SASDD42

Synechocystis fluorescence recovery protein SynFRP.8-109

Data type: SASBDB experimental data Status: Published Curve type: Single concentration Last updated: 2023-06-21T07:56:39.492710+02:00

The experimental MW quoted above is derived from the average value obtained from MALLS (28 kda), MW from Porod volume (23 kDa), MW from the volume of correlation (23 kDa) and from the method of Fischer et al, SAXSMOW (30 kDa). The hydrodynamic radius obtained from DLS is 2.86 nm. Additional GASBOR models, with spatial alignments and the NSD estimate can be located in the full entry zip archive.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Synechocystis fluorescence recovery protein SynFRP.8-109

Concentration— – 5.0 Buffer / pH20 mM Tris-HCl, 150 mM NaCl, 0.1 mM EDTA, 2 mM dithiothreitol, 3 % v/v glycerol / 7.6
Experimental temperature10.0 Facility / beamlinePETRA III / EMBL P12
Wavelength0.124 nmExposure1.0 s × 3600

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Fluorescence recovery protein
View sequence
PWSQAETQSAHALFRKAYQRELDGLLATVQAQASQITQIDDLWKLHDFLSAKRHEIDGKYDDRQSVIIFVFAQLLKEGLVQAEELTFLAADKQSKIKALARL
proteinSynechocystis sp. PCC 6803P741038–109dimerMolecule count 211.625 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11357[3]0.127035–3.8691 1/nmHas uncertainty columnMissing 016sasbdb/entries/42/sasdd42/source/SASDD42.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)10.5—nm
i0Guinier0.016433e-051/cm
i0P(r)0.01667—1/cm
mwExperimental26.0—kDa
mwGuinier I(0)26.0—kDa
mwPorod23.0—kDa
porod_volumePorod36.0—nm³
rgGuinier2.760.02nm
rgP(r)2.909—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 name20 mM Tris-HCl, 150 mM NaCl, 0.1 mM EDTA, 2 mM dithiothreitol, 3 % v/v glycerolBuffer concentration—
pH7.6Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2017-09-01Storage / measurement temperature10.0 / 10.0
Exposure time1.0Frames3600
Wavelength0.124Sample-to-detector distance—
SourceX-ray synchrotronDetectorPilatus 2M
Facility / beamlinePETRA III / EMBL P12 · DESY; Hamburg, Germany
q range0.127 – 3.869Sample 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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full_entry_zip:source record and ZIP contents (8 items)
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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:182 field values
Field pathRaw value
codeSASDD42
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleFunctional interaction of low-homology FRPs from different cyanobacteria with Synechocystis OCP.
project.publication.titleFunctional interaction of low-homology FRPs from different cyanobacteria with Synechocystis OCP.
project.publication.author_listSlonimskiy YB, Maksimov EG, Lukashev EP, Moldenhauer M, Jeffries CM, Svergun DI, Friedrich T, Sluchanko NN
project.publication.journalBiochim Biophys Acta
project.publication.doi10.1016/j.bbabio.2018.03.001
project.publication.pmid29524381
project.publication.published_date2018 May
project.statusreleased
project.submitted_datenull
project.released_date2018-03-10
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experiment.instrument.detector.typenull
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_nameFluorescence recovery protein
experiment.sample.molecule[0].short_nameFRP
experiment.sample.molecule[0].sequencePWSQAETQSAHALFRKAYQRELDGLLATVQAQASQITQIDDLWKLHDFLSAKR HEIDGKYDDRQSVIIFVFAQLLKEGLVQAEELTFLAADKQSKIKALARL
experiment.sample.molecule[0].organismSynechocystis sp. PCC 6803
experiment.sample.molecule[0].uniprot_codeP74103
experiment.sample.molecule[0].uniprot_range_first8
experiment.sample.molecule[0].uniprot_range_last109
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMLQTAEAPWSQAETQSAHALFRKAYQRELDGLLATVQAQASQITQIDDLWKLHDFLSAKR HEIDGKYDDRQSVIIFVFAQLLKEGLVQAEELTFLAADKQSKIKALARL
experiment.sample.molecule[0].mw11.625
experiment.sample.molecule[0].total_mw23.25
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.name20 mM Tris-HCl, 150 mM NaCl, 0.1 mM EDTA, 2 mM dithiothreitol, 3 % v/v glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.6
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameSynechocystis fluorescence recovery protein SynFRP.8-109
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_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_nameCy M
experiment.contributor[0].contributor_surnameJeffries
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2017-09-01
experiment.storage_temperature10.0
experiment.cell_temperature10.0
experiment.exposure_time1.0
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experiment.flow_ratenull
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fits[0].chi_square_value1.15
fits[0].p_value0.735192
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fits[1].p_value0.00032
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fits[1].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionThe experimental MW quoted above is derived from the average value obtained from MALLS (28 kda), MW from Porod volume (23 kDa), MW from the volume of correlation (23 kDa) and from the method of Fischer et al, SAXSMOW (30 kDa). The hydrodynamic radius obtained from DLS is 2.86 nm. Additional GASBOR models, with spatial alignments and the NSD estimate can be located in the full entry zip archive.
experiment_descriptionSize-exclusion chromatography SAXS (SEC-SAXS) data from solutions of Synechocystis fluorescence recovery protein SynFRP.8-109 in 20 mM Tris-HCl, 150 mM NaCl, 0.1 mM EDTA, 2 mM dithiothreitol, 3 % v/v glycerol, pH 7.6 were collected at the EMBL-P12 bioSAXS beam line at the PETRA III storage ring (Hamburg, Germany) using a Pilatus 2M detector at a wavelength of λ = 0.124 nm (I(s) vs s, where s = 4πsinθ/λ and 2θ is the scattering angle). 100 μl of sample at 5.00 mg/ml were loaded on a Superdex 200 Increase 10/300 column (GE Healthcare) at a flow rate of 0.5 ml/min. 3600 successive 1 second frames were collected from the column eluate that were additionally analyzed using multi-angle laser light scattering (MALLS), refractive index (RI) and and dynamic light scattering (DLS) measurements. The SAXS data were processed using the software CHROMIXS as part of the ATSAS 2.8.3 SAS data analysis package.
tags[]
intensity_unit1/cm
experimental_mw26.0
experimental_mw_errornull
guinier_i0_mw26.0
guinier_i0_mw_errornull
porod_mw23.0
porod_mw_errornull
pddf_i00.01667
pddf_i0_errornull
guinier_i00.01643
guinier_i0_error3e-05
pddf_rg2.909
pddf_rg_errornull
guinier_rg2.76
guinier_rg_error0.02
pddf_dmax10.5
pddf_dmax_errornull
porod_volume36.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last125
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDD42_datloglog_img.png
symmetrynull
last_modified2023-06-21T07:56:39.492710+02:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDD42
statussuccess
started_at2026-08-11T13:29:53.159207+00:00
finished_at2026-08-11T13:30:03.260883+00:00
source_last_modified2023-06-21T07:56:39.492710+02:00
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View the complete summary.json source
{
  "code": "SASDD42",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
  "project": {
    "title": "Functional interaction of low-homology FRPs from different cyanobacteria with Synechocystis OCP.",
    "publication": {
      "title": "Functional interaction of low-homology FRPs from different cyanobacteria with Synechocystis OCP.",
      "author_list": "Slonimskiy YB, Maksimov EG, Lukashev EP, Moldenhauer M, Jeffries CM, Svergun DI, Friedrich T, Sluchanko NN",
      "journal": "Biochim Biophys Acta",
      "doi": "10.1016/j.bbabio.2018.03.001",
      "pmid": "29524381",
      "published_date": "2018 May"
    },
    "status": "released",
    "submitted_date": null,
    "released_date": "2018-03-10"
  },
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      "xray_energy": null,
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    },
    "sample": {
      "molecule": [
        {
          "long_name": "Fluorescence recovery protein",
          "short_name": "FRP",
          "sequence": "PWSQAETQSAHALFRKAYQRELDGLLATVQAQASQITQIDDLWKLHDFLSAKR\r\nHEIDGKYDDRQSVIIFVFAQLLKEGLVQAEELTFLAADKQSKIKALARL",
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          "uniprot_code": "P74103",
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          "oligomerization": "dimer",
          "molecular_type": "protein",
          "uniprot_sequence": "MLQTAEAPWSQAETQSAHALFRKAYQRELDGLLATVQAQASQITQIDDLWKLHDFLSAKR\nHEIDGKYDDRQSVIIFVFAQLLKEGLVQAEELTFLAADKQSKIKALARL",
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          "molecule_source": "biological",
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      ],
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      "name": "Synechocystis fluorescence recovery protein SynFRP.8-109",
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      "contrast": null,
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      "dry_vol": null,
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      "deuteration": null,
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    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": "EMBL-Hamburg",
            "address": "Notkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany",
            "full_name": "European Molecular Biology Laboratory (EMBL) - Hamburg outstation",
            "webpage": "http://www.embl-hamburg.de/index.php"
          }
        ],
        "contributor_name": "Cy M",
        "contributor_surname": "Jeffries",
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    "concentration_unit": null,
    "date": "2017-09-01",
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  "last_modified": "2023-06-21T07:56:39.492710+02:00",
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}
View the complete manifest.json source
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