SASDW97

Recombination directionality factor (6H-RdfS) from M.japonicum bound to 40mer DNA

数据类型:SASBDB 实验数据 状态:Published 曲线类型:SEC-SAS 最后更新:2025-04-02T23:34:23.155761+02:00
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Recombination directionality factor (6H-RdfS) from M.japonicum bound to 40mer DNA

浓度— – 6.8 缓冲液 / pH150 mM Tris-HCl, 300 mM NaCl, 5% v/v glycerol / 7.4
实验温度23.0 设备 / 束线Australian Synchrotron / SAXS/WAXS
波长0.10332 nm曝光1.0 s × 800

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Recombination directionality factor RdfS
查看序列
MKHHHHHHPMSDYDIPTTENLYFQGAMDDENDRAARAKKGSPFLNTAQAAFYIGLSQRTLEKMRLTGGGPKYRKHGRYVRYHIDELDDWSKGRPPEPGSDDDKGGSGSADEGARS
proteinMesorhizobium japonicum R7AQ7AL96—–—tetramer分子数 412.941 kDa
attP_8 40-mer DNA
查看序列
GAATTTCGGCGCAGTTGGTCCAACGAGGCGGGGGGCTGGT
DNA———–—dimer分子数 212.57 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
1670[3]0.003681128–0.3819378 1/A含误差列缺失 0100sasbdb/entries/97/sasdw97/source/SASDW97.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)13.8—Å
i0Guinier0.0853579—1/cm
i0P(r)0.08632—1/cm
mwExperimental83.0—kDa
mwPorod88.0—kDa
porod_volumePorod134.0—ų
rgGuinier3.80.07Å
rgP(r)3.8280.07Å

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150 mM Tris-HCl, 300 mM NaCl, 5% v/v glycerol缓冲液浓度—
pH7.4添加剂—
缓冲液说明SAXS buffer, identical to SASDPK4
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2019-06-19储存 / 测量温度23.0 / 23.0
曝光时间1.0帧数800
波长0.10332样品-探测器距离1.6
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线Australian Synchrotron / SAXS/WAXS · Melbourne, Australia
q 范围0.037 – 3.819样品体积 / 流速50.0 / 0.3

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
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full_entry_zipsasbdb/entries/97/sasdw97/source/SASDW97.zipdownloaded233851b75d1e13197d61bfd8fcc30e9fe8ef0258b4cc619514edb5394531fd206c4227下载查看原文件源站
pddfsasbdb/entries/97/sasdw97/source/SASDW97.outdownloaded36646b03a033a9dc0d09cde83d077cba9d931e27af6791f0dcc773d0295246d5541c6下载查看原文件源站
sascifsasbdb/entries/97/sasdw97/source/SASDW97.sascifnot_available——下载查看原文件源站
summarysasbdb/entries/97/sasdw97/source/summary.jsondownloaded970293e774b26bef6acff2decc1a18e8f2624ca0e4f8758314427e01386bfa28a1c5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(6 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:196 个字段值
字段路径原始值
codeSASDW97
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleStructural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS
project.publication.titleStructural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS
project.publication.author_listVerdonk C, Agostino M, Eto K, Hall D, Bond C, Ramsay J
project.publication.journalNucleic Acids Research
project.publication.doi10.1093/nar/gkaf249
project.publication.pmidnull
project.publication.published_date2025 Apr 02
project.statusreleased
project.submitted_date2025-02-11
project.released_date2025-03-29
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experiment.instrument.detector.typeDectris
experiment.instrument.detector.namePilatus 1M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameAustralian Synchrotron
experiment.instrument.cityMelbourne
experiment.instrument.countryAustralia
experiment.instrument.beamline_nameSAXS/WAXS
experiment.instrument.beam_geometryPoint
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourceTrue
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_nameRecombination directionality factor RdfS
experiment.sample.molecule[0].short_nameRdfS
experiment.sample.molecule[0].sequenceMKHHHHHHPMSDYDIPTTENLYFQGAMDDENDRAARAKKGSPFLNTAQAAFYIGLSQRTLEKMRLTGGGPKYRKHGRYVRYHIDELDDWSKGRPPEPGSDDDKGGSGSADEGARS
experiment.sample.molecule[0].organismMesorhizobium japonicum R7A
experiment.sample.molecule[0].uniprot_codeQ7AL96
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationtetramer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMDDENDRAARAKKGSPFLNTAQAAFYIGLSQRTLEKMRLTGGGPKYRKHGRYVRYHIDEL DDWSKGRPPEPGSDDDKGGSGSADEGARS
experiment.sample.molecule[0].mw12.941
experiment.sample.molecule[0].total_mw51.764
experiment.sample.molecule[0].number_molecules4
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionN-terminal Hexahistidine-tagged RdfS protein
experiment.sample.molecule[1].long_nameattP_8 40-mer DNA
experiment.sample.molecule[1].short_nameattP_8
experiment.sample.molecule[1].sequenceGAATTTCGGCGCAGTTGGTCCAACGAGGCGGGGGGCTGGT
experiment.sample.molecule[1].organismnull
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_typeDNA
experiment.sample.molecule[1].uniprot_sequence
experiment.sample.molecule[1].mw12.57
experiment.sample.molecule[1].total_mw25.14
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_descriptiondsDNA 40mer oligomer synthetic DNA
experiment.sample.buffer.name150 mM Tris-HCl, 300 mM NaCl, 5% v/v glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentSAXS buffer, identical to SASDPK4
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.4
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameRecombination directionality factor (6H-RdfS) from M.japonicum bound to 40mer DNA
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].addressnull
experiment.contributor[0].affiliation[0].full_nameCurtin University
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameJoshua
experiment.contributor[0].contributor_surnameRamsay
experiment.contributor[0].orcidhttps://orcid.org/0000-0002-1301-7077
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2019-06-19
experiment.storage_temperature23.0
experiment.cell_temperature23.0
experiment.exposure_time1.0
experiment.number_of_frames800
experiment.wavelength0.10332
experiment.sample_detector_distance1.6
experiment.concentration_minnull
experiment.concentration_max6.8
experiment.sample_volume50.0
experiment.flow_rate0.3
experiment.s_min0.037
experiment.s_max3.819
experiment.total_exposure_timenull
experiment.seccolumn2
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fits[0].chi_square_value21.753
fits[0].p_value0.0
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fits[1].softwareDAMMIF
fits[1].chi_square_value0.302
fits[1].p_value0.0104
fits[1].fit_residual_plotSASDW97_fit2_fitresiduals_img.png
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fits[1].software_version3.1.3
fits[1].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of His-tagged RdfS excisionase bound to dsDNA 40mer attP_8 in 150 mM Tris-HCl, 300 mM NaCl, 5% v/v glycerol, pH 7.4 were collected on the SAXS/WAXS beam line at the Australian Synchrotron (Melbourne, Australia) using a Pilatus 1M detector at a sample-detector distance of 2.6 m and at a wavelength of λ = 0.103 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 50.00 μl samples at 6H-RdfS at 390 µM, dsDNA attP_8 at 500 µM was injected at a 0.30 ml/min flow rate onto a GE Superdex 200 Increase 5/150 column at 23°C. 36 successive 1 second data frames were selected from the SEC sample peak (from a total of 800 individual frames measured from the entire SEC elution) and processed to generate the profile displayed in this entry. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[]
intensity_unit1/cm
experimental_mw83.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw88.0
porod_mw_errornull
pddf_i00.08632
pddf_i0_errornull
guinier_i00.0853579
guinier_i0_errornull
pddf_rg3.828
pddf_rg_error0.07
guinier_rg3.8
guinier_rg_error0.07
pddf_dmax13.8
pddf_dmax_errornull
porod_volume134.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first30
guinier_point_last51
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDW97_datloglog_img.png
symmetrynull
last_modified2025-04-02T23:34:23.155761+02:00
bragg_peak[]
manifest.json:34 个字段值
字段路径原始值
codeSASDW97
statussuccess
started_at2026-08-11T15:24:59.569451+00:00
finished_at2026-08-11T15:25:09.584142+00:00
source_last_modified2025-04-02T23:34:23.155761+02:00
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查看完整 summary.json 原文
{
  "code": "SASDW97",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "Structural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS",
    "publication": {
      "title": "Structural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS",
      "author_list": "Verdonk C, Agostino M, Eto K, Hall D, Bond C, Ramsay J",
      "journal": "Nucleic Acids Research",
      "doi": "10.1093/nar/gkaf249",
      "pmid": null,
      "published_date": "2025 Apr 02"
    },
    "status": "released",
    "submitted_date": "2025-02-11",
    "released_date": "2025-03-29"
  },
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        "name": "Pilatus 1M",
        "resolution": 172.0
      },
      "name": "Australian  Synchrotron",
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      "country": "Australia",
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      "sample_path_length": null,
      "line_collimation_slitlength": null,
      "line_collimation_integrationwidth": null,
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          "oligomerization": "dimer",
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        "concentration_unit": null,
        "comment": "SAXS buffer, identical to SASDPK4",
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        "concentration": null,
        "pka": null,
        "ph": 7.4,
        "deuteration": null
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      "purity_method": null,
      "name": "Recombination directionality factor (6H-RdfS) from M.japonicum bound to 40mer DNA",
      "ext_coefficient": null,
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      "absorbption": null,
      "deuteration": null,
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    "contributor": [
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        "affiliation": [
          {
            "short_name": null,
            "address": null,
            "full_name": "Curtin University",
            "webpage": null
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        ],
        "contributor_name": "Joshua",
        "contributor_surname": "Ramsay",
        "orcid": "https://orcid.org/0000-0002-1301-7077"
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    "concentration_method": null,
    "concentration_unit": null,
    "date": "2019-06-19",
    "storage_temperature": 23.0,
    "cell_temperature": 23.0,
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    "wavelength": 0.10332,
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    "concentration_max": 6.8,
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      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDW97_fit1_fixed_fit_img.png",
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      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDW97_fit1.fit",
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  "last_modified": "2025-04-02T23:34:23.155761+02:00",
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}
查看完整 manifest.json 原文
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