SASDCK4

Truncated P5abc subdomain from tetrahymena ribozyme: Static 0.25mM MgCl2

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Extrapolated to infinite dilution 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 · Truncated P5abc subdomain from tetrahymena ribozyme: Static 0.25mM MgCl2

浓度0.75 – 1.5 缓冲液 / pH20mM KCl 0.25mM MgCl2 10mM KMOPS 20uM EDTA / 7.0
实验温度20.0 设备 / 束线Cornell High Energy Synchrotron Source (CHESS) / G1
波长0.109 nm曝光10.0 s × 40

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Truncated P5abc subdomain from tetrahymena ribozyme
查看序列
GGCAGUACCAAGUCGCGAAAGCGAUGGCCUUGCAAAGGGUAUGGUAAUAAGCUGCC
RNA———–—monomer分子数 118.223 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
1281[3]0.012–0.29 1/A含误差列缺失 00sasbdb/entries/k4/sasdck4/source/SASDCK4.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)7.6—Å
i0Guinier138.00.3—
i0P(r)138.00.1—
mwExperimental27.2—kDa
rgGuinier2.430.01Å
rgP(r)2.470.01Å

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20mM KCl 0.25mM MgCl2 10mM KMOPS 20uM EDTA缓冲液浓度—
pH7.0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2016-06-17储存 / 测量温度4.0 / 20.0
曝光时间10.0帧数40
波长0.109样品-探测器距离1.54
光源X-ray synchrotron探测器Finger Lakes CCD
机构 / 束线Cornell High Energy Synchrotron Source (CHESS) / G1 · Ithaca, NY, USA
q 范围0.12 – 2.9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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summarysasbdb/entries/k4/sasdck4/source/summary.jsondownloaded6235f2021788218431332456bb1bef146a6d6d418b06cdb21f67424d00edcda0c316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
codeSASDCK4
statusPublished
type_of_curveExtrapolated to infinite dilution
angular_unit1/A
project.titleRevealing the distinct folding phases of an RNA three-helix junction.
project.publication.titleRevealing the distinct folding phases of an RNA three-helix junction.
project.publication.author_listPlumridge A, Katz AM, Calvey GD, Elber R, Kirmizialtin S, Pollack L
project.publication.journalNucleic Acids Res
project.publication.doi10.1093/nar/gky363
project.publication.pmid29762712
project.publication.published_date2018 Aug 21
project.statusreleased
project.submitted_date2017-06-02
project.released_date2018-05-20
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experiment.instrument.detector.resolution0.0
experiment.instrument.nameCornell High Energy Synchrotron Source (CHESS)
experiment.instrument.cityIthaca, NY
experiment.instrument.countryUSA
experiment.instrument.beamline_nameG1
experiment.instrument.beam_geometry
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
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experiment.instrument.xray_energynull
experiment.instrument.beam_profile_ahnull
experiment.instrument.beam_profile_alnull
experiment.sample.molecule[0].long_nameTruncated P5abc subdomain from tetrahymena ribozyme
experiment.sample.molecule[0].short_nametp5abc
experiment.sample.molecule[0].sequenceGGCAGUACCAAGUCGCGAAAGCGAUGGCCUUGCAAAGGGUAUGGUAAUAAGCUGCC
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].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeRNA
experiment.sample.molecule[0].uniprot_sequencenull
experiment.sample.molecule[0].mw18.223
experiment.sample.molecule[0].total_mw18.223
experiment.sample.molecule[0].number_molecules1
experiment.sample.molecule[0].complex_stateFalse
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experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionnull
experiment.sample.buffer.name20mM KCl 0.25mM MgCl2 10mM KMOPS 20uM EDTA
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
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experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameTruncated P5abc subdomain from tetrahymena ribozyme: Static 0.25mM MgCl2
experiment.sample.ext_coefficientnull
experiment.sample.contrastnull
experiment.sample.specific_volnull
experiment.sample.dry_volnull
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experiment.sample.deuterationnull
experiment.sample.mixturenull
experiment.contributor[0].affiliation[0].short_namenull
experiment.contributor[0].affiliation[0].addressIthaca, NY, United States
experiment.contributor[0].affiliation[0].full_nameCornell University
experiment.contributor[0].affiliation[0].webpagehttps://www.cornell.edu/
experiment.contributor[0].contributor_nameAlex
experiment.contributor[0].contributor_surnamePlumridge
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2016-06-17
experiment.storage_temperature4.0
experiment.cell_temperature20.0
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experiment.seccolumnnull
fits[]
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versionnull
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of Truncated P5abc subdomain from tetrahymena ribozyme: Static 0.25mM MgCl2 in 20mM KCl 0.25mM MgCl2 10mM KMOPS 20uM EDTA, pH 7 were collected on the G1 beam line at the Cornell High Energy Synchrotron Source (CHESS; Ithaca, NY, USA) using a CCD Finger Lakes CCD detector at a sample-detector distance of 1.5 m and at a wavelength of λ = 0.109 nm (I(s) vs s, where s = 4πsinθ/λ and 2θ is the scattering angle). Solute concentrations ranging between 0.8 and 1.5 mg/ml were measured at 20°C. 40 successive 10 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 different curves were scaled for protein concentration. The low angle data collected at lower concentrations were extrapolated to infinite dilution and merged with the higher concentration data to yield the final composite scattering curve.
tags[]
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experimental_mw27.2
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
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guinier_i0138.0
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pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDCK4_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
codeSASDCK4
statussuccess
started_at2026-08-11T14:25:08.162838+00:00
finished_at2026-08-11T14:25:15.681629+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": "Extrapolated to infinite dilution",
  "angular_unit": "1/A",
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      "journal": "Nucleic Acids Res",
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      "pmid": "29762712",
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  "intensities_log_log_plot": "SASDCK4_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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  "started_at": "2026-08-11T14:25:08.162838+00:00",
  "finished_at": "2026-08-11T14:25:15.681629+00:00",
  "source_last_modified": "2019-12-06T13:07:15.624532+01:00",
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}