SASDAC8

SDS hydrolase SdsA1

Data type: SASBDB experimental data Status: Published Curve type: Single concentration Last updated: 2019-12-06T13:07:15.624532+01:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · SDS hydrolase SdsA1

Concentration— – 12.2 mg/mlBuffer / pH50 mM HEPES / 7.0
Experimental temperature— Facility / beamlineNational Synchrotron Light Source (NSLS) / X9A
Wavelength0.091 nmExposure30.0 s × 6

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Pseudomonas aeruginosa SDS hydrolase SdsA1
View sequence
MSRLLALLALAPLLAGAAETTAPKPPSAFTVEAQRRVEAELPFADRADFERADRGLIRRPERLLIRNPDGSVAWQLGGYDFLLDGKPRDSINPSLQRQALLNLKYGLFEVAEGIYQVRGFDLANITFIRGDSGWIVVDTLTTPATARAAYELVSRELGERPIRTVIYSHAHADHFGGVRGLVEPQQVASGAVQIIAPAGFMEAAIKENVLAGNAMMRRATYQYGTQLPKGPQGQVDMAIGKGLARGPLSLLAPTRLIEGEGEDLVLDGVPFTFQNTPGTESPAEMNIWLPRQKALLMAENVVGTLHNLYTLRGAEVRDALGWSKYINQALHRFGRQAEVMFAVHNWPRWGNAEIVEVLEKQRDLYGYLHDQTLHLANQGVTIGQVHNRLRLPPSLDQEWYDRGYHGSVSHNARAVLNRYLGYYDGNPATLDPLSPEDSAGRYVEYMGGAERLLEQARASYARGEYRWVVEVVNRLVFAEPDNRAARELQADALEQLGYQAENAGWRNSYLSAAYELRHGVPRDQPTMKAGSADALAAMDTGLLFDYLGVRLDAGAAEGKALSINLRLPDIGENYLLELKNSHLNNLRGVQSEDAGQTVSIDRADLNRLLLKEVSAVRLVFEGKLKSSGNPLLLGQLFGMLGDFDFWFDIVTPAAKSEG
proteinPseudomonas aeruginosaQ9I5I9—–—dimerMolecule count 272.591 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
1219[3]0.08–19.6 1/nmHas uncertainty columnMissing 00sasbdb/entries/c8/sasdac8/source/SASDAC8.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)16.9—nm
i0Guinier1590.0——
i0P(r)1607.0——
mwExperimental140.0—kDa
mwPorod153.0—kDa
porod_volumePorod261.0—nm³
rgGuinier3.60.89nm
rgP(r)3.66—nm

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 name50 mM HEPESBuffer concentration50.0 mM
pH7.0Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2013-07-22Storage / measurement temperature20.0 / —
Exposure time30.0Frames6
Wavelength0.091Sample-to-detector distance3.4
SourceX-ray synchrotronDetectorPilatus 300K
Facility / beamlineNational Synchrotron Light Source (NSLS) / X9A · Brookhaven, NY, USA
q range0.08 – 19.6Sample 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:157 field values
Field pathRaw value
codeSASDAC8
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleSdsA polymorph isolation and improvement of their crystal quality using nonconventional crystallization techniques
project.publication.titleSdsA polymorph isolation and improvement of their crystal quality using nonconventional crystallization techniques
project.publication.author_listDe la Mora E, Flores-Hernández E, Jakoncic J, Stojanoff V, Siliqi D, Sánchez-Puig N, Moreno A
project.publication.journalJournal of Applied Crystallography
project.publication.doi10.1107/S1600576715016556
project.publication.pmidnull
project.publication.published_date2015 Oct 1
project.statusreleased
project.submitted_date2015-05-17
project.released_date2015-09-20
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDAC8.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDAC8.dat
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pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDAC8_pofr_img.png
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experiment.instrument.detector.type20Hz
experiment.instrument.detector.namePilatus 300K
experiment.instrument.detector.resolutionnull
experiment.instrument.nameNational Synchrotron Light Source (NSLS)
experiment.instrument.cityBrookhaven, NY
experiment.instrument.countryUSA
experiment.instrument.beamline_nameX9A
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_namePseudomonas aeruginosa SDS hydrolase SdsA1
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceMSRLLALLALAPLLAGAAETTAPKPPSAFTVEAQRRVEAELPFADRADFERADRGLIRRPERLLIRNPDGSVAWQLGGYDFLLDGKPRDSINPSLQRQALLNLKYGLFEVAEGIYQVRGFDLANITFIRGDSGWIVVDTLTTPATARAAYELVSRELGERPIRTVIYSHAHADHFGGVRGLVEPQQVASGAVQIIAPAGFMEAAIKENVLAGNAMMRRATYQYGTQLPKGPQGQVDMAIGKGLARGPLSLLAPTRLIEGEGEDLVLDGVPFTFQNTPGTESPAEMNIWLPRQKALLMAENVVGTLHNLYTLRGAEVRDALGWSKYINQALHRFGRQAEVMFAVHNWPRWGNAEIVEVLEKQRDLYGYLHDQTLHLANQGVTIGQVHNRLRLPPSLDQEWYDRGYHGSVSHNARAVLNRYLGYYDGNPATLDPLSPEDSAGRYVEYMGGAERLLEQARASYARGEYRWVVEVVNRLVFAEPDNRAARELQADALEQLGYQAENAGWRNSYLSAAYELRHGVPRDQPTMKAGSADALAAMDTGLLFDYLGVRLDAGAAEGKALSINLRLPDIGENYLLELKNSHLNNLRGVQSEDAGQTVSIDRADLNRLLLKEVSAVRLVFEGKLKSSGNPLLLGQLFGMLGDFDFWFDIVTPAAKSEG
experiment.sample.molecule[0].organismPseudomonas aeruginosa
experiment.sample.molecule[0].uniprot_codeQ9I5I9
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMSRLLALLALAPLLAGAAETTAPKPPSAFTVEAQRRVEAELPFADRADFERADRGLIRRP ERLLIRNPDGSVAWQLGGYDFLLDGKPRDSINPSLQRQALLNLKYGLFEVAEGIYQVRGF DLANITFIRGDSGWIVVDTLTTPATARAAYELVSRELGERPIRTVIYSHAHADHFGGVRG LVEPQQVASGAVQIIAPAGFMEAAIKENVLAGNAMMRRATYQYGTQLPKGPQGQVDMAIG KGLARGPLSLLAPTRLIEGEGEDLVLDGVPFTFQNTPGTESPAEMNIWLPRQKALLMAEN VVGTLHNLYTLRGAEVRDALGWSKYINQALHRFGRQAEVMFAVHNWPRWGNAEIVEVLEK QRDLYGYLHDQTLHLANQGVTIGQVHNRLRLPPSLDQEWYDRGYHGSVSHNARAVLNRYL GYYDGNPATLDPLSPEDSAGRYVEYMGGAERLLEQARASYARGEYRWVVEVVNRLVFAEP DNRAARELQADALEQLGYQAENAGWRNSYLSAAYELRHGVPRDQPTMKAGSADALAAMDT GLLFDYLGVRLDAGAAEGKALSINLRLPDIGENYLLELKNSHLNNLRGVQSEDAGQTVSI DRADLNRLLLKEVSAVRLVFEGKLKSSGNPLLLGQLFGMLGDFDFWFDIVTPAAKSEG
experiment.sample.molecule[0].mw72.591
experiment.sample.molecule[0].total_mw145.183
experiment.sample.molecule[0].number_molecules2
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 HEPES
experiment.sample.buffer.concentration_unitmM
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentration50.0
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameSDS hydrolase SdsA1
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[]
experiment.contributor[0].contributor_nameEugenio
experiment.contributor[0].contributor_surnameDe la Mora
experiment.contributor[0].orcidnull
experiment.contributor[1].affiliation[]
experiment.contributor[1].contributor_nameDritan
experiment.contributor[1].contributor_surnameSiliqi
experiment.contributor[1].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitmg/ml
experiment.date2013-07-22
experiment.storage_temperature20.0
experiment.cell_temperaturenull
experiment.exposure_time30.0
experiment.number_of_frames6
experiment.wavelength0.091
experiment.sample_detector_distance3.4
experiment.concentration_minnull
experiment.concentration_max12.2
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.08
experiment.s_max19.6
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].models[0].softwareCRYSOL
fits[0].models[0].pdb_link[]
fits[0].models[0].model_titlenull
fits[0].models[0].type_of_modelatomic
fits[0].models[0].software_version
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fits[0].models[0].model_mw139.5
fits[0].models[0].bead_radius1.9
fits[0].models[0].lognull
fits[0].models[0].symmetry
fits[0].models[0].comment
fits[0].models[0].user67
fits[0].fit_unit1/A
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fits[0].softwarenull
fits[0].chi_square_value7.14
fits[0].p_value0.0
fits[0].fit_residual_plotSASDAC8_fit1_fitresiduals_img.png
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fits[0].fit_lognull
fits[0].software_versionnull
fits[0].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versiongnom
i0_calibration_standardnull
descriptionnull
experiment_descriptionX-ray synchrotron radiation scattering data from solutions of Pseudomonas aeruginosa SDS hydrolase SdsA1 in 50 mM HEPES were collected on the X9A camera on the storage ring NSLS (Brookhaven, USA). Using a 20Hz Pilatus 300K detector as SAXS detector (located at 3.4m from the sample) and a custom-designed Photonic Science CCD detector as WAXS detector (located at 20cm from the sample). Together, these two detectors cover a combined s range of 0.08 -19.600 nm-1, with overlapping data between 1.2 and 2.0 nm-1 (s = 4π sin θ/λ, where 2θ is the scattering angle). One solute concentration of 12.20 mg/ml was measured. Six successive 30 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 and the different curves were scaled for protein concentration. The low angle data collected were obtained from a single concentration scattering curve. For SAXS data analysis (RG, Pr function) we used the data up to 2.0 nm-1.
tags[0]waxs
intensity_unitnull
experimental_mw140.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw153.0
porod_mw_errornull
pddf_i01607.0
pddf_i0_errornull
guinier_i01590.0
guinier_i0_errornull
pddf_rg3.66
pddf_rg_errornull
guinier_rg3.6
guinier_rg_error0.89
pddf_dmax16.9
pddf_dmax_errornull
porod_volume261.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_firstnull
guinier_point_lastnull
pddf_point_first11
pddf_point_last100
i0_calibration_standard_datanull
intensities_log_log_plotSASDAC8_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDAC8
statussuccess
started_at2026-08-11T15:50:10.051453+00:00
finished_at2026-08-11T15:50:24.080806+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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View the complete summary.json source
{
  "code": "SASDAC8",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
  "project": {
    "title": "SdsA polymorph isolation and improvement of their crystal quality using nonconventional crystallization techniques",
    "publication": {
      "title": "SdsA polymorph isolation and improvement of their crystal quality using nonconventional crystallization techniques",
      "author_list": "De la Mora E, Flores-Hernández E, Jakoncic J, Stojanoff V, Siliqi D, Sánchez-Puig N, Moreno A",
      "journal": "Journal of Applied Crystallography",
      "doi": "10.1107/S1600576715016556 ",
      "pmid": null,
      "published_date": "2015 Oct 1"
    },
    "status": "released",
    "submitted_date": "2015-05-17",
    "released_date": "2015-09-20"
  },
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  "pddf_plot": "https://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDAC8_pofr_img.png",
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  "experiment": {
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        "name": "Pilatus 300K",
        "resolution": null
      },
      "name": "National Synchrotron Light Source (NSLS)",
      "city": "Brookhaven, NY",
      "country": "USA",
      "beamline_name": "X9A",
      "beam_geometry": "",
      "type_of_source": "X-ray synchrotron",
      "point_source": null,
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    },
    "sample": {
      "molecule": [
        {
          "long_name": "Pseudomonas aeruginosa SDS hydrolase SdsA1",
          "short_name": null,
          "sequence": "MSRLLALLALAPLLAGAAETTAPKPPSAFTVEAQRRVEAELPFADRADFERADRGLIRRPERLLIRNPDGSVAWQLGGYDFLLDGKPRDSINPSLQRQALLNLKYGLFEVAEGIYQVRGFDLANITFIRGDSGWIVVDTLTTPATARAAYELVSRELGERPIRTVIYSHAHADHFGGVRGLVEPQQVASGAVQIIAPAGFMEAAIKENVLAGNAMMRRATYQYGTQLPKGPQGQVDMAIGKGLARGPLSLLAPTRLIEGEGEDLVLDGVPFTFQNTPGTESPAEMNIWLPRQKALLMAENVVGTLHNLYTLRGAEVRDALGWSKYINQALHRFGRQAEVMFAVHNWPRWGNAEIVEVLEKQRDLYGYLHDQTLHLANQGVTIGQVHNRLRLPPSLDQEWYDRGYHGSVSHNARAVLNRYLGYYDGNPATLDPLSPEDSAGRYVEYMGGAERLLEQARASYARGEYRWVVEVVNRLVFAEPDNRAARELQADALEQLGYQAENAGWRNSYLSAAYELRHGVPRDQPTMKAGSADALAAMDTGLLFDYLGVRLDAGAAEGKALSINLRLPDIGENYLLELKNSHLNNLRGVQSEDAGQTVSIDRADLNRLLLKEVSAVRLVFEGKLKSSGNPLLLGQLFGMLGDFDFWFDIVTPAAKSEG",
          "organism": "Pseudomonas aeruginosa",
          "uniprot_code": "Q9I5I9",
          "uniprot_range_first": null,
          "uniprot_range_last": null,
          "oligomerization": "dimer",
          "molecular_type": "protein",
          "uniprot_sequence": "MSRLLALLALAPLLAGAAETTAPKPPSAFTVEAQRRVEAELPFADRADFERADRGLIRRP\nERLLIRNPDGSVAWQLGGYDFLLDGKPRDSINPSLQRQALLNLKYGLFEVAEGIYQVRGF\nDLANITFIRGDSGWIVVDTLTTPATARAAYELVSRELGERPIRTVIYSHAHADHFGGVRG\nLVEPQQVASGAVQIIAPAGFMEAAIKENVLAGNAMMRRATYQYGTQLPKGPQGQVDMAIG\nKGLARGPLSLLAPTRLIEGEGEDLVLDGVPFTFQNTPGTESPAEMNIWLPRQKALLMAEN\nVVGTLHNLYTLRGAEVRDALGWSKYINQALHRFGRQAEVMFAVHNWPRWGNAEIVEVLEK\nQRDLYGYLHDQTLHLANQGVTIGQVHNRLRLPPSLDQEWYDRGYHGSVSHNARAVLNRYL\nGYYDGNPATLDPLSPEDSAGRYVEYMGGAERLLEQARASYARGEYRWVVEVVNRLVFAEP\nDNRAARELQADALEQLGYQAENAGWRNSYLSAAYELRHGVPRDQPTMKAGSADALAAMDT\nGLLFDYLGVRLDAGAAEGKALSINLRLPDIGENYLLELKNSHLNNLRGVQSEDAGQTVSI\nDRADLNRLLLKEVSAVRLVFEGKLKSSGNPLLLGQLFGMLGDFDFWFDIVTPAAKSEG",
          "mw": 72.591,
          "total_mw": 145.183,
          "number_molecules": 2,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
      ],
      "buffer": {
        "name": "50 mM HEPES",
        "concentration_unit": "mM",
        "comment": null,
        "additive": null,
        "concentration": 50.0,
        "pka": null,
        "ph": 7.0,
        "deuteration": null
      },
      "purity_method": null,
      "name": "SDS hydrolase SdsA1",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [],
        "contributor_name": "Eugenio",
        "contributor_surname": "De la Mora",
        "orcid": null
      },
      {
        "affiliation": [],
        "contributor_name": "Dritan",
        "contributor_surname": "Siliqi",
        "orcid": null
      }
    ],
    "concentration_method": null,
    "concentration_unit": "mg/ml",
    "date": "2013-07-22",
    "storage_temperature": 20.0,
    "cell_temperature": null,
    "exposure_time": 30.0,
    "number_of_frames": 6,
    "wavelength": 0.091,
    "sample_detector_distance": 3.4,
    "concentration_min": null,
    "concentration_max": 12.2,
    "sample_volume": null,
    "flow_rate": null,
    "s_min": 0.08,
    "s_max": 19.6,
    "total_exposure_time": null,
    "seccolumn": null
  },
  "fits": [
    {
      "models": [
        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDAC8_fit1_model1_img.png",
          "software": "CRYSOL",
          "pdb_link": [],
          "model_title": null,
          "type_of_model": "atomic",
          "software_version": "",
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDAC8_fit1_model1.pdb",
          "model_mw": 139.5,
          "bead_radius": 1.9,
          "log": null,
          "symmetry": "",
          "comment": "",
          "user": 67
        }
      ],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDAC8_fit1_fit_img.png",
      "software": null,
      "chi_square_value": 7.14,
      "p_value": 0.0,
      "fit_residual_plot": "SASDAC8_fit1_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDAC8_fit1.fit",
      "fit_log": null,
      "software_version": null,
      "description": null
    }
  ],
  "estimated_volume_method": null,
  "pddf_software": "ATSAS GNOM",
  "pddf_software_version": "gnom",
  "i0_calibration_standard": null,
  "description": null,
  "experiment_description": "X-ray synchrotron radiation scattering data from solutions of Pseudomonas aeruginosa SDS \r\nhydrolase SdsA1 in 50 mM HEPES were collected on the X9A camera on the storage ring NSLS \r\n(Brookhaven, USA). Using a 20Hz Pilatus 300K detector  as SAXS detector (located at 3.4m \r\nfrom the sample)  and a custom-designed Photonic Science CCD detector as  WAXS detector \r\n(located at 20cm from the sample).  Together, these two detectors cover a \r\ncombined s range of 0.08 -19.600 nm-1, with overlapping data between 1.2 and  2.0 nm-1 (s = 4π sin θ/λ, where 2θ is the scattering angle). One solute concentration of 12.20 mg/ml \r\nwas measured. Six successive 30 second frames were collected. The data were normalized to \r\nthe intensity of the transmitted beam and radially averaged; the scattering of the \r\nsolvent-blank was subtracted and the different curves were scaled for protein \r\nconcentration. The low angle data collected were obtained from a single concentration \r\nscattering curve.  For SAXS data analysis (RG, Pr function) we used the data up to 2.0 \r\nnm-1.",
  "tags": [
    "waxs"
  ],
  "intensity_unit": null,
  "experimental_mw": 140.0,
  "experimental_mw_error": null,
  "guinier_i0_mw": null,
  "guinier_i0_mw_error": null,
  "porod_mw": 153.0,
  "porod_mw_error": null,
  "pddf_i0": 1607.0,
  "pddf_i0_error": null,
  "guinier_i0": 1590.0,
  "guinier_i0_error": null,
  "pddf_rg": 3.66,
  "pddf_rg_error": null,
  "guinier_rg": 3.6,
  "guinier_rg_error": 0.89,
  "pddf_dmax": 16.9,
  "pddf_dmax_error": null,
  "porod_volume": 261.0,
  "porod_volume_error": null,
  "estimated_volume": null,
  "estimated_volume_error": null,
  "guinier_point_first": null,
  "guinier_point_last": null,
  "pddf_point_first": 11,
  "pddf_point_last": 100,
  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDAC8_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2019-12-06T13:07:15.624532+01:00",
  "bragg_peak": []
}
View the complete manifest.json source
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  "started_at": "2026-08-11T15:50:10.051453+00:00",
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