SASDC77

Deoxyuridine 5'-triphosphate nucleotidohydrolase complex with SaPIbov1 pathogenicity island repressor [3:3] (SEC-SAXS)

Data type: SASBDB experimental data Status: Published Curve type: Single concentration Last updated: 2023-06-21T07:56:39.492710+02:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Deoxyuridine 5'-triphosphate nucleotidohydrolase complex with SaPIbov1 pathogenicity island repressor [3:3] (SEC-SAXS)

Concentration— – — Buffer / pH50 mM HEPES 300 mM NaCl 5 mM MgCl2 / 7.5
Experimental temperature10.0 Facility / beamlinePETRA III / EMBL P12
Wavelength0.124 nmExposure1.0 s × 3600

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Deoxyuridine 5'-triphosphate nucleotidohydrolase
View sequence
GSHMPCSEETPAISPSKRARPAEVGGMQLRFARLSEHATAPTRGSARAAGYDLYSAYDYTIPPMEKAVVKTDIQIALPSGCYGRVAPRSGLAAKHFIDVGAGVIDEDYRGNVGVVLFNFGKEKFEVKKGDRIAQLICERIFYPEIEEVQALDDTERGSGGFGSTGKN
proteinHomo sapiensP3331694–252trimerMolecule count 318.029 kDa
SaPIbov1 pathogenicity island repressor
View sequence
GSPEFSMEGAGQMAELPTHYGTIIKTLRKYMKLTQSKLSERTGFSQNTISNHENGNRNIGVNEIEIYGKGLGIPSYILHRISDEFKEKGYSPTLNDFGKFDKMYSYVNKAYYNDGDIYYSSYDLYDETIKLLELLKESKINVNDIDYDYVLKLYKQILSTDTEKSIINYETLANTRKSSDKKREVTIEEIGEFHEKYLKLLFTNLETHNDRKKALAEIEKLKEESIYLGEKLRLVPNHHYDAIKGKPMYKLYLYEYPDRLEHQKKIILEKDTN
proteinStaphylococcus aureusE2FZP613–278dimerMolecule count 232.016 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11799[3]0.0771412–5.0307 1/nmHas uncertainty columnMissing 017sasbdb/entries/77/sasdc77/source/SASDC77.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)17.00.5nm
estimated_volumeDAM volume290.020.0nm³
i0Guinier0.0410.001arbitrary
i0P(r)0.0410.002arbitrary
mwExperimental145.010.0kDa
mwGuinier I(0)145.010.0kDa
mwPorod134.09.0kDa
porod_volumePorod227.010.0nm³
rgGuinier4.360.1nm
rgP(r)4.470.1nm

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 · DAMMIF 2.9.0

χ²: 1.07CorMap p: 0.000554Unit: 1/A
ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—dummyDAMMIF 2.9.0P3147.0—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 name50 mM HEPES 300 mM NaCl 5 mM MgCl2Buffer concentration—
pH7.5Additives—
Buffer descriptionBuffer B
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / 188384Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2016-07-10Storage / measurement temperature10.0 / 10.0
Exposure time1.0Frames3600
Wavelength0.124Sample-to-detector distance3.1
SourceX-ray synchrotronDetectorPilatus 2M
Facility / beamlinePETRA III / EMBL P12 · DESY; Hamburg, Germany
q range0.077 – 5.031Sample 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:196 field values
Field pathRaw value
codeSASDC77
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleStructural model of human dUTPase in complex with a novel proteinaceous inhibitor.
project.publication.titleStructural model of human dUTPase in complex with a novel proteinaceous inhibitor.
project.publication.author_listNyíri K, Mertens HDT, Tihanyi B, Nagy GN, Kőhegyi B, Matejka J, Harris MJ, Szabó JE, Papp-Kádár V, Németh-Pongrácz V, Ozohanics O, Vékey K, Svergun DI, Borysik AJ, Vértessy BG
project.publication.journalSci Rep
project.publication.doi10.1038/s41598-018-22145-8
project.publication.pmid29531348
project.publication.published_date2018 Mar 12
project.statusreleased
project.submitted_date2017-08-10
project.released_date2018-02-27
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experiment.instrument.detector.namePilatus 2M
experiment.instrument.detector.resolutionnull
experiment.instrument.namePETRA III
experiment.instrument.cityDESY; Hamburg
experiment.instrument.countryGermany
experiment.instrument.beamline_nameEMBL P12
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_nameDeoxyuridine 5'-triphosphate nucleotidohydrolase
experiment.sample.molecule[0].short_namehDUT
experiment.sample.molecule[0].sequenceGSHMPCSE ETPAISPSKRARPAEVGGMQLRFARLSEHATAPTRGSARAAGYDLYSAYDYTIPPMEKAVVKTDIQIALPSGCYGRVAPRSGLAAKHFIDVGAGVIDEDYRGNVGVVLFNFGKEKFEVKKGDRIAQLICERIFYPEIEEVQALDDTERGSGGFGSTGKN
experiment.sample.molecule[0].organismHomo sapiens
experiment.sample.molecule[0].uniprot_codeP33316
experiment.sample.molecule[0].uniprot_range_first94
experiment.sample.molecule[0].uniprot_range_last252
experiment.sample.molecule[0].oligomerizationtrimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMTPLCPRPALCYHFLTSLLRSAMQNARGARQRAEAAVLSGPGPPLGRAAQHGIPRPLSSA GRLSQGCRGASTVGAAGWKGELPKAGGSPAPGPETPAISPSKRARPAEVGGMQLRFARLS EHATAPTRGSARAAGYDLYSAYDYTIPPMEKAVVKTDIQIALPSGCYGRVAPRSGLAAKH FIDVGAGVIDEDYRGNVGVVLFNFGKEKFEVKKGDRIAQLICERIFYPEIEEVQALDDTE RGSGGFGSTGKN
experiment.sample.molecule[0].mw18.029
experiment.sample.molecule[0].total_mw54.087
experiment.sample.molecule[0].number_molecules3
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.molecule[1].long_nameSaPIbov1 pathogenicity island repressor
experiment.sample.molecule[1].short_nameStl
experiment.sample.molecule[1].sequenceGSPEFSM EGAGQMAELPTHYGTIIKTLRKYMKLTQSKLSERTGFSQNTISNHENGNRNIGVNEIEIYGKGLGIPSYILHRISDEFKEKGYSPTLNDFGKFDKMYSYVNKAYYNDGDIYYSSYDLYDETIKLLELLKESKINVNDIDYDYVLKLYKQILSTDTEKSIINYETLANTRKSSDKKREVTIEEIGEFHEKYLKLLFTNLETHNDRKKALAEIEKLKEESIYLGEKLRLVPNHHYDAIKGKPMYKLYLYEYPDRLEHQKKIILEKDTN
experiment.sample.molecule[1].organismStaphylococcus aureus
experiment.sample.molecule[1].uniprot_codeE2FZP6
experiment.sample.molecule[1].uniprot_range_first13
experiment.sample.molecule[1].uniprot_range_last278
experiment.sample.molecule[1].oligomerizationdimer
experiment.sample.molecule[1].molecular_typeprotein
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experiment.sample.molecule[1].mw32.016
experiment.sample.molecule[1].total_mw64.032
experiment.sample.molecule[1].number_molecules2
experiment.sample.molecule[1].complex_stateFalse
experiment.sample.molecule[1].deuterationnull
experiment.sample.molecule[1].molecule_sourcebiological
experiment.sample.molecule[1].molecule_descriptionnull
experiment.sample.buffer.name50 mM HEPES 300 mM NaCl 5 mM MgCl2
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentBuffer B
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.nameDeoxyuridine 5'-triphosphate nucleotidohydrolase complex with SaPIbov1 pathogenicity island repressor [3:3] (SEC-SAXS)
experiment.sample.ext_coefficientnull
experiment.sample.contrastnull
experiment.sample.specific_volnull
experiment.sample.dry_vol188384
experiment.sample.absorbptionnull
experiment.sample.deuterationnull
experiment.sample.mixturenull
experiment.contributor[0].affiliation[0].short_nameEMBL-Hamburg
experiment.contributor[0].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[0].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[0].contributor_nameHaydyn
experiment.contributor[0].contributor_surnameMertens
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2016-07-10
experiment.storage_temperature10.0
experiment.cell_temperature10.0
experiment.exposure_time1.0
experiment.number_of_frames3600
experiment.wavelength0.124
experiment.sample_detector_distance3.1
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experiment.concentration_maxnull
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experiment.flow_ratenull
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tags[]
intensity_unitarbitrary
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last_modified2023-06-21T07:56:39.492710+02:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDC77
statussuccess
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View the complete summary.json source
{
  "code": "SASDC77",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
  "project": {
    "title": "Structural model of human dUTPase in complex with a novel proteinaceous inhibitor.",
    "publication": {
      "title": "Structural model of human dUTPase in complex with a novel proteinaceous inhibitor.",
      "author_list": "Nyíri K, Mertens HDT, Tihanyi B, Nagy GN, Kőhegyi B, Matejka J, Harris MJ, Szabó JE, Papp-Kádár V, Németh-Pongrácz V, Ozohanics O, Vékey K, Svergun DI, Borysik AJ, Vértessy BG",
      "journal": "Sci Rep",
      "doi": "10.1038/s41598-018-22145-8",
      "pmid": "29531348",
      "published_date": "2018 Mar 12"
    },
    "status": "released",
    "submitted_date": "2017-08-10",
    "released_date": "2018-02-27"
  },
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View the complete manifest.json source
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