SASDG46

4-hydroxy-tetrahydrodipicolinate synthase (N84A mutant)

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2021-04-22T13:41:34.336316+02:00

The models displayed in this entry represent: Top, the averaged (DAMFILT) model obtained from the spatial alignment of several individual DAMMIF models (volume and bead occupancy corrected) and; Bottom, and individual DAMMIF model representative and corresponding fit. Additional individual DAMMIF models (in P1 symmetry) are provided in the full entry zip archive.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · 4-hydroxy-tetrahydrodipicolinate synthase (N84A mutant)

Concentration— – 10.0 Buffer / pH20 mM Tris-HCl, 150 mM NaCl / 8.0
Experimental temperature— Facility / beamlineDiamond Light Source / B21
Wavelength0.1 nmExposure3.0 s × 619

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
4-hydroxy-tetrahydrodipicolinate synthase (N84A mutant)
View sequence
MDKNIIIGAMTALITPFKNGKVDEQSYARLIKRQIENGIDAVVPVGTTGESATLTHEEHRTCIEIAVETCKGTKVKVLAGAGSAATHEAVGLAKFAKEHGADGILSVAPYYNKPTQQGLYEHYKAIAQSVDIPVLLYNVPGRTGCEISTDTIIKLFRDCENIYGVKEASGNIDKCVDLLAHEPRMMLISGEDAINYPILSNGGKGVISVTSNLLPDMISALTHFALDENYKEAKKINDELYNINKILFCESNPIPIKTAMYLAGLIESLEFRLPLCSPSKENFAKIEEVMKKYKIKGF
proteinCampylobacter jejuniQ9PPB41–298unknownMolecule count —32.627 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11702[3]0.0039–0.38954656 1/AHas uncertainty columnMissing 04sasbdb/entries/46/sasdg46/source/SASDG46.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)8.9—Å
i0Guinier0.1636999e-05arbitrary
i0P(r)0.16124e-05arbitrary
mwExperimental109.0—kDa
mwPorod101.0—kDa
porod_volumePorod163.0—ų
rgGuinier3.330.03Å
rgP(r)3.240.06Å

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

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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 name20 mM Tris-HCl, 150 mM NaClBuffer concentration—
pH8.0Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2017-08-02Storage / measurement temperature— / —
Exposure time3.0Frames619
Wavelength0.1Sample-to-detector distance4.0
SourceX-ray synchrotronDetectorPilatus 2M
Facility / beamlineDiamond Light Source / B21 · Didcot, UK
q range0.039 – 3.895Sample volume / flow rate50.0 / 0.16

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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pddf:source record
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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:169 field values
Field pathRaw value
codeSASDG46
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleAsparagine-84, a regulatory allosteric site residue, helps maintain the quaternary structure of Campylobacter jejuni dihydrodipicolinate synthase.
project.publication.titleAsparagine-84, a regulatory allosteric site residue, helps maintain the quaternary structure of Campylobacter jejuni dihydrodipicolinate synthase.
project.publication.author_listMajdi Yazdi M, Saran S, Mrozowich T, Lehnert C, Patel TR, Sanders DAR, Palmer DRJ
project.publication.journalJ Struct Biol
project.publication.doi10.1016/j.jsb.2019.107409
project.publication.pmid31678256
project.publication.published_date2019 Oct 31
project.statusreleased
project.submitted_date2019-09-29
project.released_date2019-11-17
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experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus 2M
experiment.instrument.detector.resolutionnull
experiment.instrument.nameDiamond Light Source
experiment.instrument.cityDidcot
experiment.instrument.countryUK
experiment.instrument.beamline_nameB21
experiment.instrument.beam_geometry1 x 5 mm
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_name4-hydroxy-tetrahydrodipicolinate synthase (N84A mutant)
experiment.sample.molecule[0].short_nameHTPA synthase N84A
experiment.sample.molecule[0].sequenceMDKNIIIGAMTALITPFKNGKVDEQSYARLIKRQIENGIDAVVPVGTTGESATLTHEEHRTCIEIAVETCKGTKVKVLAGAGSAATHEAVGLAKFAKEHGADGILSVAPYYNKPTQQGLYEHYKAIAQSVDIPVLLYNVPGRTGCEISTDTIIKLFRDCENIYGVKEASGNIDKCVDLLAHEPRMMLISGEDAINYPILSNGGKGVISVTSNLLPDMISALTHFALDENYKEAKKINDELYNINKILFCESNPIPIKTAMYLAGLIESLEFRLPLCSPSKENFAKIEEVMKKYKIKGF
experiment.sample.molecule[0].organismCampylobacter jejuni
experiment.sample.molecule[0].uniprot_codeQ9PPB4
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last298
experiment.sample.molecule[0].oligomerizationunknown
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMDKNIIIGAMTALITPFKNGKVDEQSYARLIKRQIENGIDAVVPVGTTGESATLTHEEHR TCIEIAVETCKGTKVKVLAGAGSNATHEAVGLAKFAKEHGADGILSVAPYYNKPTQQGLY EHYKAIAQSVDIPVLLYNVPGRTGCEISTDTIIKLFRDCENIYGVKEASGNIDKCVDLLA HEPRMMLISGEDAINYPILSNGGKGVISVTSNLLPDMISALTHFALDENYKEAKKINDEL YNINKILFCESNPIPIKTAMYLAGLIESLEFRLPLCSPSKENFAKIEEVMKKYKIKGF
experiment.sample.molecule[0].mw32.627
experiment.sample.molecule[0].total_mw32.627
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.name20 mM Tris-HCl, 150 mM NaCl
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph8.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.name4-hydroxy-tetrahydrodipicolinate synthase (N84A mutant)
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].addressLethbridge, AB, Canada
experiment.contributor[0].affiliation[0].full_nameUniversity of Lethbridge
experiment.contributor[0].affiliation[0].webpagehttp://www.uleth.ca/
experiment.contributor[0].contributor_nameTrushar
experiment.contributor[0].contributor_surnamePatel
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2017-08-02
experiment.storage_temperaturenull
experiment.cell_temperaturenull
experiment.exposure_time3.0
experiment.number_of_frames619
experiment.wavelength0.1
experiment.sample_detector_distance4.0
experiment.concentration_minnull
experiment.concentration_max10.0
experiment.sample_volume50.0
experiment.flow_rate0.16
experiment.s_min0.039
experiment.s_max3.895
experiment.total_exposure_timenull
experiment.seccolumn1
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fits[0].p_value0.0
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fits[0].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionThe models displayed in this entry represent: Top, the averaged (DAMFILT) model obtained from the spatial alignment of several individual DAMMIF models (volume and bead occupancy corrected) and; Bottom, and individual DAMMIF model representative and corresponding fit. Additional individual DAMMIF models (in P1 symmetry) are provided in the full entry zip archive.
experiment_descriptionSynchrotron SAXS data from solutions of N84A mutant 4-hydroxy-tetrahydrodipicolinate synthase in 20 mM Tris-HCl, 150 mM NaCl, pH 8 were collected on the B21 beam line at the Diamond Light Source (Didcot, UK) using a Pilatus 2M detector at a sample-detector distance of 4 m and at a wavelength of λ = 0.1 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 50.00 μl sample at 10 mg/ml was injected at a 0.16 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column . 619 successive 3 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[]
intensity_unitarbitrary
experimental_mw109.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw101.0
porod_mw_errornull
pddf_i00.1612
pddf_i0_error4e-05
guinier_i00.163699
guinier_i0_error9e-05
pddf_rg3.24
pddf_rg_error0.06
guinier_rg3.33
guinier_rg_error0.03
pddf_dmax8.9
pddf_dmax_errornull
porod_volume163.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first65
guinier_point_last155
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDG46_datloglog_img.png
symmetrynull
last_modified2021-04-22T13:41:34.336316+02:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDG46
statussuccess
started_at2026-08-11T15:01:24.534188+00:00
finished_at2026-08-11T15:01:34.954186+00:00
source_last_modified2021-04-22T13:41:34.336316+02:00
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View the complete summary.json source
{
  "code": "SASDG46",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "Asparagine-84, a regulatory allosteric site residue, helps maintain the quaternary structure of Campylobacter jejuni dihydrodipicolinate synthase.",
    "publication": {
      "title": "Asparagine-84, a regulatory allosteric site residue, helps maintain the quaternary structure of Campylobacter jejuni dihydrodipicolinate synthase.",
      "author_list": "Majdi Yazdi M, Saran S, Mrozowich T, Lehnert C, Patel TR, Sanders DAR, Palmer DRJ",
      "journal": "J Struct Biol",
      "doi": "10.1016/j.jsb.2019.107409",
      "pmid": "31678256",
      "published_date": "2019 Oct 31"
    },
    "status": "released",
    "submitted_date": "2019-09-29",
    "released_date": "2019-11-17"
  },
  "pddf_data": "https://www.sasbdb.org/media/p_of_R_files/SASDG46.out",
  "intensities_data": "https://www.sasbdb.org/media/intensities_files/SASDG46.dat",
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      },
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      "city": "Didcot",
      "country": "UK",
      "beamline_name": "B21",
      "beam_geometry": "1 x 5 mm",
      "type_of_source": "X-ray synchrotron",
      "point_source": null,
      "line_collimation": null,
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    "sample": {
      "molecule": [
        {
          "long_name": "4-hydroxy-tetrahydrodipicolinate synthase (N84A mutant)",
          "short_name": "HTPA synthase N84A",
          "sequence": "MDKNIIIGAMTALITPFKNGKVDEQSYARLIKRQIENGIDAVVPVGTTGESATLTHEEHRTCIEIAVETCKGTKVKVLAGAGSAATHEAVGLAKFAKEHGADGILSVAPYYNKPTQQGLYEHYKAIAQSVDIPVLLYNVPGRTGCEISTDTIIKLFRDCENIYGVKEASGNIDKCVDLLAHEPRMMLISGEDAINYPILSNGGKGVISVTSNLLPDMISALTHFALDENYKEAKKINDELYNINKILFCESNPIPIKTAMYLAGLIESLEFRLPLCSPSKENFAKIEEVMKKYKIKGF",
          "organism": "Campylobacter jejuni",
          "uniprot_code": "Q9PPB4",
          "uniprot_range_first": 1,
          "uniprot_range_last": 298,
          "oligomerization": "unknown",
          "molecular_type": "protein",
          "uniprot_sequence": "MDKNIIIGAMTALITPFKNGKVDEQSYARLIKRQIENGIDAVVPVGTTGESATLTHEEHR\nTCIEIAVETCKGTKVKVLAGAGSNATHEAVGLAKFAKEHGADGILSVAPYYNKPTQQGLY\nEHYKAIAQSVDIPVLLYNVPGRTGCEISTDTIIKLFRDCENIYGVKEASGNIDKCVDLLA\nHEPRMMLISGEDAINYPILSNGGKGVISVTSNLLPDMISALTHFALDENYKEAKKINDEL\nYNINKILFCESNPIPIKTAMYLAGLIESLEFRLPLCSPSKENFAKIEEVMKKYKIKGF",
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          "deuteration": null,
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          "molecule_description": null
        }
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        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
        "pka": null,
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      },
      "purity_method": null,
      "name": "4-hydroxy-tetrahydrodipicolinate synthase (N84A mutant)",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
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    "contributor": [
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        "affiliation": [
          {
            "short_name": null,
            "address": "Lethbridge, AB, Canada",
            "full_name": "University of Lethbridge",
            "webpage": "http://www.uleth.ca/"
          }
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        "contributor_name": "Trushar",
        "contributor_surname": "Patel",
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    "concentration_method": null,
    "concentration_unit": null,
    "date": "2017-08-02",
    "storage_temperature": null,
    "cell_temperature": null,
    "exposure_time": 3.0,
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    "wavelength": 0.1,
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    "total_exposure_time": null,
    "seccolumn": 1
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  "intensities_log_log_plot": "SASDG46_datloglog_img.png",
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  "last_modified": "2021-04-22T13:41:34.336316+02:00",
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}
View the complete manifest.json source
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