SASDBG6

Ribosome biogenesis protein 15 (Nop15)

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
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Ribosome biogenesis protein 15 (Nop15)

浓度0.7 – 3.0 缓冲液 / pH25 mM HEPES, 500 mM NaCl, 2 mM DTT / 7.5
实验温度4.0 设备 / 束线Advanced Light Source (ALS) / 12.3.1 (SIBYLS)
波长0.1 nm曝光0.5 s × 1

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Ribosome biogenesis protein 15
查看序列
KDKKTLEEYSGIIYVSRLPHGFHEKELSKYFAQFGDLKEVRLARNKKTGNSRHYGFLEFVNKEDAMIAQESMNNYLLMGHLLQVRVLPKGAKIEKLYKYKKRVLVEKGITKPVKQLKDNMKQKHEERIKKLAKSGIEFKW
proteinSaccharomyces cerevisiaeP5392781–220monomer分子数 116.541 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
1451[3]0.019764–0.293394 1/A含误差列缺失 00sasbdb/entries/g6/sasdbg6/source/SASDBG6.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)10.3—Å
i0Guinier113.763.6—
i0P(r)125.63.5—
mwExperimental16.4—kDa
mwPorod23.0—kDa
porod_volumePorod38.0—ų
rgGuinier2.40.09Å
rgP(r)2.860.09Å

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25 mM HEPES, 500 mM NaCl, 2 mM DTT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2013-04-25储存 / 测量温度4.0 / 4.0
曝光时间0.5帧数1
波长0.1样品-探测器距离—
光源X-ray synchrotron探测器MAR 165 CCD
机构 / 束线Advanced Light Source (ALS) / 12.3.1 (SIBYLS) · Berkeley, CA, USA
q 范围0.198 – 2.934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
curvesasbdb/entries/g6/sasdbg6/source/SASDBG6.datdownloaded1874197709b6a1d75387f6db09cec84c17a39088a7889dd7bcbf3ac3783d77d209b61下载查看原文件源站
full_entry_zipsasbdb/entries/g6/sasdbg6/source/SASDBG6.zipdownloaded60323f46abfd36367e16abe4902e09e5d0c507a9956382f23c760925c7e1a8819dc85下载查看原文件源站
pddfsasbdb/entries/g6/sasdbg6/source/SASDBG6.outdownloaded43837290b16990e51dfd2412d199d7d31830b98f5b29280b25649af5449627a15183d下载查看原文件源站
sascifsasbdb/entries/g6/sasdbg6/source/SASDBG6.sascifdownloaded2862501c177c409cc00a946f3f988107d7f49765f95753640a626549b1cb5db0c59d5f下载查看原文件源站
summarysasbdb/entries/g6/sasdbg6/source/summary.jsondownloaded8747db22d3e057c4161182e588d7590b212636946b515c37241a53a0e8d15b0fd809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(6 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:185 个字段值
字段路径原始值
codeSASDBG6
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleStructural analysis reveals the flexible C-terminus of Nop15 undergoes rearrangement to recognize a pre-ribosomal RNA folding intermediate.
project.publication.titleStructural analysis reveals the flexible C-terminus of Nop15 undergoes rearrangement to recognize a pre-ribosomal RNA folding intermediate.
project.publication.author_listZhang J, Gonzalez LE, Hall TMT
project.publication.journalNucleic Acids Res
project.publication.doi10.1093/nar/gkw961
project.publication.pmid27789691
project.publication.published_date2017 Mar 17
project.statusreleased
project.submitted_date2016-09-18
project.released_date2017-04-05
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDBG6.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDBG6.dat
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sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDBG6.sascif
experiment.instrument.detector.typenull
experiment.instrument.detector.nameMAR 165 CCD
experiment.instrument.detector.resolutionnull
experiment.instrument.nameAdvanced Light Source (ALS)
experiment.instrument.cityBerkeley, CA
experiment.instrument.countryUSA
experiment.instrument.beamline_name12.3.1 (SIBYLS)
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_nameRibosome biogenesis protein 15
experiment.sample.molecule[0].short_nameNop15
experiment.sample.molecule[0].sequenceKDKKTLEEYS GIIYVSRLPH GFHEKELSKY FAQFGDLKEV RLARNKKTGN SRHYGFLEFV NKEDAMIAQE SMNNYLLMGH LLQVRVLPKG AKIEKLYKYK KRVLVEKGIT KPVKQLKDNMKQKHEERIKK LAKSGIEFKW
experiment.sample.molecule[0].organismSaccharomyces cerevisiae
experiment.sample.molecule[0].uniprot_codeP53927
experiment.sample.molecule[0].uniprot_range_first81
experiment.sample.molecule[0].uniprot_range_last220
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMVKSTSKTSTKETVTKQPTEEKPIQEKEELALETSSSSSDEEDEKDEDEIEGLAASDDEQ SGTHKIKRLNPKKQANEKKSKDKKTLEEYSGIIYVSRLPHGFHEKELSKYFAQFGDLKEV RLARNKKTGNSRHYGFLEFVNKEDAMIAQESMNNYLLMGHLLQVRVLPKGAKIEKLYKYK KRVLVEKGITKPVKQLKDNMKQKHEERIKKLAKSGIEFKW
experiment.sample.molecule[0].mw16.541
experiment.sample.molecule[0].total_mw16.541
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.buffer.name25 mM HEPES, 500 mM NaCl, 2 mM DTT
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameRibosome biogenesis protein 15 (Nop15)
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_nameNIH
experiment.contributor[0].affiliation[0].addressBethesda, Maryland, USA
experiment.contributor[0].affiliation[0].full_nameNational Institutes of Health, Bethesda, MD
experiment.contributor[0].affiliation[0].webpagehttps://www.nih.gov/
experiment.contributor[0].contributor_nameJun
experiment.contributor[0].contributor_surnameZhang
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2013-04-25
experiment.storage_temperature4.0
experiment.cell_temperature4.0
experiment.exposure_time0.5
experiment.number_of_frames1
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experiment.flow_ratenull
experiment.s_min0.198
experiment.s_max2.934
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].models[0].softwareEOM/RANCH
fits[0].models[0].pdb_link[0].pdb_code5t9p
fits[0].models[0].pdb_link[0].ext_code5T9P
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fits[0].softwarenull
fits[0].chi_square_value0.649
fits[0].p_value0.0
fits[0].fit_residual_plotfit4columns497_fitresiduals_img.png
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fits[0].fit_lognull
fits[0].software_versionnull
fits[0].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versionGNOM 5
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of ribosome biogenesis protein 15 (Nop15) in 25 mM HEPES, 500 mM NaCl, 2 mM DTT, pH 7.5 were collected on the BL 12.3.1 (SIBYLS) beam line at the Advanced Light Source (ALS, Berkeley, CA, USA) using a MAR Image Plate detector at a wavelength of λ = 0.1 nm (I(s) vs s, where s = 4π sin θ/λ, and 2θ is the scattering angle). Solute concentrations ranging between 0.7 and 3 mg/ml were measured at 4 °C (the data displayed in this entry: 0.7 mg/ml). One 0.5 second frame was collected per sample. The data were normalized to the intensity of the transmitted beam, radially averaged and the scattering of the solvent-blank was subtracted.
tags[]
intensity_unitnull
experimental_mw16.4
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw23.0
porod_mw_errornull
pddf_i0125.6
pddf_i0_error3.5
guinier_i0113.76
guinier_i0_error3.6
pddf_rg2.86
pddf_rg_error0.09
guinier_rg2.4
guinier_rg_error0.09
pddf_dmax10.3
pddf_dmax_errornull
porod_volume38.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first27
guinier_point_last56
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDBG6_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
codeSASDBG6
statussuccess
started_at2026-08-11T15:09:27.618909+00:00
finished_at2026-08-11T15:09:38.905916+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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查看完整 summary.json 原文
{
  "code": "SASDBG6",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Structural analysis reveals the flexible C-terminus of Nop15 undergoes rearrangement to recognize a pre-ribosomal RNA folding intermediate.",
    "publication": {
      "title": "Structural analysis reveals the flexible C-terminus of Nop15 undergoes rearrangement to recognize a pre-ribosomal RNA folding intermediate.",
      "author_list": "Zhang J, Gonzalez LE, Hall TMT",
      "journal": "Nucleic Acids Res",
      "doi": "10.1093/nar/gkw961",
      "pmid": "27789691",
      "published_date": "2017 Mar 17"
    },
    "status": "released",
    "submitted_date": "2016-09-18",
    "released_date": "2017-04-05"
  },
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    },
    "sample": {
      "molecule": [
        {
          "long_name": "Ribosome biogenesis protein 15",
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          "sequence": "KDKKTLEEYS GIIYVSRLPH GFHEKELSKY FAQFGDLKEV RLARNKKTGN SRHYGFLEFV NKEDAMIAQE \r\nSMNNYLLMGH LLQVRVLPKG AKIEKLYKYK KRVLVEKGIT KPVKQLKDNMKQKHEERIKK LAKSGIEFKW",
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            "address": "Bethesda, Maryland, USA",
            "full_name": "National Institutes of Health, Bethesda, MD",
            "webpage": "https://www.nih.gov/"
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}
查看完整 manifest.json 原文
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