SASDFG8

Glutamine-binding periplasmic protein with hexahistidine tag (GlnBP) in the presence of glutamine - Gln-bound 10-fold excess

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2019-12-06T13:07:15.624532+01:00

Gln-bound GlnBP at a ligand:protein ratio of 10:1. Ligand condition is prepared by dissolving glutamine in powder form (Sigma-Aldrich) directly into the SAXS buffer, followed by dilution to the target concentration with additional SAXS buffer.

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Glutamine-binding periplasmic protein with hexahistidine tag (GlnBP) in the presence of glutamine - Gln-bound 10-fold excess

浓度— – 2.0 缓冲液 / pH100 mM NaCl, 20 mM NaPO4, 0.5 mM TCEP / 7.4
实验温度20.0 设备 / 束线ESRF / BM29
波长0.09919 nm曝光2.0 s × 12

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Glutamine-binding periplasmic protein with hexahistidine tag
查看序列
HHHHHHADKKLVVATDTAFVPFEFKQGDKYVGFDVDLWAAIAKELKLDYELKPMDFSGIIPALQTKNVDLALAGITITDERKKAIDFSDGYYKSGLLVMVKANNNDVKSVKDLDGKVVAVKSGTGSVDYAKANIKTKDLRQFPNIDNAYMELGTNRADAVLHDTPNILYFIKTAGNGQFKAVGDSLEAQQYGIAFPKGSDELRDKVNGALKTLRENGTYNEIYKKWFGTEPK
proteinEscherichia coliP0AEQ323–248monomer分子数 125.786 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]0.03059113–4.946227 1/nm含误差列缺失 019sasbdb/entries/g8/sasdfg8/source/SASDFG8.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)6.1—nm
i0Guinier49.650.06arbitrary
i0P(r)49.47—arbitrary
mwExperimental25.0—kDa
mwPorod21.0—kDa
porod_volumePorod34.0—nm³
rgGuinier2.030.13nm
rgP(r)2.023—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

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100 mM NaCl, 20 mM NaPO4, 0.5 mM TCEP缓冲液浓度—
pH7.4添加剂—
缓冲液说明SEC buffer for PBP experiments
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2018-09-10储存 / 测量温度— / 20.0
曝光时间2.0帧数12
波长0.09919样品-探测器距离2.849
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线ESRF / BM29 · Grenoble, France
q 范围0.031 – 4.946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(2 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:134 个字段值
字段路径原始值
codeSASDFG8
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleStructure-based screening of binding affinities via small-angle X-ray scattering
project.publication.titleStructure-based screening of binding affinities via small-angle X-ray scattering
project.publication.author_listChen P, Masiewicz P, Perez K, Hennig J
project.publication.journalnull
project.publication.doi10.1101/715193
project.publication.pmidnull
project.publication.published_date2019 Jul 31
project.statusreleased
project.submitted_date2019-07-01
project.released_date2019-08-02
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experiment.instrument.detector.resolution172.0
experiment.instrument.nameESRF
experiment.instrument.cityGrenoble
experiment.instrument.countryFrance
experiment.instrument.beamline_nameBM29
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experiment.sample.molecule[0].long_nameGlutamine-binding periplasmic protein with hexahistidine tag
experiment.sample.molecule[0].short_nameGlnBP
experiment.sample.molecule[0].sequenceHHHHHHADKKLVVATDTAFVPFEFKQGDKYVGFDVDLWAAIAKELKLDYELKPMDFSGIIPALQTK NVDLALAGITITDERKKAIDFSDGYYKSGLLVMVKANNNDVKSVKDLDGKVVAVKSGTGS VDYAKANIKTKDLRQFPNIDNAYMELGTNRADAVLHDTPNILYFIKTAGNGQFKAVGDSL EAQQYGIAFPKGSDELRDKVNGALKTLRENGTYNEIYKKWFGTEPK
experiment.sample.molecule[0].organismEscherichia coli
experiment.sample.molecule[0].uniprot_codeP0AEQ3
experiment.sample.molecule[0].uniprot_range_first23
experiment.sample.molecule[0].uniprot_range_last248
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
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experiment.sample.molecule[0].mw25.786
experiment.sample.molecule[0].total_mw25.786
experiment.sample.molecule[0].number_molecules1
experiment.sample.molecule[0].complex_stateFalse
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experiment.sample.buffer.concentration_unitnull
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experiment.sample.buffer.ph7.4
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experiment.sample.nameGlutamine-binding periplasmic protein with hexahistidine tag (GlnBP) in the presence of glutamine - Gln-bound 10-fold excess
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experiment.sample.contrastnull
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experiment.contributor[0].affiliation[0].short_nameEMBL
experiment.contributor[0].affiliation[0].addressHeidelberg, Germany
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experiment.contributor[0].affiliation[0].webpagehttps://www.embl.de/
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fits[]
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionGln-bound GlnBP at a ligand:protein ratio of 10:1. Ligand condition is prepared by dissolving glutamine in powder form (Sigma-Aldrich) directly into the SAXS buffer, followed by dilution to the target concentration with additional SAXS buffer.
experiment_descriptionSynchrotron SAXS data from solutions of GlnBP with a 10-fold excess of glutamine in 100 mM NaCl, 20 mM NaPO4, 0.5 mM TCEP, 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 2.8 m and at a wavelength of λ = 0.09919 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 2.00 mg/ml was measured at 20°C. 12 successive 2 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[]
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intensities_log_log_plotSASDFG8_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
codeSASDFG8
statussuccess
started_at2026-08-11T15:53:00.749095+00:00
finished_at2026-08-11T15:53:09.013755+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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查看完整 summary.json 原文
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  "status": "Published",
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  "angular_unit": "1/nm",
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    "title": "Structure-based screening of binding affinities via small-angle X-ray scattering",
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      "journal": null,
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      "pmid": null,
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  "i0_calibration_standard": null,
  "description": "Gln-bound GlnBP at a ligand:protein ratio of 10:1. Ligand condition is prepared by dissolving glutamine in powder form (Sigma-Aldrich) directly into the SAXS buffer, followed by dilution to the target concentration with additional SAXS buffer.",
  "experiment_description": "Synchrotron SAXS data from solutions of GlnBP with a 10-fold excess of glutamine in 100 mM NaCl, 20 mM NaPO4, 0.5 mM TCEP, 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 2.8 m and at a wavelength of λ = 0.09919 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 2.00 mg/ml was measured at 20°C. 12 successive 2 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",
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  "experimental_mw_error": null,
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  "guinier_i0_mw_error": null,
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  "guinier_i0": 49.65,
  "guinier_i0_error": 0.06,
  "pddf_rg": 2.023,
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  "guinier_rg_error": 0.13,
  "pddf_dmax": 6.1,
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  "porod_volume": 34.0,
  "porod_volume_error": null,
  "estimated_volume": null,
  "estimated_volume_error": null,
  "guinier_point_first": 15,
  "guinier_point_last": 130,
  "pddf_point_first": null,
  "pddf_point_last": null,
  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDFG8_datloglog_img.png",
  "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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