SASDEQ4

Deletion mutant of the suppressor of copper sensitivity C protein, PmScsC, with concentration series data

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2020-11-27T11:55:50.587847+01:00
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Deletion mutant of the suppressor of copper sensitivity C protein, PmScsC, with concentration series data

浓度— – 10.0 缓冲液 / pH10mM HEPES, 150mM NaCl / 7.4
实验温度10.0 设备 / 束线Australian Synchrotron / SAXS/WAXS
波长0.1033 nm曝光1.0 s × 38

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Deletion mutant of PmScsC
查看序列
SNAALNAAQEKEVRALVRDTLVSNPEILEEAIMALQTKALASEHDALYNDAASPRIGAKDAKLVLVSFTDYNCPYCKRFDPLLEKITEQYPDVAVIIKPLPFKGESSAKASQAVLSVWKEDPKAFLALHQRLMQKKTMLDNASIEDAMKSTNTSKIKLTDDSLKTLQNNLELSRKLGIQGTPATVIGDTILPGAVDYDQLEIIVKEQLAKVKK
proteinProteus mirabilisA0A1Z1SYD522–243unknown分子数 —23.438 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
1295[3]0.0159736425–0.3633577228 1/A含误差列缺失 00sasbdb/entries/q4/sasdeq4/source/SASDEQ4.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)9.05.0Å
i0Guinier0.24230.00011/cm
i0P(r)0.24130.00011/cm
mwExperimental44.3—kDa
porod_volumePorod54.0—ų
rgGuinier2.620.01Å
rgP(r)2.60.01Å

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

拟合 1 · Other 1

χ²:177.8886CorMap p:0.0单位:1/A

Fit from a linear combination of scattering profiles from monomeric, dimeric and trimeric PmScsCΔL

模型名称 / 类型软件对称性模型 MWPDB 声明来源文件
1—mixPDB (Protein Data Bank) P369.234XVW, 6MHH模型 图片
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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10mM HEPES, 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2018-04-05储存 / 测量温度4.0 / 10.0
曝光时间1.0帧数38
波长0.1033样品-探测器距离3.33
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线Australian Synchrotron / SAXS/WAXS · Melbourne, Australia
q 范围0.16 – 3.634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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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:163 个字段值
字段路径原始值
codeSASDEQ4
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleEngineered variants provide new insight into the structural properties important for activity of the highly dynamic, trimeric protein disulfide isomerase ScsC from Proteus mirabilis.
project.publication.titleEngineered variants provide new insight into the structural properties important for activity of the highly dynamic, trimeric protein disulfide isomerase ScsC from Proteus mirabilis.
project.publication.author_listFurlong EJ, Kurth F, Premkumar L, Whitten AE, Martin JL
project.publication.journalActa Crystallogr D Struct Biol
project.publication.doi10.1107/S2059798319000081
project.publication.pmid30950400
project.publication.published_date2019 Mar 1
project.statusreleased
project.submitted_date2018-09-18
project.released_date2019-03-29
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intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDEQ4.dat
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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_nameDeletion mutant of PmScsC
experiment.sample.molecule[0].short_namePmScsCΔL
experiment.sample.molecule[0].sequenceSNAALNAAQEKEVRALVRDTLVSNPEILEEAIMALQTKALASEHDALYNDAASPRIGAKDAKLVLVSFTDYNCPYCKRFDPLLEKITEQYPDVAVIIKPLPFKGESSAKASQAVLSVWKEDPKAFLALHQRLMQKKTMLDNASIEDAMKSTNTSKIKLTDDSLKTLQNNLELSRKLGIQGTPATVIGDTILPGAVDYDQLEIIVKEQLAKVKK
experiment.sample.molecule[0].organismProteus mirabilis
experiment.sample.molecule[0].uniprot_codeA0A1Z1SYD5
experiment.sample.molecule[0].uniprot_range_first22
experiment.sample.molecule[0].uniprot_range_last243
experiment.sample.molecule[0].oligomerizationunknown
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMKKTLSVLVISSLLFGANVQAAALNAAQEKEVRALVRDTLVSNPEILEEAIMALQTKKAD EQQAQFRQALASEHDALYNDAASPRIGAKDAKLVLVSFTDYNCPYCKRFDPLLEKITEQY PDVAVIIKPLPFKGESSAKASQAVLSVWKEDPKAFLALHQRLMQKKTMLDNASIEDAMKS TNTSKIKLTDDSLKTLQNNLELSRKLGIQGTPATVIGDTILPGAVDYDQLEIIVKEQLAK VKK
experiment.sample.molecule[0].mw23.438
experiment.sample.molecule[0].total_mw23.438
experiment.sample.molecule[0].number_molecules0
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.name10mM HEPES, 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.nameDeletion mutant of the suppressor of copper sensitivity C protein, PmScsC, with concentration series 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_nameANSTO
experiment.contributor[0].affiliation[0].addressKirrawee DC, NSW 2232, Australia
experiment.contributor[0].affiliation[0].full_nameAustralian Nuclear Science and Technology Organisation
experiment.contributor[0].affiliation[0].webpage
experiment.contributor[0].contributor_nameAndrew
experiment.contributor[0].contributor_surnameWhitten
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2018-04-05
experiment.storage_temperature4.0
experiment.cell_temperature10.0
experiment.exposure_time1.0
experiment.number_of_frames38
experiment.wavelength0.1033
experiment.sample_detector_distance3.33
experiment.concentration_minnull
experiment.concentration_max10.0
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.16
experiment.s_max3.634
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDEQ4_fit1_model1_img.png
fits[0].models[0].softwarePDB (Protein Data Bank)
fits[0].models[0].pdb_link[0].pdb_code4xvw
fits[0].models[0].pdb_link[0].ext_code4XVW
fits[0].models[0].pdb_link[0].ext_typepdb
fits[0].models[0].pdb_link[0].difference_with_modelidentical
fits[0].models[0].pdb_link[1].pdb_code6mhh
fits[0].models[0].pdb_link[1].ext_code6MHH
fits[0].models[0].pdb_link[1].ext_typepdb
fits[0].models[0].pdb_link[1].difference_with_modelidentical
fits[0].models[0].model_titlenull
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fits[0].models[0].software_versionnull
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fits[0].models[0].model_mw69.23
fits[0].models[0].bead_radiusnull
fits[0].models[0].lognull
fits[0].models[0].symmetryP3
fits[0].models[0].commentMonomer, dimer and trimer structures are all derived from this PDB (yet to be deposited)
fits[0].models[0].user111
fits[0].fit_unit1/A
fits[0].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/PmScsCDL_10p0_nZbPwQE_fit_img.png
fits[0].softwareOther
fits[0].chi_square_value177.8886
fits[0].p_value0.0
fits[0].fit_residual_plotPmScsCDL_10p0_nZbPwQE_fitresiduals_img.png
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fits[0].fit_lognull
fits[0].software_version1
fits[0].descriptionFit from a linear combination of scattering profiles from monomeric, dimeric and trimeric PmScsCΔL
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version4.6
i0_calibration_standardnull
descriptionnull
experiment_descriptionX-ray synchrotron radiation scattering data from solutions of a deletion mutant of Suppressor of Copper Sensitivity C protein (ScsC) protein from Proteus mirabilis in 10 mM HEPES 150mM NaCl, pH 7.4 were collected on the SAXS/WAXS beam line of the Australian Synchrotron (Melbourne, Australia) using a 2D Photon counting Pilatus 1M-W pixel detector (s = 4π sin θ/λ, where 2θ is the scattering angle). Thirty eight successive 1 second frames were collected across solute concentrations of 0.1-10.0 mg/ml at a sample temperature of 10°C. The data were normalized to the intensity of the transmitted beam and radially averaged and the scattering of the solvent-blank was subtracted. The SAXS data displayed this entry was derived from a 10.0 mg/ml sample and show that a mixture of monomer, dimer and trimer is present in solution. A linear combination of monomer, dimer and trimer are fit to the scattering curve, and the final concentration of each species in solution was determined to be: 122.70 µM (monomer); 73.15 µM (dimer); 12.29 µM (trimer). Together, with data collected at other concentration (available to download as a zip archive), it was estimated that K1 (monomer <-> dimer) was 205.81 µM, and K2 (monomer + dimer <-> trimer) 729.98 µM.
tags[]
intensity_unit1/cm
experimental_mw44.3
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i00.2413
pddf_i0_error0.0001
guinier_i00.2423
guinier_i0_error0.0001
pddf_rg2.6
pddf_rg_error0.01
guinier_rg2.62
guinier_rg_error0.01
pddf_dmax9.0
pddf_dmax_error5.0
porod_volume54.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last19
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDEQ4_datloglog_img.png
symmetrynull
last_modified2020-11-27T11:55:50.587847+01:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDEQ4
statussuccess
started_at2026-08-11T16:36:17.830638+00:00
finished_at2026-08-11T16:36:27.469103+00:00
source_last_modified2020-11-27T11:55:50.587847+01:00
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查看完整 summary.json 原文
{
  "code": "SASDEQ4",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Engineered variants provide new insight into the structural properties important for activity of the highly dynamic, trimeric protein disulfide isomerase ScsC from Proteus mirabilis.",
    "publication": {
      "title": "Engineered variants provide new insight into the structural properties important for activity of the highly dynamic, trimeric protein disulfide isomerase ScsC from Proteus mirabilis.",
      "author_list": "Furlong EJ, Kurth F, Premkumar L, Whitten AE, Martin JL",
      "journal": "Acta Crystallogr D Struct Biol",
      "doi": "10.1107/S2059798319000081",
      "pmid": "30950400",
      "published_date": "2019 Mar 1"
    },
    "status": "released",
    "submitted_date": "2018-09-18",
    "released_date": "2019-03-29"
  },
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      "beamline_name": "SAXS/WAXS",
      "beam_geometry": "Point",
      "type_of_source": "X-ray synchrotron",
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    "sample": {
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        {
          "long_name": "Deletion mutant of PmScsC",
          "short_name": "PmScsC&Delta;L",
          "sequence": "SNAALNAAQEKEVRALVRDTLVSNPEILEEAIMALQTKALASEHDALYNDAASPRIGAKDAKLVLVSFTDYNCPYCKRFDPLLEKITEQYPDVAVIIKPLPFKGESSAKASQAVLSVWKEDPKAFLALHQRLMQKKTMLDNASIEDAMKSTNTSKIKLTDDSLKTLQNNLELSRKLGIQGTPATVIGDTILPGAVDYDQLEIIVKEQLAKVKK",
          "organism": "Proteus mirabilis",
          "uniprot_code": "A0A1Z1SYD5",
          "uniprot_range_first": 22,
          "uniprot_range_last": 243,
          "oligomerization": "unknown",
          "molecular_type": "protein",
          "uniprot_sequence": "MKKTLSVLVISSLLFGANVQAAALNAAQEKEVRALVRDTLVSNPEILEEAIMALQTKKAD\nEQQAQFRQALASEHDALYNDAASPRIGAKDAKLVLVSFTDYNCPYCKRFDPLLEKITEQY\nPDVAVIIKPLPFKGESSAKASQAVLSVWKEDPKAFLALHQRLMQKKTMLDNASIEDAMKS\nTNTSKIKLTDDSLKTLQNNLELSRKLGIQGTPATVIGDTILPGAVDYDQLEIIVKEQLAK\nVKK",
          "mw": 23.438,
          "total_mw": 23.438,
          "number_molecules": 0,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
      ],
      "buffer": {
        "name": "10mM HEPES, 150mM NaCl",
        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 7.4,
        "deuteration": null
      },
      "purity_method": null,
      "name": "Deletion mutant of the suppressor of copper sensitivity C protein, PmScsC, with concentration series data",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": "ANSTO",
            "address": "Kirrawee DC, NSW 2232, Australia",
            "full_name": "Australian Nuclear Science and Technology Organisation",
            "webpage": ""
          }
        ],
        "contributor_name": "Andrew",
        "contributor_surname": "Whitten",
        "orcid": null
      }
    ],
    "concentration_method": null,
    "concentration_unit": null,
    "date": "2018-04-05",
    "storage_temperature": 4.0,
    "cell_temperature": 10.0,
    "exposure_time": 1.0,
    "number_of_frames": 38,
    "wavelength": 0.1033,
    "sample_detector_distance": 3.33,
    "concentration_min": null,
    "concentration_max": 10.0,
    "sample_volume": null,
    "flow_rate": null,
    "s_min": 0.16,
    "s_max": 3.634,
    "total_exposure_time": null,
    "seccolumn": null
  },
  "fits": [
    {
      "models": [
        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDEQ4_fit1_model1_img.png",
          "software": "PDB (Protein Data Bank)",
          "pdb_link": [
            {
              "pdb_code": "4xvw",
              "ext_code": "4XVW",
              "ext_type": "pdb",
              "difference_with_model": "identical"
            },
            {
              "pdb_code": "6mhh",
              "ext_code": "6MHH",
              "ext_type": "pdb",
              "difference_with_model": "identical"
            }
          ],
          "model_title": null,
          "type_of_model": "mix",
          "software_version": null,
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDEQ4_fit1_model1.pdb",
          "model_mw": 69.23,
          "bead_radius": null,
          "log": null,
          "symmetry": "P3",
          "comment": "Monomer, dimer and trimer structures are all derived from this PDB (yet to be deposited)",
          "user": 111
        }
      ],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/PmScsCDL_10p0_nZbPwQE_fit_img.png",
      "software": "Other",
      "chi_square_value": 177.8886,
      "p_value": 0.0,
      "fit_residual_plot": "PmScsCDL_10p0_nZbPwQE_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDEQ4_fit1.fit",
      "fit_log": null,
      "software_version": "1",
      "description": "Fit from a linear combination of scattering profiles from monomeric, dimeric and trimeric PmScsC&Delta;L"
    }
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  "estimated_volume_method": null,
  "pddf_software": "ATSAS GNOM",
  "pddf_software_version": "4.6",
  "i0_calibration_standard": null,
  "description": null,
  "experiment_description": "X-ray synchrotron radiation scattering data from solutions of a deletion mutant of Suppressor of Copper Sensitivity C protein (ScsC) protein from Proteus mirabilis in 10 mM HEPES 150mM NaCl, pH 7.4 were collected on the SAXS/WAXS beam line of the Australian Synchrotron (Melbourne, Australia) using a 2D Photon counting Pilatus 1M-W pixel detector (s = 4π sin θ/λ, where 2θ is the scattering angle). Thirty eight successive 1 second frames were collected across solute concentrations of 0.1-10.0 mg/ml at a sample temperature of 10°C. The data were normalized to the intensity of the transmitted beam and radially averaged and the scattering of the solvent-blank was subtracted. The SAXS data displayed this entry was derived from a 10.0 mg/ml sample and show that a mixture of monomer, dimer and trimer is present in solution. A linear combination of monomer, dimer and trimer are fit to the scattering curve, and the final concentration of each species in solution was determined to be: 122.70 µM (monomer); 73.15 µM (dimer); 12.29 µM (trimer). Together, with data collected at other concentration (available to download as a zip archive), it was estimated that K1 (monomer <-> dimer) was 205.81 µM, and K2 (monomer + dimer <-> trimer) 729.98 µM.",
  "tags": [],
  "intensity_unit": "1/cm",
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  "guinier_i0_mw": null,
  "guinier_i0_mw_error": null,
  "porod_mw": null,
  "porod_mw_error": null,
  "pddf_i0": 0.2413,
  "pddf_i0_error": 0.0001,
  "guinier_i0": 0.2423,
  "guinier_i0_error": 0.0001,
  "pddf_rg": 2.6,
  "pddf_rg_error": 0.01,
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  "guinier_rg_error": 0.01,
  "pddf_dmax": 9.0,
  "pddf_dmax_error": 5.0,
  "porod_volume": 54.0,
  "porod_volume_error": null,
  "estimated_volume": null,
  "estimated_volume_error": null,
  "guinier_point_first": 1,
  "guinier_point_last": 19,
  "pddf_point_first": null,
  "pddf_point_last": null,
  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDEQ4_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2020-11-27T11:55:50.587847+01:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
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  "started_at": "2026-08-11T16:36:17.830638+00:00",
  "finished_at": "2026-08-11T16:36:27.469103+00:00",
  "source_last_modified": "2020-11-27T11:55:50.587847+01:00",
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