SASDGD5

The PDZ1-2 domain of postsynaptic density protein 95 (PSD-95) bound to RRESEI peptide (Paused SEC)

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2019-12-06T13:07:15.624532+01:00

Scattering data are fitted using the ATSAS OLIGOMER program using a suite of models. The ATSAS program FFMAKER was used to generate form factors for each model in the suite. Each model is assigned a volume fraction to fit the observed scattering profile. 3 monomer models are included, the first is a compact conformation of PDZ1-2 similar to PDB entries 6spv/6spz; the other two are domain models obtained from a representative run of the ATSAS EOM program with data projected to infinite dilution. Multimeric models are drawn from a "clustering Spacegroup", unit cell 14.8nm symmetry I2(1)3, and consist of identical copies of an extended conformation of PDZ1-2 (similar to PDB entry 3zrt) assembled by symmetry operations. In the order of deposition: Model number; Stoichiometry; MW (kDa); source; Volume fraction. 1; 1; 21; Crystal Structure; 0.381. 2; 1; 21; EOM; 0.091. 3; 1; 21; EOM; 0.470. 4; 2; 42; clustering Spacegroup; 0.042. 5; 4; 84; clustering Spacegroup; 0.015. 6; 8; 168; clustering Spacegroup; 0.000. 7; 12, 252; clustering Spacegroup; 0.001. 8; 16, 336, clustering Spacegroup; 0.000. 9; 20, 420, clustering Spacegroup; 0.000. 10; 24, 504, clustering Spacegroup; 0.001.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · The PDZ1-2 domain of postsynaptic density protein 95 (PSD-95) bound to RRESEI peptide (Paused SEC)

Concentration— – 15.0 Buffer / pH20 mM TRIS/HCl, 150 mM NaCl + 10 mM RRESEI / 8.5
Experimental temperature— Facility / beamlineDiamond Light Source / B21
Wavelength0.1 nmExposure10.0 s × 69

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
PDZ1-2 fragment of PSD-95/Disks large homolog 4
View sequence
GPGTEGEMEYEEITLERGNSGLGFSIAGGTDNPHIGDDPSIFITKIIPGGAAAQDGRLRVNDSILFVNEVDVREVTHSAAVEALKEAGSIVRLYVMRRKPPAEKVMEIKLIKGPKGLGFSIAGGVGNQHIPGDNSIYVTKIIEGGAAHKDGRLQIGDKILAVNSVGLEDVMHEDAVAALKNTYDVVYLKVAKPSNA
proteinHomo sapiensP7835255–249monomerMolecule count 120.8 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11393[3]0.0171143–0.399735 1/AHas uncertainty columnMissing 00sasbdb/entries/d5/sasdgd5/source/SASDGD5.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)6.84—Å
i0Guinier0.00950.0001arbitrary
i0P(r)0.009483—arbitrary
mwExperimental20.8—kDa
mwPorod18.0—kDa
porod_volumePorod28.0—ų
rgGuinier2.3340.072Å
rgP(r)2.34—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 · OLIGOMER

χ²: 3.71CorMap p: 0.0Unit: 1/A
ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—atomicOther —21.7—Model Image
2—atomicOther —21.12—Model Image
3—atomicOther —21.12—Model Image
4—atomicOther —43.02—Model Image
5—atomicOther —86.04—Model Image
6—atomicOther —172.1—Model Image
7—atomicOther —258.1—Model Image
8—atomicOther —344.2—Model Image
9—atomicOther —430.2—Model Image
10—atomicOther —516.2—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 name20 mM TRIS/HCl, 150 mM NaCl + 10 mM RRESEIBuffer concentration—
pH8.5Additives—
Buffer descriptionstandard buffer plus 10mM ligand peptide
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2016-01-26Storage / measurement temperature— / —
Exposure time10.0Frames69
Wavelength0.1Sample-to-detector distance3.9
SourceX-ray synchrotronDetectorPilatus 2M
Facility / beamlineDiamond Light Source / B21 · Didcot, UK
q range0.171 – 3.997Sample volume / flow rate20.0 / 0.0

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:273 field values
Field pathRaw value
codeSASDGD5
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleThe dual PDZ domain from Postsynaptic density protein 95 forms a scaffold with peptide ligand
project.publication.titleThe dual PDZ domain from Postsynaptic density protein 95 forms a scaffold with peptide ligand
project.publication.author_listRodzli N, Lockhart-Cairns M, Levy C, Chipperfield J, Bird L, Baldock C, Prince S
project.publication.journalBiophysical Journal
project.publication.doi10.1016/j.bpj.2020.06.018
project.publication.pmidnull
project.publication.published_date2020 Jun
project.statusreleased
project.submitted_date2019-09-16
project.released_date2019-09-20
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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_namePDZ1-2 fragment of PSD-95/Disks large homolog 4
experiment.sample.molecule[0].short_namePDZ1-2
experiment.sample.molecule[0].sequenceGPGTEGEMEYEEITLERGNSGLGFSIAGGTDNPHIGDDPSIFITKIIPGGAAAQDGRLRV NDSILFVNEVDVREVTHSAAVEALKEAGSIVRLYVMRRKPPAEKVMEIKLIKGPKGLGFS IAGGVGNQHIPGDNSIYVTKIIEGGAAHKDGRLQIGDKILAVNSVGLEDVMHEDAVAALK NTYDVVYLKVAKPSNA
experiment.sample.molecule[0].organismHomo sapiens
experiment.sample.molecule[0].uniprot_codeP78352
experiment.sample.molecule[0].uniprot_range_first55
experiment.sample.molecule[0].uniprot_range_last249
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMDCLCIVTTKKYRYQDEDTPPLEHSPAHLPNQANSPPVIVNTDTLEAPGYELQVNGTEGE MEYEEITLERGNSGLGFSIAGGTDNPHIGDDPSIFITKIIPGGAAAQDGRLRVNDSILFV NEVDVREVTHSAAVEALKEAGSIVRLYVMRRKPPAEKVMEIKLIKGPKGLGFSIAGGVGN QHIPGDNSIYVTKIIEGGAAHKDGRLQIGDKILAVNSVGLEDVMHEDAVAALKNTYDVVY LKVAKPSNAYLSDSYAPPDITTSYSQHLDNEISHSSYLGTDYPTAMTPTSPRRYSPVAKD LLGEEDIPREPRRIVIHRGSTGLGFNIVGGEDGEGIFISFILAGGPADLSGELRKGDQIL SVNGVDLRNASHEQAAIALKNAGQTVTIIAQYKPEEYSRFEAKIHDLREQLMNSSLGSGT ASLRSNPKRGFYIRALFDYDKTKDCGFLSQALSFRFGDVLHVIDASDEEWWQARRVHSDS ETDDIGFIPSKRRVERREWSRLKAKDWGSSSGSQGREDSVLSYETVTQMEVHYARPIIIL GPTKDRANDDLLSEFPDKFGSCVPHTTRPKREYEIDGRDYHFVSSREKMEKDIQAHKFIE AGQYNSHLYGTSVQSVREVAEQGKHCILDVSANAVRRLQAAHLHPIAIFIRPRSLENVLE INKRITEEQARKAFDRATKLEQEFTECFSAIVEGDSFEEIYHKVKRVIEDLSGPYIWVPA RERL
experiment.sample.molecule[0].mw20.8
experiment.sample.molecule[0].total_mw20.8
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.name20 mM TRIS/HCl, 150 mM NaCl + 10 mM RRESEI
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentstandard buffer plus 10mM ligand peptide
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph8.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameThe PDZ1-2 domain of postsynaptic density protein 95 (PSD-95) bound to RRESEI peptide (Paused SEC)
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].addressManchester, UK
experiment.contributor[0].affiliation[0].full_nameUniversity of Manchester
experiment.contributor[0].affiliation[0].webpagehttp://www.manchester.ac.uk/
experiment.contributor[0].contributor_nameStephen
experiment.contributor[0].contributor_surnamePrince
experiment.contributor[0].orcidhttps://orcid.org/0000-0003-0929-0254
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2016-01-26
experiment.storage_temperaturenull
experiment.cell_temperaturenull
experiment.exposure_time10.0
experiment.number_of_frames69
experiment.wavelength0.1
experiment.sample_detector_distance3.9
experiment.concentration_minnull
experiment.concentration_max15.0
experiment.sample_volume20.0
experiment.flow_rate0.0
experiment.s_min0.171
experiment.s_max3.997
experiment.total_exposure_timenull
experiment.seccolumn19
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