SASDD42

Synechocystis fluorescence recovery protein SynFRP.8-109

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新: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. 样品、组分与实验条件 Sample & Experiment

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

浓度— – 5.0 缓冲液 / pH20 mM Tris-HCl, 150 mM NaCl, 0.1 mM EDTA, 2 mM dithiothreitol, 3 % v/v glycerol / 7.6
实验温度10.0 设备 / 束线PETRA III / EMBL P12
波长0.124 nm曝光1.0 s × 3600

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Fluorescence recovery protein
查看序列
PWSQAETQSAHALFRKAYQRELDGLLATVQAQASQITQIDDLWKLHDFLSAKRHEIDGKYDDRQSVIIFVFAQLLKEGLVQAEELTFLAADKQSKIKALARL
proteinSynechocystis sp. PCC 6803P741038–109dimer分子数 211.625 kDa

实验曲线

曲线点数 / 列q 范围误差质量负强度点来源文件
11357[3]0.127035–3.8691 1/nm含误差列缺失 016sasbdb/entries/42/sasdd42/source/SASDD42.dat
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2. SASBDB 报告的指标 Reported Results

指标方法数值误差单位
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

这些数值是 SASBDB 来源记录,不是 SAXSdb 对实验曲线重新计算的结果。

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3. 来源拟合与模型 Source Fits & Models

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4. 来源文件索引 Source Files

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5. 实验说明与论文 Experiment & Publication

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6. 完整来源记录 Complete Source Record

下列内容直接来自 SASBDB 条目。字段没有值时显示“—”;未声明的单位不会由 SAXSdb 猜测。

打开 SASBDB 原始条目

缓冲液与样品属性

缓冲液名称20 mM Tris-HCl, 150 mM NaCl, 0.1 mM EDTA, 2 mM dithiothreitol, 3 % v/v glycerol缓冲液浓度—
pH7.6添加剂—
缓冲液说明—
纯度测定方法—消光系数—
吸收值—散射对比度—
比体积 / 干体积— / —混合物 / 氘代— / —

采集条件与仪器

测量日期2017-09-01储存 / 测量温度10.0 / 10.0
曝光时间1.0帧数3600
波长0.124样品-探测器距离—
光源X-ray synchrotron探测器Pilatus 2M
机构 / 束线PETRA III / EMBL P12 · DESY; Hamburg, Germany
q 范围0.127 – 3.869样品体积 / 流速— / —

SASBDB 原始图

实验 I(q)
实验 I(q)
实验 I(q) log-log
实验 I(q) log-log
Guinier 图
Guinier 图
Kratky 图
Kratky 图
P(r) 图
P(r) 图

可下载文件

类别文件状态大小校验值下载与查看
curvesasbdb/entries/42/sasdd42/source/SASDD42.datdownloaded6141491c54437b2af3e4031bb05a7d25d23b84ce01f59af76ed8bb1ffada59776f8d6下载查看原文件源站
full_entry_zipsasbdb/entries/42/sasdd42/source/SASDD42.zipdownloaded370394bed7570b74568e25bef37f7e6a58a89b76983a3ab52174a245d983d2063626ff下载查看原文件源站
pddfsasbdb/entries/42/sasdd42/source/SASDD42.outdownloaded117164c99120c537b4da2b60e365fe5566378d770925f1ad09f1d8a8af14175f3efb8c下载查看原文件源站
sascifsasbdb/entries/42/sasdd42/source/SASDD42.sascifdownloaded4997063200a0b227a338fbbe4df8230a2d556172b82c457998452133d8c6ac036ca036下载查看原文件源站
summarysasbdb/entries/42/sasdd42/source/summary.jsondownloaded937220b52204468d256b3acdb0a974072e8b4e26c2a97578dc6936a7ca9b3898e6cf下载查看原文件源站
curve:来源记录
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full_entry_zip:来源记录与 ZIP 内部目录(8 项)
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pddf:来源记录
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sascif:来源记录
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summary:来源记录
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全部来源字段(无筛选)

这里自动展开来源记录中的每一个字段,包括空值、列表成员和页面上方已展示过的字段。

summary.json:182 个字段值
字段路径原始值
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
experiment.number_of_frames3600
experiment.wavelength0.124
experiment.sample_detector_distancenull
experiment.concentration_minnull
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experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.127
experiment.s_max3.869
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].chi_square_value1.15
fits[0].p_value0.735192
fits[0].fit_residual_plotSASDD42_fit1_fitresiduals_img.png
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fits[1].models[0].bead_radius1.9
fits[1].models[0].lognull
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fits[1].chi_square_value1.387
fits[1].p_value0.00032
fits[1].fit_residual_plotSASDD42_fit2_fitresiduals_img.png
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fits[1].software_version2.8.3
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 个字段值
字段路径原始值
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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查看完整 summary.json 原文
{
  "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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  "experiment": {
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        "name": "Pilatus 2M",
        "resolution": null
      },
      "name": "PETRA III",
      "city": "DESY; Hamburg",
      "country": "Germany",
      "beamline_name": "EMBL P12",
      "beam_geometry": null,
      "type_of_source": "X-ray synchrotron",
      "point_source": null,
      "line_collimation": null,
      "sample_path_length": null,
      "line_collimation_slitlength": null,
      "line_collimation_integrationwidth": null,
      "xray_energy": null,
      "beam_profile_ah": null,
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          "organism": "Synechocystis sp. PCC 6803",
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          "uniprot_range_first": 8,
          "uniprot_range_last": 109,
          "oligomerization": "dimer",
          "molecular_type": "protein",
          "uniprot_sequence": "MLQTAEAPWSQAETQSAHALFRKAYQRELDGLLATVQAQASQITQIDDLWKLHDFLSAKR\nHEIDGKYDDRQSVIIFVFAQLLKEGLVQAEELTFLAADKQSKIKALARL",
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          "deuteration": null,
          "molecule_source": "biological",
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      "name": "Synechocystis fluorescence recovery protein SynFRP.8-109",
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      "contrast": null,
      "specific_vol": null,
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      "absorbption": null,
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      "mixture": 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",
        "orcid": null
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    "concentration_unit": null,
    "date": "2017-09-01",
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    "cell_temperature": 10.0,
    "exposure_time": 1.0,
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    "wavelength": 0.124,
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    "concentration_min": null,
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          "type_of_model": "dummy",
          "software_version": "2.3i",
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDD42_fit1_model1.pdb",
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      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDD42_fit1_fit_img.png",
      "software": "GASBOR",
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      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDD42_fit1.fir",
      "fit_log": "https://www.sasbdb.org/media/fitting_files/log_files/Syn2.log",
      "software_version": "2.3i",
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  "experiment_description": "Size-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.",
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  "last_modified": "2023-06-21T07:56:39.492710+02:00",
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}
查看完整 manifest.json 原文
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