SASDBY5

C-terminal fragment (509-716) of the Methoprene-tolerant protein from Drosophila melanogaster

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2023-06-21T07:56:39.492710+02:00

Modelling of the MetC low resolution structure was performed using Ensemble Optimization Method (EOM), of which selected models are displayed in this entry. The full results obtained from EOM modelling that includes the optimised Rg and size distributions of the MetC ensemble are included in the full entry zip archive. Note: The C-terminal fragment of the MetC protein (residues 509-716) has nine additional amino acids (GSGGIEGRH) at the N-terminus derived from the affinity tag encoded in the pColdTF expression plasmid (remaining after protease cleavage). The molecular weight (from I(0)) was calculated from the SAXS data by scaling the intensities by 0.3 in order to match the high-q scattering intensities obtained from a BSA standard. This procedure was done because estimating the concentration the MetC sample is prone to significant errors as a consequence of the protein's poor extinction coefficient (Abs. 280 nm 1mg/ml = 0.130).

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · C-terminal fragment (509-716) of the Methoprene-tolerant protein from Drosophila melanogaster

浓度— – 2.6 缓冲液 / pH20mM Tris/HCl 150mM NaCl / 7.5
实验温度10.0 设备 / 束线PETRA III / EMBL P12
波长0.124 nm曝光0.5 s × 20

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
FI10506p
查看序列
GSGGIEGRHAGRQKVQEMKEKFSTIIKAEMPTQSSSPDLPASQAPQQLERIVLYLIENLQKSVDSAETVGGQGMESLMDDGYSSPANTLTLEELAPSPTPALALVPPAPSSVKSSISKSVSVVNVTAARKFQQEHQKQRERDREQLKERTNSTQGVIRQLSSCLSEAETASCILSPASSLSASEAPDTPDPHSNTSPPPSLHTRPSVLHRTLTSTLR
proteinDrosophila melanogasterQ9VYW2509–716monomer分子数 123.4 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
11816[3]0.022031–4.82037 1/nm含误差列缺失 059sasbdb/entries/y5/sasdby5/source/SASDBY5.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)22.0—nm
i0Guinier38540.0——
i0P(r)397600.0——
mwExperimental30.52—kDa
mwGuinier I(0)30.52—kDa
rgGuinier5.1—nm
rgP(r)5.61—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20mM Tris/HCl 150mM NaCl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2015-07-21储存 / 测量温度— / 10.0
曝光时间0.5帧数20
波长0.124样品-探测器距离3.0
光源X-ray synchrotron探测器Pilatus 2M
机构 / 束线PETRA III / EMBL P12 · DESY; Hamburg, Germany
q 范围0.022 – 4.82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(8 项)
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pddf: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:169 个字段值
字段路径原始值
codeSASDBY5
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleIntrinsic Disorder of the C-Terminal Domain of Drosophila Methoprene-Tolerant Protein.
project.publication.titleIntrinsic Disorder of the C-Terminal Domain of Drosophila Methoprene-Tolerant Protein.
project.publication.author_listKolonko M, Ożga K, Hołubowicz R, Taube M, Kozak M, Ożyhar A, Greb-Markiewicz B
project.publication.journalPLoS One
project.publication.doi10.1371/journal.pone.0162950
project.publication.pmid27657508
project.publication.published_date2016
project.statusreleased
project.submitted_date2016-08-26
project.released_date2016-09-05
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experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus 2M
experiment.instrument.detector.resolutionnull
experiment.instrument.namePETRA III
experiment.instrument.cityDESY; Hamburg
experiment.instrument.countryGermany
experiment.instrument.beamline_nameEMBL P12
experiment.instrument.beam_geometrynull
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_nameFI10506p
experiment.sample.molecule[0].short_nameMet
experiment.sample.molecule[0].sequenceGSGGIEGRHAGRQKVQEMKEKFSTIIKAEMPTQSSSPDLPA SQAPQQLERIVLYLIENLQKSVDSAETVGGQGMESLMDDGYSSPANTLTLEELAPSPTPA LALVPPAPSSVKSSISKSVSVVNVTAARKFQQEHQKQRERDREQLKERTNSTQGVIRQLS SCLSEAETASCILSPASSLSASEAPDTPDPHSNTSPPPSLHTRPSVLHRTLTSTLR
experiment.sample.molecule[0].organismDrosophila melanogaster
experiment.sample.molecule[0].uniprot_codeQ9VYW2
experiment.sample.molecule[0].uniprot_range_first509
experiment.sample.molecule[0].uniprot_range_last716
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMAAPETGNTGSTGSAGSTGSGSGSGSGSGSSSDPANGREARNLAEKQRRDKLNASIQELA TMVPHAAESSRRLDKTAVLRFATHGLRLQYVFGKSASRRRKKTGLKGTGMSASPVGDLPN PSLHLTDTLMQLLDCCFLTLTCSGQIVLVSTSVEQLLGHCQSDLYGQNLLQITHPDDQDL LRQQLIPRDIETLFYQHQHHQQQGHNPQQHSTSTSASTSGSDLEEEEMETEEHRLGRQQG EADDDEDHPYNRRTPSPRRMAHLATIDDRLRMDRRCFTVRLARASTRAEATRHYERVKID GCFRRSDSSLTGGAAANYPIVSQLIRRSRNNNMLAAAAAVAAEAATVPPQHDAIAQAALH GISGNDIVLVAMARVLREERPPEETEGTVGLTIYRQPEPYQLEYHTRHLIDGSIIDCDQR IGLVAGYMKDEVRNLSPFCFMHLDDVRWVIVALRQMYDCNSDYGESCYRLLSRNGRFIYL HTKGFLEVDRGSNKVHSFLCVNTLLDEEAGRQKVQEMKEKFSTIIKAEMPTQSSSPDLPA SQAPQQLERIVLYLIENLQKSVDSAETVGGQGMESLMDDGYSSPANTLTLEELAPSPTPA LALVPPAPSSVKSSISKSVSVVNVTAARKFQQEHQKQRERDREQLKERTNSTQGVIRQLS SCLSEAETASCILSPASSLSASEAPDTPDPHSNTSPPPSLHTRPSVLHRTLTSTLR
experiment.sample.molecule[0].mw23.4
experiment.sample.molecule[0].total_mw23.4
experiment.sample.molecule[0].number_molecules1
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
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experiment.sample.buffer.name20mM Tris/HCl 150mM NaCl
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
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experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.5
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experiment.sample.purity_methodnull
experiment.sample.nameC-terminal fragment (509-716) of the Methoprene-tolerant protein from Drosophila melanogaster
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_nameAMU
experiment.contributor[0].affiliation[0].addressPoznań, Poland
experiment.contributor[0].affiliation[0].full_nameAdam Mickiewicz University in Poznań
experiment.contributor[0].affiliation[0].webpagehttps://international.amu.edu.pl/
experiment.contributor[0].contributor_nameMichal
experiment.contributor[0].contributor_surnameTaube
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2015-07-21
experiment.storage_temperaturenull
experiment.cell_temperature10.0
experiment.exposure_time0.5
experiment.number_of_frames20
experiment.wavelength0.124
experiment.sample_detector_distance3.0
experiment.concentration_minnull
experiment.concentration_max2.6
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.022
experiment.s_max4.82
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versionnull
i0_calibration_standardnull
descriptionModelling of the MetC low resolution structure was performed using Ensemble Optimization Method (EOM), of which selected models are displayed in this entry. The full results obtained from EOM modelling that includes the optimised Rg and size distributions of the MetC ensemble are included in the full entry zip archive. Note: The C-terminal fragment of the MetC protein (residues 509-716) has nine additional amino acids (GSGGIEGRH) at the N-terminus derived from the affinity tag encoded in the pColdTF expression plasmid (remaining after protease cleavage). The molecular weight (from I(0)) was calculated from the SAXS data by scaling the intensities by 0.3 in order to match the high-q scattering intensities obtained from a BSA standard. This procedure was done because estimating the concentration the MetC sample is prone to significant errors as a consequence of the protein's poor extinction coefficient (Abs. 280 nm 1mg/ml = 0.130).
experiment_descriptionSynchrotron SAXS data from solutions of the C-terminal fragment (509-716) of the Methoprene-tolerant protein from Drosophila melanogaster in 20mM Tris/HCl, 150mM NaCl, pH 7.5 were collected on the P12 beam line at Petra-III (Hamburg, Germany) using a Pilatus 2M detector at a wavelength of λ = 0.124 nm (I(s) vs s where s = 4π sin θ/λ and 2θ is the scattering angle). One solute concentration of 2.60 mg/ml was measured. 20 successive 0.500 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 and the data scaled to protein concentration. The low angle data collected were obtained from a single concentration scattering curve.
tags[0]idp
intensity_unitnull
experimental_mw30.52
experimental_mw_errornull
guinier_i0_mw30.52
guinier_i0_mw_errornull
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intensities_log_log_plotSASDBY5_datloglog_img.png
symmetrynull
last_modified2023-06-21T07:56:39.492710+02:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDBY5
statussuccess
started_at2026-08-11T14:58:53.913182+00:00
finished_at2026-08-11T14:59:02.896392+00:00
source_last_modified2023-06-21T07:56:39.492710+02:00
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查看完整 summary.json 原文
{
  "code": "SASDBY5",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
  "project": {
    "title": "Intrinsic Disorder of the C-Terminal Domain of Drosophila Methoprene-Tolerant Protein.",
    "publication": {
      "title": "Intrinsic Disorder of the C-Terminal Domain of Drosophila Methoprene-Tolerant Protein.",
      "author_list": "Kolonko M, Ożga K, Hołubowicz R, Taube M, Kozak M, Ożyhar A, Greb-Markiewicz B",
      "journal": "PLoS One",
      "doi": "10.1371/journal.pone.0162950",
      "pmid": "27657508",
      "published_date": "2016"
    },
    "status": "released",
    "submitted_date": "2016-08-26",
    "released_date": "2016-09-05"
  },
  "pddf_data": "https://www.sasbdb.org/media/p_of_R_files/SASDBY5.out",
  "intensities_data": "https://www.sasbdb.org/media/intensities_files/SASDBY5.dat",
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  "sascif_data": "https://www.sasbdb.org/media/sascif/sascif_files/SASDBY5.sascif",
  "experiment": {
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      "detector": {
        "type": null,
        "name": "Pilatus 2M",
        "resolution": null
      },
      "name": "PETRA III",
      "city": "DESY; Hamburg",
      "country": "Germany",
      "beamline_name": "EMBL P12",
      "beam_geometry": null,
      "type_of_source": "X-ray synchrotron",
      "point_source": null,
      "line_collimation": null,
      "sample_path_length": null,
      "line_collimation_slitlength": null,
      "line_collimation_integrationwidth": null,
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    },
    "sample": {
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        {
          "long_name": "FI10506p",
          "short_name": "Met",
          "sequence": "GSGGIEGRHAGRQKVQEMKEKFSTIIKAEMPTQSSSPDLPA\r\nSQAPQQLERIVLYLIENLQKSVDSAETVGGQGMESLMDDGYSSPANTLTLEELAPSPTPA\r\nLALVPPAPSSVKSSISKSVSVVNVTAARKFQQEHQKQRERDREQLKERTNSTQGVIRQLS\r\nSCLSEAETASCILSPASSLSASEAPDTPDPHSNTSPPPSLHTRPSVLHRTLTSTLR",
          "organism": "Drosophila melanogaster",
          "uniprot_code": "Q9VYW2",
          "uniprot_range_first": 509,
          "uniprot_range_last": 716,
          "oligomerization": "monomer",
          "molecular_type": "protein",
          "uniprot_sequence": "MAAPETGNTGSTGSAGSTGSGSGSGSGSGSSSDPANGREARNLAEKQRRDKLNASIQELA\nTMVPHAAESSRRLDKTAVLRFATHGLRLQYVFGKSASRRRKKTGLKGTGMSASPVGDLPN\nPSLHLTDTLMQLLDCCFLTLTCSGQIVLVSTSVEQLLGHCQSDLYGQNLLQITHPDDQDL\nLRQQLIPRDIETLFYQHQHHQQQGHNPQQHSTSTSASTSGSDLEEEEMETEEHRLGRQQG\nEADDDEDHPYNRRTPSPRRMAHLATIDDRLRMDRRCFTVRLARASTRAEATRHYERVKID\nGCFRRSDSSLTGGAAANYPIVSQLIRRSRNNNMLAAAAAVAAEAATVPPQHDAIAQAALH\nGISGNDIVLVAMARVLREERPPEETEGTVGLTIYRQPEPYQLEYHTRHLIDGSIIDCDQR\nIGLVAGYMKDEVRNLSPFCFMHLDDVRWVIVALRQMYDCNSDYGESCYRLLSRNGRFIYL\nHTKGFLEVDRGSNKVHSFLCVNTLLDEEAGRQKVQEMKEKFSTIIKAEMPTQSSSPDLPA\nSQAPQQLERIVLYLIENLQKSVDSAETVGGQGMESLMDDGYSSPANTLTLEELAPSPTPA\nLALVPPAPSSVKSSISKSVSVVNVTAARKFQQEHQKQRERDREQLKERTNSTQGVIRQLS\nSCLSEAETASCILSPASSLSASEAPDTPDPHSNTSPPPSLHTRPSVLHRTLTSTLR",
          "mw": 23.4,
          "total_mw": 23.4,
          "number_molecules": 1,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
      ],
      "buffer": {
        "name": "20mM Tris/HCl 150mM NaCl",
        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 7.5,
        "deuteration": null
      },
      "purity_method": null,
      "name": "C-terminal fragment (509-716) of the Methoprene-tolerant protein from Drosophila melanogaster",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": "AMU",
            "address": "Poznań, Poland",
            "full_name": "Adam Mickiewicz University in Poznań",
            "webpage": "https://international.amu.edu.pl/"
          }
        ],
        "contributor_name": "Michal",
        "contributor_surname": "Taube",
        "orcid": null
      }
    ],
    "concentration_method": null,
    "concentration_unit": null,
    "date": "2015-07-21",
    "storage_temperature": null,
    "cell_temperature": 10.0,
    "exposure_time": 0.5,
    "number_of_frames": 20,
    "wavelength": 0.124,
    "sample_detector_distance": 3.0,
    "concentration_min": null,
    "concentration_max": 2.6,
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    "flow_rate": null,
    "s_min": 0.022,
    "s_max": 4.82,
    "total_exposure_time": null,
    "seccolumn": null
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        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDBY5_fit1_model1_img.png",
          "software": "EOM/RANCH",
          "pdb_link": [],
          "model_title": null,
          "type_of_model": "dummy",
          "software_version": "",
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDBY5_fit1_model1.pdb",
          "model_mw": null,
          "bead_radius": 1.9,
          "log": null,
          "symmetry": "",
          "comment": "",
          "user": 148
        },
        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDBY5_fit1_model2_img.png",
          "software": "EOM/RANCH",
          "pdb_link": [],
          "model_title": null,
          "type_of_model": "dummy",
          "software_version": "",
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDBY5_fit1_model2.pdb",
          "model_mw": null,
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          "log": null,
          "symmetry": "",
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      ],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDBY5_fit1_fixed_fit_img.png",
      "software": null,
      "chi_square_value": 0.962361,
      "p_value": 0.7654,
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      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDBY5_fit1.fit",
      "fit_log": null,
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  "estimated_volume_method": null,
  "pddf_software": "ATSAS GNOM",
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  "description": "Modelling of the MetC low resolution structure was performed using Ensemble Optimization Method (EOM), of which selected models are displayed in this entry. The full results obtained from EOM modelling that includes the optimised Rg and size distributions of the MetC ensemble are included in the full entry zip archive. \r\nNote: The C-terminal fragment of the MetC protein (residues 509-716) has nine additional amino acids (GSGGIEGRH) at the N-terminus derived from the affinity tag encoded in the pColdTF expression plasmid (remaining after protease cleavage). The molecular weight (from I(0)) was calculated from the SAXS data by scaling the intensities by 0.3 in order to match the high-q scattering intensities obtained from a BSA standard. This procedure was done because estimating the concentration the MetC sample is prone to significant errors as a consequence of the protein's poor extinction coefficient (Abs. 280 nm 1mg/ml = 0.130).",
  "experiment_description": "Synchrotron SAXS data from solutions of the C-terminal fragment (509-716) of the Methoprene-tolerant protein from Drosophila melanogaster in 20mM Tris/HCl, 150mM NaCl, pH 7.5 were collected on the P12 beam line at Petra-III (Hamburg, Germany) using a Pilatus 2M detector at a wavelength of λ = 0.124 nm (I(s) vs s where s = 4π sin θ/λ and 2θ is the scattering angle). One solute concentration of 2.60 mg/ml was measured. 20 successive 0.500 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 and the data scaled to protein concentration. The low angle data collected were obtained from a single concentration scattering curve.",
  "tags": [
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  "pddf_dmax_error": null,
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  "guinier_point_first": null,
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  "pddf_point_first": null,
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  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDBY5_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2023-06-21T07:56:39.492710+02:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
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