SASDEE9

TraI_2_C domain of TraI

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

Please note: The protein contains unstructured regions that impart a level of flexibility to the overall structure in solution. As a consequence, the conformational state(s) sampled by the protein differs from - and cannot be captured by - the single predicted PHYRE2 atomistic model/representation displayed in this entry (as evidenced by the poor fit of the model to the SAXS data; bottom).

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · TraI_2_C domain of TraI

浓度1.0 – 4.57 缓冲液 / pH50 mM TRIS-HCl 100 mM NaCl / 8.0
实验温度4.0 设备 / 束线ESRF / BM29
波长0.099 nm曝光1.0 s × 10

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
TraI_2_C domain of TraI
查看序列
MSASGVKNMAELEAIVSERNLKKQSETESTEIVEDSVKAKHMEARDRGMQFLRWLADGLGDGSIAVNRSGATVHFIEQGMLLVTPAVFRDYAGGVFNKSDTESLGPLTQKGFEALRLHARTKKSSLHRVLTTNGSNRRLFYCYLIPEHNIKHIIQPGSRPQNNTDIKLDESDLLVMEQKALEVLFQ
proteinNeisseria gonorrhoeaeQ5EPC7674–850monomer分子数 120.813 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
1924[3]0.0585562–4.42077 1/nm含误差列缺失 00sasbdb/entries/e9/sasdee9/source/SASDEE9.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)6.46—nm
i0Guinier17.940.03—
i0P(r)17.57——
mwExperimental20.38—kDa
mwGuinier I(0)17.76—kDa
mwPorod25.41—kDa
porod_volumePorod40.06—nm³
rgGuinier2.230.04nm
rgP(r)2.183—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50 mM TRIS-HCl 100 mM NaCl缓冲液浓度—
pH8.0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2018-07-11储存 / 测量温度4.0 / 4.0
曝光时间1.0帧数10
波长0.099样品-探测器距离2.867
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线ESRF / BM29 · Grenoble, France
q 范围0.059 – 4.421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
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curve:来源记录
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pddf:来源记录
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sascif: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
codeSASDEE9
statusPublished
type_of_curveMerged
angular_unit1/nm
project.titleDNA processing by the MOBH family relaxase TraI encoded within the gonococcal genetic island.
project.publication.titleDNA processing by the MOBH family relaxase TraI encoded within the gonococcal genetic island.
project.publication.author_listHeilers JH, Reiners J, Heller EM, Golzer A, Smits SHJ, van der Does C
project.publication.journalNucleic Acids Res
project.publication.doi10.1093/nar/gkz577
project.publication.pmid31276596
project.publication.published_date2019 Sep 5
project.statusreleased
project.submitted_date2018-12-22
project.released_date2019-07-09
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experiment.instrument.detector.typeDectris
experiment.instrument.detector.namePilatus 1M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameESRF
experiment.instrument.cityGrenoble
experiment.instrument.countryFrance
experiment.instrument.beamline_nameBM29
experiment.instrument.beam_geometry
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_nameTraI_2_C domain of TraI
experiment.sample.molecule[0].short_nameTraI_2_C
experiment.sample.molecule[0].sequenceMSASGVKNMAELEAIVSERNLKKQSETESTEIVEDSVKAKHMEARDRGMQFLRWLADGLG DGSIAVNRSGATVHFIEQGMLLVTPAVFRDYAGGVFNKSDTESLGPLTQKGFEALRLHAR TKKSSLHRVLTTNGSNRRLFYCYLIPEHNIKHIIQPGSRPQNNTDIKLDESDLLVMEQKA LEVLFQ
experiment.sample.molecule[0].organismNeisseria gonorrhoeae
experiment.sample.molecule[0].uniprot_codeQ5EPC7
experiment.sample.molecule[0].uniprot_range_first674
experiment.sample.molecule[0].uniprot_range_last850
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMKTSLLTIASSLMLVSGSMLYLINTRKSTDSVSHNDEVAHINQNIVNDRFRILNAHELIQ VLDLSPQISGIKMNLGLSDENWSKDALPFLEKYIAFVQRLPASESHHHAGDGGLVRHTLD VAALALVASTSQSWPPNAKTEEIAKKTAVWRYGIMCAALLHDVGKTVTGFQVELFDSAIS LEKLLWLPDTGSMAESGKLYYRVEFPDAKSAYSTHAEIAWTFFQALVPSHVRQWLATTDP NLMITLRNYLSGKKDGSPLEQLIKNADMTSVSRDLRSGSRQRFSTAKRKPFIETIMETLK EMLSDRGVHFSIATTAGGDLFRKGDRIYLMSKNVPDYIRQYLRKNQHPAAGSFPADNQRI FDTLFEYRAVIPPENDPHRAINHIEVEFTRMDGEKVRNIFSVLCFNAKTLYPDGDYPTEF LGNLSEVSAKKEIPDVVVSEDKVSTQIQGAEDNPVTMTKDKMDFLSIQPVTAEQPPLPEK NQTETANSAFDNSMNTAAPAENKSSESEKAKEPGYGTIDNLIENFNLIEADSEQTESTKS EAETAENAVNLVQENIRVEVKTETVDKPRAEVKETETDKAPKTIKSGTKASRKKLAGLFA DNRKPIGKTAEPDAQIKTTETVTHQIDSEAVSLPESESAQNGMRELERLRLREPTSSPRP VQVMDDSEGLDSLASGVKNMAELEAIVSERNLKKQSETESTEIVEDSVKAKHMEARDRGM QFLRWLADGLGDGSIAVNRSGATVHFIEQGMLLVTPAVFRDYAGGVFNKSDTESLGPLTQ KGFEALRLHARTKKSSLHRVLTTNGSNRRLFYCYLIPEHNIQHIIQPGSRPQNNTDIKLD ESDLLVMEQK
experiment.sample.molecule[0].mw20.813
experiment.sample.molecule[0].total_mw20.813
experiment.sample.molecule[0].number_molecules1
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.name50 mM TRIS-HCl 100 mM 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.ph8.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameTraI_2_C domain of TraI
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].addressDüsseldorf, Germany
experiment.contributor[0].affiliation[0].full_nameHeinrich Heine University Düsseldorf
experiment.contributor[0].affiliation[0].webpagehttps://www.uni-duesseldorf.de
experiment.contributor[0].contributor_nameJens
experiment.contributor[0].contributor_surnameReiners
experiment.contributor[0].orcid
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2018-07-11
experiment.storage_temperature4.0
experiment.cell_temperature4.0
experiment.exposure_time1.0
experiment.number_of_frames10
experiment.wavelength0.099
experiment.sample_detector_distance2.867
experiment.concentration_min1.0
experiment.concentration_max4.57
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.059
experiment.s_max4.421
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[1].chi_square_value4.165
fits[1].p_value0.0
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fits[1].software_versionnull
fits[1].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionPlease note: The protein contains unstructured regions that impart a level of flexibility to the overall structure in solution. As a consequence, the conformational state(s) sampled by the protein differs from - and cannot be captured by - the single predicted PHYRE2 atomistic model/representation displayed in this entry (as evidenced by the poor fit of the model to the SAXS data; bottom).
experiment_descriptionSynchrotron SAXS data from solutions of the TraI_2_C domain of TraI in 50 mM TRIS-HCl, pH 8, 100 mM NaCl, were collected on the BM29 beam line at the ESRF storage ring (Grenoble, France) using a Pilatus 1M detector at a sample-detector distance of 2.9 m and at a wavelength of λ = 0.099 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Possible aggregates were removed using a Superdex 200 10/300 (GE Healthcare) size-exclusion chromatography (SEC) column pre-equilibrated with buffer at a flow rate of 0.5 mL/min at the EMBL-Lab outstation (Grenoble). All measurements were performed at 4°C. The sample concentration range was 1 to 4.6 mg/mL. For online-SEC one frame was collected every two seconds and for static measurements ten frames of data were collected with total exposure time of one second. By comparison of these frames, the possibility of radiation damage during the measurement was excluded. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted. All used programs for data processing were part of the ATSAS Software package (Version 2.8.4).
tags[]
intensity_unitnull
experimental_mw20.38
experimental_mw_errornull
guinier_i0_mw17.76
guinier_i0_mw_errornull
porod_mw25.41
porod_mw_errornull
pddf_i017.57
pddf_i0_errornull
guinier_i017.94
guinier_i0_error0.03
pddf_rg2.183
pddf_rg_errornull
guinier_rg2.23
guinier_rg_error0.04
pddf_dmax6.46
pddf_dmax_errornull
porod_volume40.06
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first47
guinier_point_last111
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDEE9_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDEE9
statussuccess
started_at2026-08-11T16:12:49.045005+00:00
finished_at2026-08-11T16:12:58.929913+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": "SASDEE9",
  "status": "Published",
  "type_of_curve": "Merged",
  "angular_unit": "1/nm",
  "project": {
    "title": "DNA processing by the MOBH family relaxase TraI encoded within the gonococcal genetic island.",
    "publication": {
      "title": "DNA processing by the MOBH family relaxase TraI encoded within the gonococcal genetic island.",
      "author_list": "Heilers JH, Reiners J, Heller EM, Golzer A, Smits SHJ, van der Does C",
      "journal": "Nucleic Acids Res",
      "doi": "10.1093/nar/gkz577",
      "pmid": "31276596",
      "published_date": "2019 Sep 5"
    },
    "status": "released",
    "submitted_date": "2018-12-22",
    "released_date": "2019-07-09"
  },
  "pddf_data": "https://www.sasbdb.org/media/p_of_R_files/SASDEE9.out",
  "intensities_data": "https://www.sasbdb.org/media/intensities_files/SASDEE9.dat",
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  "experiment": {
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      "country": "France",
      "beamline_name": "BM29",
      "beam_geometry": "",
      "type_of_source": "X-ray synchrotron",
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    },
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          "short_name": "TraI_2_C",
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          "organism": "Neisseria gonorrhoeae",
          "uniprot_code": "Q5EPC7",
          "uniprot_range_first": 674,
          "uniprot_range_last": 850,
          "oligomerization": "monomer",
          "molecular_type": "protein",
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        "deuteration": null
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      "name": "TraI_2_C domain of TraI",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
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      "absorbption": null,
      "deuteration": null,
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    "contributor": [
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        "affiliation": [
          {
            "short_name": null,
            "address": "Düsseldorf, Germany",
            "full_name": "Heinrich Heine University Düsseldorf",
            "webpage": "https://www.uni-duesseldorf.de"
          }
        ],
        "contributor_name": "Jens",
        "contributor_surname": "Reiners",
        "orcid": ""
      }
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    "concentration_unit": null,
    "date": "2018-07-11",
    "storage_temperature": 4.0,
    "cell_temperature": 4.0,
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    "wavelength": 0.099,
    "sample_detector_distance": 2.867,
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          "software": "GASBOR",
          "pdb_link": [],
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          "type_of_model": "dummy",
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      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/DuffstA_5FHaBX9_fit_img.png",
      "software": "GASBOR",
      "chi_square_value": 0.8,
      "p_value": 0.0,
      "fit_residual_plot": "DuffstA_5FHaBX9_fitresiduals_img.png",
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      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/DuffModel00_WDBHIMq_fit_img.png",
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  "description": "Please note: The protein contains unstructured regions that impart a level of flexibility to the overall structure in solution. As a consequence, the conformational state(s) sampled by the protein differs from - and cannot be captured by - the single predicted PHYRE2 atomistic model/representation displayed in this entry (as evidenced by the poor fit of the model to the SAXS data; bottom).",
  "experiment_description": "Synchrotron SAXS data from solutions of the TraI_2_C domain of TraI in 50 mM TRIS-HCl, pH 8, 100 mM NaCl, were collected on the BM29 beam line at the ESRF storage ring (Grenoble, France) using a Pilatus 1M detector at a sample-detector distance of 2.9 m and at a wavelength of λ = 0.099 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Possible aggregates were removed using a Superdex 200 10/300 (GE Healthcare) size-exclusion chromatography (SEC) column pre-equilibrated with buffer at a flow rate of 0.5 mL/min at the EMBL-Lab outstation (Grenoble). All measurements were performed at 4°C. The sample concentration range was 1 to 4.6 mg/mL. For online-SEC one frame was collected every two seconds and for static measurements ten frames of data were collected with total exposure time of one second.  By comparison of these frames, the possibility of radiation damage during the measurement was excluded. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted. All used programs for data processing were part of the ATSAS Software package (Version 2.8.4).",
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  "guinier_point_first": 47,
  "guinier_point_last": 111,
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  "intensities_log_log_plot": "SASDEE9_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": "2026-08-11T16:12:49.045005+00:00",
  "finished_at": "2026-08-11T16:12:58.929913+00:00",
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