SASDBT7

Nucleosome Core Particle: 1.9 M NaCl, 50% sucrose, 50ms - 10s time resolved data

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2019-12-06T13:07:15.624532+01:00

From the depositor: "Protein signal is blanked out in 50% sucrose, only DNA contributes to the scattering. Hence, the SAXS profile reports the Rg and molecule weight of the DNA in the nucleosome core particle complex."

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Nucleosome Core Particle: 1.9 M NaCl, 50% sucrose, 50ms - 10s time resolved data

浓度— – 2.0 缓冲液 / pH20 mM Tris-Cl, 0.1 mM EDTA, 0.1 mM DTT, 50% sucrose, 1.9 M NaCl / 7.5
实验温度20.0 设备 / 束线Advanced Photon Source (APS), Argonne National Laboratory / BioCAT 18ID
波长0.125 nm曝光0.01 s × 5

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Nucleasome Core Particle with Widom 601 DNA - HISTONE H2A-H2B Heterodimer
查看序列
GKQGGKTRAKAKTRSSRAGLQFPVGRVHRLLRKGNYAERVGAGAPVYLAAVLEYLTAEILELAGNAARDNKKTRIIPRHLQLAVRNDEELNKLLGRVTIAQGGVLPNIQSVLLPKKKKRRKTRKESYAIYVYKVLKQVHPDTGISSKAMSIMNSFVNDVFERIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVTKYTSAK
proteinXenopus laevis——–—dimer分子数 223.754 kDa
Nucleasome Core Particle with Widom 601 DNA - HISTONE H3-H4 Heterodimer
查看序列
LATKAARKSAPATGGVKKPHRYRPGTVALREIRRYQKSTELLIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEASEAYLVALFEDTNLCAIHAKRVTIMPKDIQLARRIRGERAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLKVFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
proteinXenopus laevis——–—dimer分子数 223.168 kDa
Nucleasome Core Particle with Widom 601 DNA - dsDNA
查看序列
ATCGGGATGTATATATCTGACACGTGCCTGGAGACTAGGGAGTAATCCCCTTGGCGGTTAAAACGCGGGGGACAGCGCGTACGTGCGTTTAAGCGGTGCTAGAGCTGTCTACGACCAATTGAGCGGCCTCGGCACCGGGATTCTCCGATATCGGAGAATCCCGGTGCCGAGGCCGCTCAATTGGTCGTAGACAGCTCTAGCACCGCTTAAACGCACGTACGCGCTGTCCCCCGCGTTTTAACCGCCAAGGGGATTACTCCCTAGTCTCCAGGCACGTGTCAGATATATACATCCCGAT
DNAXenopus laevis——–—monomer分子数 192.093 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
1127[3]0.006–0.195 1/A含误差列缺失 030sasbdb/entries/t7/sasdbt7/source/SASDBT7.dat
▼

2. SASBDB 报告的指标 Reported Results

指标方法数值误差单位
i0Guinier146000.010100.0—
mwExperimental186.0—kDa
mwGuinier I(0)80.952.8kDa
rgGuinier6.780.641Å

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

该条目没有来源拟合记录。

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4. 来源文件索引 Source Files

▶

5. 实验说明与论文 Experiment & Publication

▼

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-Cl, 0.1 mM EDTA, 0.1 mM DTT, 50% sucrose, 1.9 M NaCl缓冲液浓度—
pH7.5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2014-04-14储存 / 测量温度0.0 / 20.0
曝光时间0.01帧数5
波长0.125样品-探测器距离2.5
光源X-ray synchrotron探测器Pilatus 100K
机构 / 束线Advanced Photon Source (APS), Argonne National Laboratory / BioCAT 18ID · Lemont, IL, USA
q 范围0.06 – 1.95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

可下载文件

类别文件状态大小校验值下载与查看
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full_entry_zipsasbdb/entries/t7/sasdbt7/source/SASDBT7.zipdownloaded231524c420dc2b1d8b0feaf318642e80f29ff64940a10ec4126a72e92797c5b923444下载查看原文件源站
pddfsasbdb/entries/t7/sasdbt7/source/SASDBT7.outnot_listed——下载查看原文件
sascifsasbdb/entries/t7/sasdbt7/source/SASDBT7.sascifdownloaded13622778105b65bf93b2705deb320088715952e62a64d67586af77e120f188704ab5d下载查看原文件源站
summarysasbdb/entries/t7/sasdbt7/source/summary.jsondownloaded8263f8e15cc3b9a6bd0296c02cad46ed1e95d08af859251a52d6d97acf8b89494819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(3 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:168 个字段值
字段路径原始值
codeSASDBT7
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleAsymmetric unwrapping of nucleosomal DNA propagates asymmetric opening and dissociation of the histone core.
project.publication.titleAsymmetric unwrapping of nucleosomal DNA propagates asymmetric opening and dissociation of the histone core.
project.publication.author_listChen Y, Tokuda JM, Topping T, Meisburger SP, Pabit SA, Gloss LM, Pollack L
project.publication.journalProc Natl Acad Sci U S A
project.publication.doi10.1073/pnas.1611118114
project.publication.pmid28028239
project.publication.published_date2017 Jan 10
project.statusreleased
project.submitted_date2016-10-27
project.released_date2017-02-15
pddf_datanull
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDBT7.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDBT7_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDBT7_kratky_img.png
pddf_plotnull
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDBT7_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDBT7.sascif
experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus 100K
experiment.instrument.detector.resolution172.0
experiment.instrument.nameAdvanced Photon Source (APS), Argonne National Laboratory
experiment.instrument.cityLemont, IL
experiment.instrument.countryUSA
experiment.instrument.beamline_nameBioCAT 18ID
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_nameNucleasome Core Particle with Widom 601 DNA - HISTONE H2A-H2B Heterodimer
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceGKQGGKTRAKAKTRSSRAGLQFPVGRVHRLLRKGNYAERVGAGAPVYLAAVLEYLTAEILELAGNAARDNKKTRIIPRHLQLAVRNDEELNKLLGRVTIAQGGVLPNIQSVLLPKK KKRRKTRKESYAIYVYKVLKQVHPDTGISSKAMSIMNSFVNDVFERIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVTKYTSAK
experiment.sample.molecule[0].organismXenopus laevis
experiment.sample.molecule[0].uniprot_codenull
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequencenull
experiment.sample.molecule[0].mw23.754
experiment.sample.molecule[0].total_mw47.508
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.molecule[1].long_nameNucleasome Core Particle with Widom 601 DNA - HISTONE H3-H4 Heterodimer
experiment.sample.molecule[1].short_namenull
experiment.sample.molecule[1].sequenceLATKAARKSAPATGGVKKPHRYRPGTVALREIRRYQKSTELLIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEASEAYLVALFEDTNLCAIHAKRVTIMPKDIQLARRIRGERA KRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLKVFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
experiment.sample.molecule[1].organismXenopus laevis
experiment.sample.molecule[1].uniprot_codenull
experiment.sample.molecule[1].uniprot_range_firstnull
experiment.sample.molecule[1].uniprot_range_lastnull
experiment.sample.molecule[1].oligomerizationdimer
experiment.sample.molecule[1].molecular_typeprotein
experiment.sample.molecule[1].uniprot_sequencenull
experiment.sample.molecule[1].mw23.168
experiment.sample.molecule[1].total_mw46.336
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.molecule[2].long_nameNucleasome Core Particle with Widom 601 DNA - dsDNA
experiment.sample.molecule[2].short_namenull
experiment.sample.molecule[2].sequenceATCGGGATGTATATATCTGACACGTGCCTGGAGACTAGGGAGTAATCCCCTTGGCGGTTAAAACGCGGGGGACAGCGCGTACGTGCGTTTAAGCGGTGCTAGAGCTGTCTACGACCAATTGAGCGGCCTCGGCACCGGGATTCTCCGAT ATCGGAGAATCCCGGTGCCGAGGCCGCTCAATTGGTCGTAGACAGCTCTAGCACCGCTTAAACGCACGTACGCGCTGTCCCCCGCGTTTTAACCGCCAAGGGGATTACTCCCTAGTCTCCAGGCACGTGTCAGATATATACATCCCGAT
experiment.sample.molecule[2].organismXenopus laevis
experiment.sample.molecule[2].uniprot_codenull
experiment.sample.molecule[2].uniprot_range_firstnull
experiment.sample.molecule[2].uniprot_range_lastnull
experiment.sample.molecule[2].oligomerizationmonomer
experiment.sample.molecule[2].molecular_typeDNA
experiment.sample.molecule[2].uniprot_sequencenull
experiment.sample.molecule[2].mw92.093
experiment.sample.molecule[2].total_mw92.093
experiment.sample.molecule[2].number_molecules1
experiment.sample.molecule[2].complex_stateFalse
experiment.sample.molecule[2].deuterationnull
experiment.sample.molecule[2].molecule_sourcebiological
experiment.sample.molecule[2].molecule_descriptionnull
experiment.sample.buffer.name20 mM Tris-Cl, 0.1 mM EDTA, 0.1 mM DTT, 50% sucrose, 1.9 M NaCl
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameNucleosome Core Particle: 1.9 M NaCl, 50% sucrose, 50ms - 10s time resolved data
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].addressIthaca, NY, United States
experiment.contributor[0].affiliation[0].full_nameCornell University
experiment.contributor[0].affiliation[0].webpagehttps://www.cornell.edu/
experiment.contributor[0].contributor_nameYujie
experiment.contributor[0].contributor_surnameChen
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2014-04-14
experiment.storage_temperature0.0
experiment.cell_temperature20.0
experiment.exposure_time0.01
experiment.number_of_frames5
experiment.wavelength0.125
experiment.sample_detector_distance2.5
experiment.concentration_minnull
experiment.concentration_max2.0
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.06
experiment.s_max1.95
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[]
estimated_volume_methodnull
pddf_softwarenull
pddf_software_versionnull
i0_calibration_standardnull
descriptionFrom the depositor: "Protein signal is blanked out in 50% sucrose, only DNA contributes to the scattering. Hence, the SAXS profile reports the Rg and molecule weight of the DNA in the nucleosome core particle complex."
experiment_descriptionSynchrotron SAXS data from solutions of Nucleosome Core Particle in 20 mM Tris-Cl, 0.1 mM EDTA, 0.1 mM DTT, 50% sucrose, 1.9 M NaCl, pH 7.5 were collected on the 18ID beam line at the Advanced Photon Source (APS), Argonne National Laboratory (Lemont, IL, USA) using a Pilatus 100K detector at a sample-detector distance of 2.5 m and at a wavelength of λ = 0.125 nm (I(s) vs s, where s = 4π sin θ/λ and 2θ is the scattering angle). One solute concentration of 2.00 mg/ml was measured at 20°C through a time-course spanning 50 ms to 10 s (with a 50 ms delay time). The data displayed in this entry represent the scattering after 50 ms; the remaining data from the time series can be located in the full-entry zip archive.
tags[]
intensity_unitnull
experimental_mw186.0
experimental_mw_errornull
guinier_i0_mw80.95
guinier_i0_mw_error2.8
porod_mwnull
porod_mw_errornull
pddf_i0null
pddf_i0_errornull
guinier_i0146000.0
guinier_i0_error10100.0
pddf_rgnull
pddf_rg_errornull
guinier_rg6.78
guinier_rg_error0.641
pddf_dmaxnull
pddf_dmax_errornull
porod_volumenull
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last10
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDBT7_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:33 个字段值
字段路径原始值
codeSASDBT7
statussuccess
started_at2026-08-11T15:38:35.904912+00:00
finished_at2026-08-11T15:38:41.370132+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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查看完整 summary.json 原文
{
  "code": "SASDBT7",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Asymmetric unwrapping of nucleosomal DNA propagates asymmetric opening and dissociation of the histone core.",
    "publication": {
      "title": "Asymmetric unwrapping of nucleosomal DNA propagates asymmetric opening and dissociation of the histone core.",
      "author_list": "Chen Y, Tokuda JM, Topping T, Meisburger SP, Pabit SA, Gloss LM, Pollack L",
      "journal": "Proc Natl Acad Sci U S A",
      "doi": "10.1073/pnas.1611118114",
      "pmid": "28028239",
      "published_date": "2017 Jan 10"
    },
    "status": "released",
    "submitted_date": "2016-10-27",
    "released_date": "2017-02-15"
  },
  "pddf_data": null,
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          "short_name": null,
          "sequence": "GKQGGKTRAKAKTRSSRAGLQFPVGRVHRLLRKGNYAERVGAGAPVYLAAVLEYLTAEILELAGNAARDNKKTRIIPRHLQLAVRNDEELNKLLGRVTIAQGGVLPNIQSVLLPKK\r\n\r\nKKRRKTRKESYAIYVYKVLKQVHPDTGISSKAMSIMNSFVNDVFERIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVTKYTSAK",
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          "oligomerization": "dimer",
          "molecular_type": "protein",
          "uniprot_sequence": null,
          "mw": 23.754,
          "total_mw": 47.508,
          "number_molecules": 2,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        },
        {
          "long_name": "Nucleasome Core Particle with Widom 601 DNA - HISTONE H3-H4 Heterodimer",
          "short_name": null,
          "sequence": "LATKAARKSAPATGGVKKPHRYRPGTVALREIRRYQKSTELLIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEASEAYLVALFEDTNLCAIHAKRVTIMPKDIQLARRIRGERA\r\n\r\nKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLKVFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG",
          "organism": "Xenopus laevis",
          "uniprot_code": null,
          "uniprot_range_first": null,
          "uniprot_range_last": null,
          "oligomerization": "dimer",
          "molecular_type": "protein",
          "uniprot_sequence": null,
          "mw": 23.168,
          "total_mw": 46.336,
          "number_molecules": 2,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        },
        {
          "long_name": "Nucleasome Core Particle with Widom 601 DNA - dsDNA",
          "short_name": null,
          "sequence": "ATCGGGATGTATATATCTGACACGTGCCTGGAGACTAGGGAGTAATCCCCTTGGCGGTTAAAACGCGGGGGACAGCGCGTACGTGCGTTTAAGCGGTGCTAGAGCTGTCTACGACCAATTGAGCGGCCTCGGCACCGGGATTCTCCGAT\r\n \r\n\r\nATCGGAGAATCCCGGTGCCGAGGCCGCTCAATTGGTCGTAGACAGCTCTAGCACCGCTTAAACGCACGTACGCGCTGTCCCCCGCGTTTTAACCGCCAAGGGGATTACTCCCTAGTCTCCAGGCACGTGTCAGATATATACATCCCGAT",
          "organism": "Xenopus laevis",
          "uniprot_code": null,
          "uniprot_range_first": null,
          "uniprot_range_last": null,
          "oligomerization": "monomer",
          "molecular_type": "DNA",
          "uniprot_sequence": null,
          "mw": 92.093,
          "total_mw": 92.093,
          "number_molecules": 1,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
      ],
      "buffer": {
        "name": "20 mM Tris-Cl, 0.1 mM EDTA, 0.1 mM DTT, 50% sucrose, 1.9 M NaCl",
        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 7.5,
        "deuteration": null
      },
      "purity_method": null,
      "name": "Nucleosome Core Particle: 1.9 M NaCl, 50% sucrose, 50ms - 10s time resolved data",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": null,
            "address": "Ithaca, NY, United States",
            "full_name": "Cornell University",
            "webpage": "https://www.cornell.edu/"
          }
        ],
        "contributor_name": "Yujie",
        "contributor_surname": "Chen",
        "orcid": null
      }
    ],
    "concentration_method": null,
    "concentration_unit": null,
    "date": "2014-04-14",
    "storage_temperature": 0.0,
    "cell_temperature": 20.0,
    "exposure_time": 0.01,
    "number_of_frames": 5,
    "wavelength": 0.125,
    "sample_detector_distance": 2.5,
    "concentration_min": null,
    "concentration_max": 2.0,
    "sample_volume": null,
    "flow_rate": null,
    "s_min": 0.06,
    "s_max": 1.95,
    "total_exposure_time": null,
    "seccolumn": null
  },
  "fits": [],
  "estimated_volume_method": null,
  "pddf_software": null,
  "pddf_software_version": null,
  "i0_calibration_standard": null,
  "description": "From the depositor:\r\n\"Protein signal is blanked out in 50% sucrose, only DNA contributes to the scattering. \r\nHence, the SAXS profile reports the Rg and molecule weight of the DNA in the nucleosome core particle complex.\"",
  "experiment_description": "Synchrotron SAXS data from solutions of Nucleosome Core Particle in 20 mM Tris-Cl, 0.1 mM EDTA, 0.1 mM DTT, 50% sucrose, 1.9 M NaCl, pH 7.5 were collected on the 18ID beam line at the Advanced Photon Source (APS), Argonne National Laboratory (Lemont, IL, USA) using a Pilatus 100K detector at a sample-detector distance of 2.5 m and at a wavelength of λ = 0.125 nm (I(s) vs s, where s = 4π sin θ/λ and 2θ is the scattering angle). One solute concentration of 2.00 mg/ml was measured at 20°C through a time-course spanning 50 ms to 10 s (with a 50 ms delay time). The data displayed in this entry represent the scattering after 50 ms; the remaining data from the time series can be located in the full-entry zip archive.",
  "tags": [],
  "intensity_unit": null,
  "experimental_mw": 186.0,
  "experimental_mw_error": null,
  "guinier_i0_mw": 80.95,
  "guinier_i0_mw_error": 2.8,
  "porod_mw": null,
  "porod_mw_error": null,
  "pddf_i0": null,
  "pddf_i0_error": null,
  "guinier_i0": 146000.0,
  "guinier_i0_error": 10100.0,
  "pddf_rg": null,
  "pddf_rg_error": null,
  "guinier_rg": 6.78,
  "guinier_rg_error": 0.641,
  "pddf_dmax": null,
  "pddf_dmax_error": null,
  "porod_volume": null,
  "porod_volume_error": null,
  "estimated_volume": null,
  "estimated_volume_error": null,
  "guinier_point_first": 1,
  "guinier_point_last": 10,
  "pddf_point_first": null,
  "pddf_point_last": null,
  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDBT7_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2019-12-06T13:07:15.624532+01:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
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  "started_at": "2026-08-11T15:38:35.904912+00:00",
  "finished_at": "2026-08-11T15:38:41.370132+00:00",
  "source_last_modified": "2019-12-06T13:07:15.624532+01:00",
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