210+00:00
finished_at2026-08-11T13:48:33.955726+00:00
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View the complete summary.json source
{
  "code": "SASDFX2",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "Higher order assembling of the mycobacterial polar growth factor DivIVA/Wag31.",
    "publication": {
      "title": "Higher order assembling of the mycobacterial polar growth factor DivIVA/Wag31.",
      "author_list": "Choukate K, Gupta A, Basu B, Virk K, Ganguli M, Chaudhuri B",
      "journal": "J Struct Biol",
      "doi": "10.1016/j.jsb.2019.107429",
      "pmid": "31778770",
      "published_date": "2019 Nov 25"
    },
    "status": "released",
    "submitted_date": "2019-01-30",
    "released_date": "2020-01-09"
  },
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          "long_name": "Cell wall synthesis protein Wag31",
          "short_name": null,
          "sequence": "MHHHHHHENLYFQGPLTPADVHNVAFSKPPIGKRGYNEDEVDAFLDLVENELTRLIEENSDLRQRINELDQEL\r\nAAGGGAGVTPQAEQAIPAYEPEPGKPAPAAVSAGMNEEQALKAARVLSLAQDTADRLTNT\r\nAKAESDKMLADARANAEQILGEARHTADATVAEARQRADAMLADAQSRSEAQLRQAQEKA\r\nDALQADAERKHSEIMGTINQQRAVLEGRLEQLRTFEREYRTRLKTYLESQLEELGQRGSA\r\nAPVDSNADAGGFDQFNRGKN",
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View the complete manifest.json source
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