SASDB68

Immediate Early 3 DNA (ICP4N IE3_19mer)

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Other 最后更新:2019-12-06T13:07:15.624532+01:00
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Immediate Early 3 DNA (ICP4N IE3_19mer)

浓度— – — 缓冲液 / pH20 mM HEPES, 150 mM NaCl / 7.4
实验温度20.0 设备 / 束线ESRF / BM29
波长0.0992 nm曝光1.0 s × —

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Immediate Early 3
查看序列
CCGATCGTCCACACGGAGC
DNA———–—dimer分子数 25.839 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
1564[3]0.0223576–0.339573 1/A含误差列缺失 00sasbdb/entries/68/sasdb68/source/SASDB68.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)6.9—Å
i0Guinier47.860.048—
i0P(r)44.35——
mwExperimental0.0—kDa
rgGuinier1.930.011Å
rgP(r)1.925—Å

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

▶

5. 实验说明与论文 Experiment & Publication

▼

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20 mM HEPES, 150 mM 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2015-11-12储存 / 测量温度20.0 / 20.0
曝光时间1.0帧数—
波长0.0992样品-探测器距离2.9
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线ESRF / BM29 · Grenoble, France
q 范围0.224 – 3.396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/68/sasdb68/source/SASDB68.outdownloaded256948c2a0fde2832f7f3ca7e2332a5347cd07d058d6cb29dc122daa07df7de0421b下载查看原文件源站
sascifsasbdb/entries/68/sasdb68/source/SASDB68.sascifnot_available——下载查看原文件源站
summarysasbdb/entries/68/sasdb68/source/summary.jsondownloaded591967fd40d69a2e9bf413fd5da25d42b6a63a3bf5758b5e22b36f6a4609a8e65ca7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(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
codeSASDB68
statusPublished
type_of_curveOther
angular_unit1/A
project.titleThe herpes viral transcription factor ICP4 forms a novel DNA recognition complex.
project.publication.titleThe herpes viral transcription factor ICP4 forms a novel DNA recognition complex.
project.publication.author_listTunnicliffe RB, Lockhart-Cairns MP, Levy C, Mould AP, Jowitt TA, Sito H, Baldock C, Sandri-Goldin RM, Golovanov AP
project.publication.journalNucleic Acids Res
project.publication.doi10.1093/nar/gkx419
project.publication.pmid28505309
project.publication.published_date2017 Jul 27
project.statusreleased
project.submitted_date2016-11-28
project.released_date2017-05-30
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDB68.dat
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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_nameImmediate Early 3
experiment.sample.molecule[0].short_nameIE3
experiment.sample.molecule[0].sequenceCCGATCGTCCACACGGAGC
experiment.sample.molecule[0].organismnull
experiment.sample.molecule[0].uniprot_codenull
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeDNA
experiment.sample.molecule[0].uniprot_sequencenull
experiment.sample.molecule[0].mw5.839
experiment.sample.molecule[0].total_mw11.678
experiment.sample.molecule[0].number_molecules2
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.name20 mM HEPES, 150 mM 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.nameImmediate Early 3 DNA (ICP4N IE3_19mer)
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_namenull
experiment.contributor[0].affiliation[0].addressManchester, UK
experiment.contributor[0].affiliation[0].full_nameUniversity of Manchester
experiment.contributor[0].affiliation[0].webpagehttp://www.manchester.ac.uk/
experiment.contributor[0].contributor_nameMichael
experiment.contributor[0].contributor_surnameLockhart
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2015-11-12
experiment.storage_temperature20.0
experiment.cell_temperature20.0
experiment.exposure_time1.0
experiment.number_of_framesnull
experiment.wavelength0.0992
experiment.sample_detector_distance2.9
experiment.concentration_minnull
experiment.concentration_maxnull
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.224
experiment.s_max3.396
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[]
estimated_volume_methodnull
pddf_softwareScÅtter
pddf_software_version3.0g
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of Immediate Early 3 DNA (ICP4N IE3_19mer) in 20 mM HEPES, 150 mM NaCl, pH 7.4, were collected using HPLC SEC-SAXS at 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 = 0.0992 nm (I(s) vs s, where s = 4π sin θ/λ and 2θ is the scattering angle). The sample was separated using a Superdex 200 increase 3.2/300 size exclusion chromatography column before exposure to X-rays. 50 µL of IE3_19merwas loaded onto the Superdex column and the eluent was flowed through the SAXS beam at 0.075 mL/min; the buffer used as the background was collected after one SEC column volume. Data were collected at 20°C at one second intervals.
tags[]
intensity_unitnull
experimental_mw0.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i044.35
pddf_i0_errornull
guinier_i047.86
guinier_i0_error0.048
pddf_rg1.925
pddf_rg_errornull
guinier_rg1.93
guinier_rg_error0.011
pddf_dmax6.9
pddf_dmax_errornull
porod_volumenull
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last34
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDB68_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:34 个字段值
字段路径原始值
codeSASDB68
statussuccess
started_at2026-08-11T16:27:33.942168+00:00
finished_at2026-08-11T16:27:40.377044+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",
  "type_of_curve": "Other",
  "angular_unit": "1/A",
  "project": {
    "title": "The herpes viral transcription factor ICP4 forms a novel DNA recognition complex.",
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      "author_list": "Tunnicliffe RB, Lockhart-Cairns MP, Levy C, Mould AP, Jowitt TA, Sito H, Baldock C, Sandri-Goldin RM, Golovanov AP",
      "journal": "Nucleic Acids Res",
      "doi": "10.1093/nar/gkx419",
      "pmid": "28505309",
      "published_date": "2017 Jul 27"
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  "last_modified": "2019-12-06T13:07:15.624532+01:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
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