SASDCJ4

Truncated P5abc subdomain from tetrahymena ribozyme: Static 400mM KCl

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 400mM KCl

浓度0.75 – 1.5 缓冲液 / pH400mM KCl 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/j4/sasdcj4/source/SASDCJ4.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)8.0—Å
i0Guinier126.90.5—
i0P(r)127.00.39—
mwExperimental24.7—kDa
rgGuinier2.420.02Å
rgP(r)2.460.01Å

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400mM KCl 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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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
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angular_unit1/A
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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.countryUSA
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experiment.sample.molecule[0].short_nametp5abc
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experiment.contributor[0].affiliation[0].webpagehttps://www.cornell.edu/
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estimated_volume_methodnull
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i0_calibration_standardnull
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experiment_descriptionSynchrotron SAXS data from solutions of Truncated P5abc subdomain from tetrahymena ribozyme: Static 400mM KCl in 400mM KCl 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.
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intensities_log_log_plotSASDCJ4_datloglog_img.png
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last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 个字段值
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codeSASDCJ4
statussuccess
started_at2026-08-11T14:24:30.042966+00:00
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查看完整 summary.json 原文
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}
查看完整 manifest.json 原文
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