SASDEF2

Mitochondrial import inner membrane translocase complex TIM9·10

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
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Mitochondrial import inner membrane translocase complex TIM9·10

浓度1.0 – 5.0 缓冲液 / pH50mM Tris, 150mM NaCl / 7.4
实验温度20.0 设备 / 束线ESRF / BM29
波长0.099 nm曝光20.0 s × 1

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Mitochondrial import inner membrane translocase subunit TIM9
查看序列
MDALNSKEQQEFQKVVEQKQMKDFMRLYSNLVERCFTDCVNDFTTSKLTNKEQTCIMKCSEKFLKHSERVGQRFQEQNAALGQGLGR
proteinSaccharomyces cerevisiaeO74700—–—trimer分子数 310.202 kDa
Mitochondrial import inner membrane translocase subunit TIM10
查看序列
GSFLGFGGGQPQLSSQQKIQAAEAELDLVTDMFNKLVNNCYKKCINTSYSEGELNKNESSCLDRCVAKYFETNVQVGENMQKMGQSFNAAGKF
proteinSaccharomyces cerevisiaeP87108—–—trimer分子数 310.23 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
11038[3]0.05988624–4.938935 1/nm含误差列缺失 00sasbdb/entries/f2/sasdef2/source/SASDEF2.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)10.0—nm
i0Guinier49.970.03arbitrary
i0P(r)50.28—arbitrary
mwExperimental61.0—kDa
mwGuinier I(0)49.9710.0kDa
mwPorod61.0—kDa
porod_volumePorod103.0—nm³
rgGuinier2.670.01nm
rgP(r)2.725—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50mM Tris, 150mM NaCl缓冲液浓度—
pH7.4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2015-08-27储存 / 测量温度35.0 / 20.0
曝光时间20.0帧数1
波长0.099样品-探测器距离2.864
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线ESRF / BM29 · Grenoble, France
q 范围0.06 – 4.939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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pddfsasbdb/entries/f2/sasdef2/source/SASDEF2.outdownloaded6702285b235fb7b1c569ce957d36127fe174fb9906971b5d82363431995e4ecbd21dd下载查看原文件源站
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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:222 个字段值
字段路径原始值
codeSASDEF2
statusPublished
type_of_curveMerged
angular_unit1/nm
project.titleStructural Basis of Membrane Protein Chaperoning through the Mitochondrial Intermembrane Space.
project.publication.titleStructural Basis of Membrane Protein Chaperoning through the Mitochondrial Intermembrane Space.
project.publication.author_listWeinhäupl K, Lindau C, Hessel A, Wang Y, Schütze C, Jores T, Melchionda L, Schönfisch B, Kalbacher H, Bersch B, Rapaport D, Brennich M, Lindorff-Larsen K, Wiedemann N, Schanda P
project.publication.journalCell
project.publication.doi10.1016/j.cell.2018.10.039
project.publication.pmid30445040
project.publication.published_date2018 Nov 15
project.statusreleased
project.submitted_date2018-08-13
project.released_date2018-11-21
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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_nameMitochondrial import inner membrane translocase subunit TIM9
experiment.sample.molecule[0].short_nameTIM9
experiment.sample.molecule[0].sequenceMDALNSKEQQEFQKVVEQKQMKDFMRLYSNLVERCFTDCVNDFTTSKLTNKEQTCIMKCSEKFLKHSERVGQRFQEQNAALGQGLGR
experiment.sample.molecule[0].organismSaccharomyces cerevisiae
experiment.sample.molecule[0].uniprot_codeO74700
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationtrimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMDALNSKEQQEFQKVVEQKQMKDFMRLYSNLVERCFTDCVNDFTTSKLTNKEQTCIMKCS EKFLKHSERVGQRFQEQNAALGQGLGR
experiment.sample.molecule[0].mw10.202
experiment.sample.molecule[0].total_mw30.606
experiment.sample.molecule[0].number_molecules3
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_nameMitochondrial import inner membrane translocase subunit TIM10
experiment.sample.molecule[1].short_namenull
experiment.sample.molecule[1].sequenceGSFLGFGGGQPQLSSQQKIQAAEAELDLVTDMFNKLVNNCYKKCINTSYSEGELNKNESSCLDRCVAKYFETNVQVGENMQKMGQSFNAAGKF
experiment.sample.molecule[1].organismSaccharomyces cerevisiae
experiment.sample.molecule[1].uniprot_codeP87108
experiment.sample.molecule[1].uniprot_range_firstnull
experiment.sample.molecule[1].uniprot_range_lastnull
experiment.sample.molecule[1].oligomerizationtrimer
experiment.sample.molecule[1].molecular_typeprotein
experiment.sample.molecule[1].uniprot_sequenceMSFLGFGGGQPQLSSQQKIQAAEAELDLVTDMFNKLVNNCYKKCINTSYSEGELNKNESS CLDRCVAKYFETNVQVGENMQKMGQSFNAAGKF
experiment.sample.molecule[1].mw10.23
experiment.sample.molecule[1].total_mw30.69
experiment.sample.molecule[1].number_molecules3
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.buffer.name50mM Tris, 150mM 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.ph7.4
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameMitochondrial import inner membrane translocase complex TIM9·10
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
experiment.contributor[0].affiliation[0].addressGrenoble, France
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Grenoble Outstation
experiment.contributor[0].affiliation[0].webpagehttps://www.embl.fr/
experiment.contributor[0].contributor_nameMartha
experiment.contributor[0].contributor_surnameBrennich
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2015-08-27
experiment.storage_temperature35.0
experiment.cell_temperature20.0
experiment.exposure_time20.0
experiment.number_of_frames1
experiment.wavelength0.099
experiment.sample_detector_distance2.864
experiment.concentration_min1.0
experiment.concentration_max5.0
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.06
experiment.s_max4.939
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].chi_square_value1.86
fits[0].p_value0.0
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fits[1].chi_square_value1.378
fits[1].p_value0.0
fits[1].fit_residual_plotSASDEF2_fit2_fitresiduals_img.png
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fits[1].descriptionnull
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fits[2].models[0].type_of_modelatomic
fits[2].models[0].software_versionnull
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fits[2].models[0].symmetrynull
fits[2].models[0].commentThe model is a snapshot from the ensemble creating the fit.
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fits[2].softwareOther
fits[2].chi_square_value8.6175
fits[2].p_value0.0
fits[2].fit_residual_plotSASDEF2_fit3_fitresiduals_img.png
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fits[2].software_versionnull
fits[2].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of the mitochondrial import inner membrane translocase complex (TIM9·10) in 50mM Tris, 150mM NaCl, pH 7.4 were collected on the BM29 beam line at the ESRF (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). Solute concentrations ranging between 1 and 5 mg/ml were measured at 20°C. One 20 second frame was collected per concentration. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted. The low angle data collected at lower concentration were merged with the highest concentration high angle data to yield the final composite scattering curve.
tags[]
intensity_unitarbitrary
experimental_mw61.0
experimental_mw_errornull
guinier_i0_mw49.97
guinier_i0_mw_error10.0
porod_mw61.0
porod_mw_errornull
pddf_i050.28
pddf_i0_errornull
guinier_i049.97
guinier_i0_error0.03
pddf_rg2.725
pddf_rg_errornull
guinier_rg2.67
guinier_rg_error0.01
pddf_dmax10.0
pddf_dmax_errornull
porod_volume103.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first7
guinier_point_last91
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDEF2_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
codeSASDEF2
statussuccess
started_at2026-08-11T13:37:25.230308+00:00
finished_at2026-08-11T13:37:36.548963+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": "SASDEF2",
  "status": "Published",
  "type_of_curve": "Merged",
  "angular_unit": "1/nm",
  "project": {
    "title": "Structural Basis of Membrane Protein Chaperoning through the Mitochondrial Intermembrane Space.",
    "publication": {
      "title": "Structural Basis of Membrane Protein Chaperoning through the Mitochondrial Intermembrane Space.",
      "author_list": "Weinhäupl K, Lindau C, Hessel A, Wang Y, Schütze C, Jores T, Melchionda L, Schönfisch B, Kalbacher H, Bersch B, Rapaport D, Brennich M, Lindorff-Larsen K, Wiedemann N, Schanda P",
      "journal": "Cell",
      "doi": "10.1016/j.cell.2018.10.039",
      "pmid": "30445040",
      "published_date": "2018 Nov 15"
    },
    "status": "released",
    "submitted_date": "2018-08-13",
    "released_date": "2018-11-21"
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        "resolution": 172.0
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      "city": "Grenoble",
      "country": "France",
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      "beam_geometry": "",
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    },
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          "short_name": "TIM9",
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          "organism": "Saccharomyces cerevisiae",
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        },
        {
          "long_name": "Mitochondrial import inner membrane translocase subunit TIM10",
          "short_name": null,
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          "oligomerization": "trimer",
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        "concentration_unit": null,
        "comment": null,
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        "pka": null,
        "ph": 7.4,
        "deuteration": null
      },
      "purity_method": null,
      "name": "Mitochondrial import inner membrane translocase complex TIM9·10",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": "EMBL",
            "address": "Grenoble, France",
            "full_name": "European Molecular Biology Laboratory (EMBL) - Grenoble Outstation",
            "webpage": "https://www.embl.fr/"
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        ],
        "contributor_name": "Martha",
        "contributor_surname": "Brennich",
        "orcid": null
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    "concentration_method": null,
    "concentration_unit": null,
    "date": "2015-08-27",
    "storage_temperature": 35.0,
    "cell_temperature": 20.0,
    "exposure_time": 20.0,
    "number_of_frames": 1,
    "wavelength": 0.099,
    "sample_detector_distance": 2.864,
    "concentration_min": 1.0,
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    "total_exposure_time": null,
    "seccolumn": null
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      "software": "CORAL",
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      "p_value": 0.0,
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          "type_of_model": "dummy",
          "software_version": "r6669",
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          "symmetry": "C3",
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      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDEF2_fit2_fit_img.png",
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      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDEF2_fit3_fit_img.png",
      "software": "Other",
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  "experiment_description": "Synchrotron SAXS data from solutions of the mitochondrial import inner membrane translocase complex (TIM9·10) in 50mM Tris, 150mM NaCl, pH 7.4 were collected on the BM29 beam line at the ESRF (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). Solute concentrations ranging between 1 and 5 mg/ml were measured at 20°C. One 20 second frame was collected per concentration. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted. The low angle data collected at lower concentration were merged with the highest concentration high angle data to yield the final composite scattering curve.",
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  "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": "2026-08-11T13:37:25.230308+00:00",
  "finished_at": "2026-08-11T13:37:36.548963+00:00",
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