SASDD52

Arthrospira fluorescence recovery protein AmaxFRP.1-106

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

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 · Arthrospira fluorescence recovery protein AmaxFRP.1-106

浓度— – 5.77 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0.05 s × 20

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Uncharacterized fluorescence recovery protein
查看序列
MSEINWSEQDKNAAVDALHKAYEREVKILIDEVKQKAFNLTEIDEVWKLHDFLSARRHDIDGKYDYRDAASVFVLATLVKQGWLSLEELQVLGQDKLAKISALTRL
proteinArthrospira maxima CS-328B5W3T41–106dimer分子数 212.244 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
11377[3]0.0884003–3.88565 1/nm含误差列缺失 010sasbdb/entries/52/sasdd52/source/SASDD52.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)9.5—nm
i0Guinier0.01613e-051/cm
i0P(r)0.01621—1/cm
mwExperimental22.0—kDa
mwGuinier I(0)22.0—kDa
mwPorod22.0—kDa
porod_volumePorod35.0—nm³
rgGuinier2.680.02nm
rgP(r)2.786—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0.05帧数20
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0.088 – 3.886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/52/sasdd52/source/SASDD52.datdownloaded6231413767a3494b27c0519012197604b883465185ce23846758a715bcf9ffd029bd7下载查看原文件源站
full_entry_zipsasbdb/entries/52/sasdd52/source/SASDD52.zipdownloaded3793391d37f6ed4edc82dc1d7e4aef6a139a8d1556c7728e66848bebc36aa5f25618fb下载查看原文件源站
pddfsasbdb/entries/52/sasdd52/source/SASDD52.outdownloaded1186244540967636ca5b20a66dbbe4cd79cb6a9c537baf67d2dcfe19c84a8223f6a0b2下载查看原文件源站
sascifsasbdb/entries/52/sasdd52/source/SASDD52.sascifdownloaded51405612377279a4ebbfae6cd4ed07d7722dfa4b4dbd200ac44cc71989af977bad9d14下载查看原文件源站
summarysasbdb/entries/52/sasdd52/source/summary.jsondownloaded86914fe421902337b02ea85ce0b9684fad615bfd5bd9b9e1a1f49177fb5d8e5f5a98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:179 个字段值
字段路径原始值
codeSASDD52
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_nameUncharacterized fluorescence recovery protein
experiment.sample.molecule[0].short_nameFRP
experiment.sample.molecule[0].sequenceMSEINWSEQDKNAAVDALHKAYEREVKILIDEVKQKAFNLTEIDEVWKLHDFLSARRHDI DGKYDYRDAASVFVLATLVKQGWLSLEELQVLGQDKLAKISALTRL
experiment.sample.molecule[0].organismArthrospira maxima CS-328
experiment.sample.molecule[0].uniprot_codeB5W3T4
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last106
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeprotein
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experiment.sample.molecule[0].mw12.244
experiment.sample.molecule[0].total_mw24.488
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.nameArthrospira fluorescence recovery protein AmaxFRP.1-106
experiment.sample.ext_coefficientnull
experiment.sample.contrastnull
experiment.sample.specific_volnull
experiment.sample.dry_volnull
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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_time0.05
experiment.number_of_frames20
experiment.wavelength0.124
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experiment.concentration_minnull
experiment.concentration_max5.77
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.088
experiment.s_max3.886
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].chi_square_value1.08
fits[0].p_value0.48876
fits[0].fit_residual_plotSASDD52_fit1_fitresiduals_img.png
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fits[1].models[0].commentFitted using CRYSOL with 25 harmonics, 25 points and constant adjusment.
fits[1].models[0].user9
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fits[1].chi_square_value1.127
fits[1].p_value0.285306
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fits[1].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionAdditional GASBOR models, with spatial alignments and the NSD estimate can be located in the full entry zip archive.
experiment_descriptionSynchrotron SAXS data from solutions of Arthrospira fluorescence recovery protein AmaxFRP.1-106 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). One solute concentration of 5.77 mg/ml was measured at 10°C. 20 successive 0.050 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 data scaled for protein concentration.
tags[]
intensity_unit1/cm
experimental_mw22.0
experimental_mw_errornull
guinier_i0_mw22.0
guinier_i0_mw_errornull
porod_mw22.0
porod_mw_errornull
pddf_i00.01621
pddf_i0_errornull
guinier_i00.0161
guinier_i0_error3e-05
pddf_rg2.786
pddf_rg_errornull
guinier_rg2.68
guinier_rg_error0.02
pddf_dmax9.5
pddf_dmax_errornull
porod_volume35.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last144
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDD52_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
codeSASDD52
statussuccess
started_at2026-08-11T13:30:34.091929+00:00
finished_at2026-08-11T13:30:43.729305+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": "SASDD52",
  "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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    "sample": {
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          "long_name": "Uncharacterized fluorescence recovery protein",
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          "sequence": "MSEINWSEQDKNAAVDALHKAYEREVKILIDEVKQKAFNLTEIDEVWKLHDFLSARRHDI\r\nDGKYDYRDAASVFVLATLVKQGWLSLEELQVLGQDKLAKISALTRL",
          "organism": "Arthrospira maxima CS-328",
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          "uniprot_range_first": 1,
          "uniprot_range_last": 106,
          "oligomerization": "dimer",
          "molecular_type": "protein",
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        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
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        "ph": 7.6,
        "deuteration": null
      },
      "purity_method": null,
      "name": "Arthrospira fluorescence recovery protein AmaxFRP.1-106",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "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_method": null,
    "concentration_unit": null,
    "date": "2017-09-01",
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    "cell_temperature": 10.0,
    "exposure_time": 0.05,
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    "wavelength": 0.124,
    "sample_detector_distance": null,
    "concentration_min": null,
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    "sample_volume": null,
    "flow_rate": null,
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    "s_max": 3.886,
    "total_exposure_time": null,
    "seccolumn": null
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          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDD52_fit1_model1_img.png",
          "software": "GASBOR",
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      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDD52_fit1_fit_img.png",
      "software": "GASBOR",
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      "p_value": 0.48876,
      "fit_residual_plot": "SASDD52_fit1_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDD52_fit1.fir",
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  "intensities_log_log_plot": "SASDD52_datloglog_img.png",
  "symmetry": null,
  "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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