SASDC84

parDE-like toxin-antitoxin module, EcPaaA2_13-63-HisEcParE2 construct

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Other 最后更新:2020-08-28T15:28:16.357175+02:00
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · parDE-like toxin-antitoxin module, EcPaaA2_13-63-HisEcParE2 construct

浓度— – 12.0 缓冲液 / pH50 mM Tris-HCl, 500 mM NaCl / 7.5
实验温度10.0 设备 / 束线SOLEIL / SWING
波长0.103 nm曝光0.75 s × 250

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Plasmid stabilization protein ParE
查看序列
MGSSHHHHHHSSGLVPRGSHLPVLWLESADTDLDDITSYIARFDIDAAERLWQRLRGCVLPLSEHPYLYPPSDRVPGLREIVAHPNYIILYRVTTSSVEVVNVIHARRQF
proteinEscherichia coliA0A0D7C2L12–92monomer分子数 112.596 kDa
Uncharacterized protein
查看序列
METIEQENSYNEWLRAKVATSLADPRPAIPHDEVERRMAERFAKMRKERSKQ
proteinEscherichia coli O157:H7A0A0F6F6Q913–63monomer分子数 16.231 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
1667[3]0.02378252–0.4002562 1/A含误差列缺失 00sasbdb/entries/84/sasdc84/source/SASDC84.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)9.30.5Å
i0Guinier0.02138630.01—
i0P(r)0.020.01—
mwExperimental21.3—kDa
mwPorod21.0—kDa
porod_volumePorod35.7—ų
rgGuinier2.1580.004Å
rgP(r)2.2430.006Å

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, 500 mM 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2012-02-05储存 / 测量温度10.0 / 10.0
曝光时间0.75帧数250
波长0.103样品-探测器距离1.82
光源X-ray synchrotron探测器AVIEX PCCD170170
机构 / 束线SOLEIL / SWING · Saint-Aubin, France
q 范围0.238 – 4.003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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full_entry_zipsasbdb/entries/84/sasdc84/source/SASDC84.zipdownloaded11798590ddd3812aeedef67e776344e42da3f3b41418faee17dd0ae2aca89ed7f6bc3c下载查看原文件源站
pddfsasbdb/entries/84/sasdc84/source/SASDC84.outdownloaded637803afe143d29b98930482d1499f0779c3788270897c9c83685e2cb89bf6d7c246e下载查看原文件源站
sascifsasbdb/entries/84/sasdc84/source/SASDC84.sascifdownloaded620894b4cac34669cc73dfb69e2021ea115666dcebd95677964ab22372b51ac533f114下载查看原文件源站
summarysasbdb/entries/84/sasdc84/source/summary.jsondownloaded9144f3e0f7b0c67e0b289f1e701c2132381a852767ad5dc9276255ed018a7c91e407下载查看原文件源站
curve:来源记录
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full_entry_zip:来源记录与 ZIP 内部目录(7 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:199 个字段值
字段路径原始值
codeSASDC84
statusPublished
type_of_curveOther
angular_unit1/A
project.titleA unique hetero-hexadecameric architecture displayed by the Escherichia coli O157 PaaA2-ParE2 antitoxin-toxin complex.
project.publication.titleA unique hetero-hexadecameric architecture displayed by the Escherichia coli O157 PaaA2-ParE2 antitoxin-toxin complex.
project.publication.author_listSterckx YG, Jové T, Shkumatov AV, Garcia-Pino A, Geerts L, De Kerpel M, Lah J, De Greve H, Van Melderen L, Loris R
project.publication.journalJ Mol Biol
project.publication.doi10.1016/j.jmb.2016.03.007
project.publication.pmid26996937
project.publication.published_date2016 Apr 24
project.statusreleased
project.submitted_date2015-08-24
project.released_date2016-03-18
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experiment.instrument.detector.typeCCD
experiment.instrument.detector.nameAVIEX PCCD170170
experiment.instrument.detector.resolutionnull
experiment.instrument.nameSOLEIL
experiment.instrument.citySaint-Aubin
experiment.instrument.countryFrance
experiment.instrument.beamline_nameSWING
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_namePlasmid stabilization protein ParE
experiment.sample.molecule[0].short_nameParE2
experiment.sample.molecule[0].sequenceMGSSHHHHHHSSGLVPRGSHLPVLWLESADTDLDDITSYIARFDIDAAERLWQRLRGCVLPLSEHPYLYPPSDRVPGLREIVAHPNYIILYRVTTSSVEVVNVIHARRQF
experiment.sample.molecule[0].organismEscherichia coli
experiment.sample.molecule[0].uniprot_codeA0A0D7C2L1
experiment.sample.molecule[0].uniprot_range_first2
experiment.sample.molecule[0].uniprot_range_last92
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMLPVLWLESADTDLDDITSYIARFDIDAAERLWQRLRGCVLPLSEHPYLYPPSDRVPGLR EIVAHPNYIILYRVTTSSVEVVNVIHARRQFP
experiment.sample.molecule[0].mw12.596
experiment.sample.molecule[0].total_mw12.596
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.molecule[1].long_nameUncharacterized protein
experiment.sample.molecule[1].short_namePaaA2
experiment.sample.molecule[1].sequenceMETIEQENSYNEWLRAKVATSLADPRPAIPHDEVERRMAERFAKMRKERSKQ
experiment.sample.molecule[1].organismEscherichia coli O157:H7
experiment.sample.molecule[1].uniprot_codeA0A0F6F6Q9
experiment.sample.molecule[1].uniprot_range_first13
experiment.sample.molecule[1].uniprot_range_last63
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experiment.sample.molecule[1].mw6.231
experiment.sample.molecule[1].total_mw6.231
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experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
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experiment.sample.purity_methodnull
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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_nameVUB
experiment.contributor[0].affiliation[0].addressPleinlaan 2 1050 Brussel
experiment.contributor[0].affiliation[0].full_nameVrije Universiteit Brussel
experiment.contributor[0].affiliation[0].webpagehttp://www.vub.ac.be/
experiment.contributor[0].contributor_nameAlexander
experiment.contributor[0].contributor_surnameShkumatov
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2012-02-05
experiment.storage_temperature10.0
experiment.cell_temperature10.0
experiment.exposure_time0.75
experiment.number_of_frames250
experiment.wavelength0.103
experiment.sample_detector_distance1.82
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experiment.sample_volumenull
experiment.flow_ratenull
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experiment.s_max4.003
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].chi_square_value0.76
fits[0].p_value0.0
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fits[0].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0 (r4547)
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from EcPaaA2_13-63-EcParE2 were collected at the SWING beamline (SOLEIL synchrotron, Gif-sur-Yvette, France) in HPLC mode using a CCD AVIEX detector at a sample-detector distance of 1.8 m and at a wavelength of λ = 0.103 nm (s = 4π sin θ/λ, where 2θ is the scattering angle). Sample was loaded onto a Shodex KW402.5-4F, which was pre-equilibrated with running buffer (50 mM Tris-HCl, 500 mM NaCl, pH 7.5) for at least one column volume. The flow rate was set to 0.2 ml/min. During each HPLC run, 250 frames were collected after 15 min (0.62 CV) using 750 ms per frame and 1500 ms dead time. After radial averaging and buffer subtraction of the data frames using FOXTROT, the scattering curves were processed and analyzed with DATASW.
tags[]
intensity_unitnull
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guinier_i0_mwnull
guinier_i0_mw_errornull
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estimated_volume_errornull
guinier_point_first1
guinier_point_last52
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDC84_datloglog_img.png
symmetrynull
last_modified2020-08-28T15:28:16.357175+02:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDC84
statussuccess
started_at2026-08-11T16:35:50.235645+00:00
finished_at2026-08-11T16:36:03.412427+00:00
source_last_modified2020-08-28T15:28:16.357175+02:00
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查看完整 summary.json 原文
{
  "code": "SASDC84",
  "status": "Published",
  "type_of_curve": "Other",
  "angular_unit": "1/A",
  "project": {
    "title": "A unique hetero-hexadecameric architecture displayed by the Escherichia coli O157 PaaA2-ParE2 antitoxin-toxin complex.",
    "publication": {
      "title": "A unique hetero-hexadecameric architecture displayed by the Escherichia coli O157 PaaA2-ParE2 antitoxin-toxin complex.",
      "author_list": "Sterckx YG, Jové T, Shkumatov AV, Garcia-Pino A, Geerts L, De Kerpel M, Lah J, De Greve H, Van Melderen L, Loris R",
      "journal": "J Mol Biol",
      "doi": "10.1016/j.jmb.2016.03.007",
      "pmid": "26996937",
      "published_date": "2016 Apr 24"
    },
    "status": "released",
    "submitted_date": "2015-08-24",
    "released_date": "2016-03-18"
  },
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查看完整 manifest.json 原文
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