SASDEC2

Cell wall synthesis protein Wag31: Polymer tbWag31 T73A

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2020-08-13T15:33:49.909979+02:00

The cell wall synthesis protein Wag31: Polymer tbWag31 T73A forms a large super-macromolecular assembly (supported by atomic force microscopy, AFM) and as a result there is a very limited angular range to estimate the radius of gyration, Rg, using the Guinier approximation. In addition, the quoted monomer molecular weight does not apply to this sample. The probable distribution of real-space scattering pair vector lengths (p(r) vs r profile or PDDF) represents the cross-sectional pair distribution function for rod-like particle (option 4 in GNOM) and the subsequent data validation tools for this entry are based on the corresponding cross section parameters (Rg of cross section and Dmax of cross section). The I(s) is recorded in a relative scale in kDa units assuming a 1 mg/ml sample concentration. However the experimental concentration was found to be 2.7 mg/ml (assessed using a Bradford assay).

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Cell wall synthesis protein Wag31: Polymer tbWag31 T73A

浓度— – 2.7 缓冲液 / pH50mM Tris pH7.5, 300mM NaCl, 10% Glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME) / 7.5
实验温度4.0 设备 / 束线ESRF / BM29
波长0.1 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
Cell wall synthesis protein Wag31
查看序列
MHHHHHHENLYFQGPLTPADVHNVAFSKPPIGKRGYNEDEVDAFLDLVENELTRLIEENSDLRQRINELDQELAAGGGAGVTPQAAQAIPAYEPEPGKPAPAAVSAGMNEEQALKAARVLSLAQDTADRLTNTAKAESDKMLADARANAEQILGEARHTADATVAEARQRADAMLADAQSRSEAQLRQAQEKADALQADAERKHSEIMGTINQQRAVLEGRLEQLRTFEREYRTRLKTYLESQLEELGQRGSAAPVDSNADAGGFDQFNRGKN
proteinMycobacterium tuberculosisP9WMU1—–—unknown分子数 —29.922 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
11043[3]0.03850123–4.933519 1/nm含误差列缺失 092sasbdb/entries/c2/sasdec2/source/SASDEC2.dat
▼

2. SASBDB 报告的指标 Reported Results

指标方法数值误差单位
dmaxP(r)13.55—nm
i0Guinier990.3317.9arbitrary
i0P(r)34.660.08arbitrary
mwExperimental29.9—kDa
rgGuinier21.80.409nm
rgP(r)3.320.021nm

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

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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 pH7.5, 300mM NaCl, 10% Glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME)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2017-12-15储存 / 测量温度4.0 / 4.0
曝光时间1.0帧数10
波长0.1样品-探测器距离2.87
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线ESRF / BM29 · Grenoble, France
q 范围0.039 – 4.934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/c2/sasdec2/source/SASDEC2.outdownloaded328289d85cb2a8ca4b185c24afc7240556bce2dee471874b6be2df7434fee1c8c51f3下载查看原文件源站
sascifsasbdb/entries/c2/sasdec2/source/SASDEC2.sascifdownloaded876432172d7df9af94aeab266b4294510e220c506d0723b9fc8c8deb76463ece0fc83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(2 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:134 个字段值
字段路径原始值
codeSASDEC2
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleHigher order assembling of the mycobacterial polar growth factor DivIVA/Wag31.
project.publication.titleHigher order assembling of the mycobacterial polar growth factor DivIVA/Wag31.
project.publication.author_listChoukate K, Gupta A, Basu B, Virk K, Ganguli M, Chaudhuri B
project.publication.journalJ Struct Biol
project.publication.doi10.1016/j.jsb.2019.107429
project.publication.pmid31778770
project.publication.published_date2019 Nov 25
project.statusreleased
project.submitted_date2019-01-30
project.released_date2020-01-09
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDEC2.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDEC2.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEC2_dat_img.png
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intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEC2_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDEC2.sascif
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_nameCell wall synthesis protein Wag31
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceMHHHHHHENLYFQGPLTPADVHNVAFSKPPIGKRGYNEDEVDAFLDLVENELTRLIEENSDLRQRINELDQEL AAGGGAGVTPQAAQAIPAYEPEPGKPAPAAVSAGMNEEQALKAARVLSLAQDTADRLTNT AKAESDKMLADARANAEQILGEARHTADATVAEARQRADAMLADAQSRSEAQLRQAQEKA DALQADAERKHSEIMGTINQQRAVLEGRLEQLRTFEREYRTRLKTYLESQLEELGQRGSA APVDSNADAGGFDQFNRGKN
experiment.sample.molecule[0].organismMycobacterium tuberculosis
experiment.sample.molecule[0].uniprot_codeP9WMU1
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationunknown
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMPLTPADVHNVAFSKPPIGKRGYNEDEVDAFLDLVENELTRLIEENSDLRQRINELDQEL AAGGGAGVTPQATQAIPAYEPEPGKPAPAAVSAGMNEEQALKAARVLSLAQDTADRLTNT AKAESDKMLADARANAEQILGEARHTADATVAEARQRADAMLADAQSRSEAQLRQAQEKA DALQADAERKHSEIMGTINQQRAVLEGRLEQLRTFEREYRTRLKTYLESQLEELGQRGSA APVDSNADAGGFDQFNRGKN
experiment.sample.molecule[0].mw29.922
experiment.sample.molecule[0].total_mw29.922
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.name50mM Tris pH7.5, 300mM NaCl, 10% Glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME)
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.nameCell wall synthesis protein Wag31: Polymer tbWag31 T73A
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_nameCSIR
experiment.contributor[0].affiliation[0].addressChandigarh, India
experiment.contributor[0].affiliation[0].full_nameCSIR-Institute of Microbial Technology
experiment.contributor[0].affiliation[0].webpagehttp://www.imtech.res.in/
experiment.contributor[0].contributor_nameKomal
experiment.contributor[0].contributor_surnameChoukate
experiment.contributor[0].orcid
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2017-12-15
experiment.storage_temperature4.0
experiment.cell_temperature4.0
experiment.exposure_time1.0
experiment.number_of_frames10
experiment.wavelength0.1
experiment.sample_detector_distance2.87
experiment.concentration_minnull
experiment.concentration_max2.7
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.039
experiment.s_max4.934
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[]
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version4.6
i0_calibration_standardnull
descriptionThe cell wall synthesis protein Wag31: Polymer tbWag31 T73A forms a large super-macromolecular assembly (supported by atomic force microscopy, AFM) and as a result there is a very limited angular range to estimate the radius of gyration, Rg, using the Guinier approximation. In addition, the quoted monomer molecular weight does not apply to this sample. The probable distribution of real-space scattering pair vector lengths (p(r) vs r profile or PDDF) represents the cross-sectional pair distribution function for rod-like particle (option 4 in GNOM) and the subsequent data validation tools for this entry are based on the corresponding cross section parameters (Rg of cross section and Dmax of cross section). The I(s) is recorded in a relative scale in kDa units assuming a 1 mg/ml sample concentration. However the experimental concentration was found to be 2.7 mg/ml (assessed using a Bradford assay).
experiment_descriptionSynchrotron SAXS data from solutions of the polymeric form of Wag31 T73A in 50mM Tris, 300mM NaCl, 10% glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME), pH 7.5 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 = 0.1 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 2.70 mg/ml was measured at 4°C. 10 successive 1 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[]
intensity_unitarbitrary
experimental_mw29.9
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i034.66
pddf_i0_error0.08
guinier_i0990.33
guinier_i0_error17.9
pddf_rg3.32
pddf_rg_error0.021
guinier_rg21.8
guinier_rg_error0.409
pddf_dmax13.55
pddf_dmax_errornull
porod_volumenull
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last6
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDEC2_datloglog_img.png
symmetrynull
last_modified2020-08-13T15:33:49.909979+02:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDEC2
statussuccess
started_at2026-08-11T13:35:18.421460+00:00
finished_at2026-08-11T13:35:27.780993+00:00
source_last_modified2020-08-13T15:33:49.909979+02:00
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查看完整 summary.json 原文
{
  "code": "SASDEC2",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
  "project": {
    "title": "Higher order assembling of the mycobacterial polar growth factor DivIVA/Wag31.",
    "publication": {
      "title": "Higher order assembling of the mycobacterial polar growth factor DivIVA/Wag31.",
      "author_list": "Choukate K, Gupta A, Basu B, Virk K, Ganguli M, Chaudhuri B",
      "journal": "J Struct Biol",
      "doi": "10.1016/j.jsb.2019.107429",
      "pmid": "31778770",
      "published_date": "2019 Nov 25"
    },
    "status": "released",
    "submitted_date": "2019-01-30",
    "released_date": "2020-01-09"
  },
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  "intensities_data": "https://www.sasbdb.org/media/intensities_files/SASDEC2.dat",
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      },
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      "country": "France",
      "beamline_name": "BM29",
      "beam_geometry": "",
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    "sample": {
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        {
          "long_name": "Cell wall synthesis protein Wag31",
          "short_name": null,
          "sequence": "MHHHHHHENLYFQGPLTPADVHNVAFSKPPIGKRGYNEDEVDAFLDLVENELTRLIEENSDLRQRINELDQEL\r\nAAGGGAGVTPQAAQAIPAYEPEPGKPAPAAVSAGMNEEQALKAARVLSLAQDTADRLTNT\r\nAKAESDKMLADARANAEQILGEARHTADATVAEARQRADAMLADAQSRSEAQLRQAQEKA\r\nDALQADAERKHSEIMGTINQQRAVLEGRLEQLRTFEREYRTRLKTYLESQLEELGQRGSA\r\nAPVDSNADAGGFDQFNRGKN",
          "organism": "Mycobacterium tuberculosis",
          "uniprot_code": "P9WMU1",
          "uniprot_range_first": null,
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          "oligomerization": "unknown",
          "molecular_type": "protein",
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          "mw": 29.922,
          "total_mw": 29.922,
          "number_molecules": 0,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
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        "pka": null,
        "ph": 7.5,
        "deuteration": null
      },
      "purity_method": null,
      "name": "Cell wall synthesis protein Wag31: Polymer tbWag31 T73A",
      "ext_coefficient": null,
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    },
    "contributor": [
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          {
            "short_name": "CSIR",
            "address": "Chandigarh, India",
            "full_name": "CSIR-Institute of Microbial Technology",
            "webpage": "http://www.imtech.res.in/"
          }
        ],
        "contributor_name": "Komal",
        "contributor_surname": "Choukate",
        "orcid": ""
      }
    ],
    "concentration_method": null,
    "concentration_unit": null,
    "date": "2017-12-15",
    "storage_temperature": 4.0,
    "cell_temperature": 4.0,
    "exposure_time": 1.0,
    "number_of_frames": 10,
    "wavelength": 0.1,
    "sample_detector_distance": 2.87,
    "concentration_min": null,
    "concentration_max": 2.7,
    "sample_volume": null,
    "flow_rate": null,
    "s_min": 0.039,
    "s_max": 4.934,
    "total_exposure_time": null,
    "seccolumn": null
  },
  "fits": [],
  "estimated_volume_method": null,
  "pddf_software": "ATSAS GNOM",
  "pddf_software_version": "4.6",
  "i0_calibration_standard": null,
  "description": "The cell wall synthesis protein Wag31: Polymer tbWag31 T73A forms a large super-macromolecular assembly (supported by atomic force microscopy, AFM) and as a result there is a very limited angular range to estimate the radius of gyration, Rg, using the Guinier approximation. In addition, the quoted monomer molecular weight does not apply to this sample. The probable distribution of real-space scattering pair vector lengths (p(r) vs r profile or PDDF) represents the cross-sectional pair distribution function for rod-like particle (option 4 in GNOM) and the subsequent data validation tools for this entry are based on the corresponding cross section parameters (Rg of cross section and Dmax of cross section). The I(s) is recorded in a relative scale in kDa units assuming a 1 mg/ml sample concentration. However the experimental concentration was found to be 2.7 mg/ml (assessed using a Bradford assay).",
  "experiment_description": "Synchrotron SAXS data from solutions of the polymeric form of Wag31 T73A in 50mM Tris, 300mM NaCl, 10% glycerol, 1mM EDTA (ethylene diamine tetra acetic acid), 5mM β-mercaptoethanol (BME), pH 7.5 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 = 0.1 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 2.70 mg/ml was measured at 4°C. 10 successive 1 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.",
  "tags": [],
  "intensity_unit": "arbitrary",
  "experimental_mw": 29.9,
  "experimental_mw_error": null,
  "guinier_i0_mw": null,
  "guinier_i0_mw_error": null,
  "porod_mw": null,
  "porod_mw_error": null,
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  "guinier_i0": 990.33,
  "guinier_i0_error": 17.9,
  "pddf_rg": 3.32,
  "pddf_rg_error": 0.021,
  "guinier_rg": 21.8,
  "guinier_rg_error": 0.409,
  "pddf_dmax": 13.55,
  "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": 6,
  "pddf_point_first": null,
  "pddf_point_last": null,
  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDEC2_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2020-08-13T15:33:49.909979+02:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
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