SASDD25

1:1 Mixture between Protein sex-lethal mutant (Sxl10GS) and RNA decaneucleotide UGU8

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2020-08-28T15:27:59.704255+02:00

This synchrotron session suffered from misalignment of the beamstop resulting in parasitic scattering at low angles. Note that the uploaded EOM ensemble is chosen as the 2:2-complex with one RNA monomer as fully bound by two Sxl10GS molecules in the canonical position from Protein data bankk (PDB) entry 1B7F.pdb. The second RNA monomer is placed in the canonical position bound to the free RRM2, resulting in three rigid bodies: RRM2+RNA, RRM1+RRM2+RNA, and RRM1.

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · 1:1 Mixture between Protein sex-lethal mutant (Sxl10GS) and RNA decaneucleotide UGU8

浓度— – 1.0 缓冲液 / pH50% dilution of protein buffer {10 mM KP, 50 mM NaCl, 10 mM DTT pH 6} with {milliQ-water pH 7} suspended RNA / 6.0
实验温度20.0 设备 / 束线ESRF / BM29
波长0.09919 nm曝光0.5 s × 10

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Protein sex-lethal mutant
查看序列
>P19339SXL-MUTANT123-294WITHGAMACLEAVAGESITEAND10GSLINKERINSERTEDBETWEEN204-205GAMASNTNLIVNYLPQDMTDRELYALFRAIGPINTCRIMRDYKTGYSFGYAFVDFTSEMDSQRAIKVLNGITVRNKRLKVSYARPGGGSGSGGGGSGESIKDTNLYVTNLPRTITDDQLDTIFGKYGSIVQKNILRDKLTGRPRGVAFVRYNKREEAQEAISALNNVIPEGGSQPLSVRLAEEHGK
proteinDrosophila melanogasterP19339123–294dimer分子数 220.432 kDa
RNA decaneucleotide UGU8
查看序列
>SYNTHETICRNAUGU8UGUUUUUUUU
RNAsynthetic construct——–—dimer分子数 23.119 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
11037[3]0.03082862–4.944437 1/nm含误差列缺失 04sasbdb/entries/25/sasdd25/source/SASDD25.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)8.88—nm
i0Guinier76.650.13arbitrary
i0P(r)77.670.08arbitrary
mwExperimental24.0—kDa
porod_volumePorod40.96—nm³
rgGuinier2.540.07nm
rgP(r)2.630.004nm

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50% dilution of protein buffer {10 mM KP, 50 mM NaCl, 10 mM DTT pH 6} with {milliQ-water pH 7} suspended RNA缓冲液浓度—
pH6.0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2017-04-12储存 / 测量温度20.0 / 20.0
曝光时间0.5帧数10
波长0.09919样品-探测器距离2.867
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线ESRF / BM29 · Grenoble, France
q 范围0.031 – 4.944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/25/sasdd25/source/SASDD25.datdownloaded3467254ec18ccd9f770249a321037c786555d74af4570b1a898379a2b59460ec65fb7下载查看原文件源站
full_entry_zipsasbdb/entries/25/sasdd25/source/SASDD25.zipdownloaded172638a1ac978aaca46f3865b2627b263b4fdc6954a45c2ee91e1faa052561ffd2d18a下载查看原文件源站
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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(7 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:199 个字段值
字段路径原始值
codeSASDD25
statusPublished
type_of_curveSingle concentration
angular_unit1/nm
project.titleA General Small-Angle X-ray Scattering-Based Screening Protocol Validated for Protein-RNA Interactions.
project.publication.titleA General Small-Angle X-ray Scattering-Based Screening Protocol Validated for Protein-RNA Interactions.
project.publication.author_listChen PC, Masiewicz P, Rybin V, Svergun D, Hennig J
project.publication.journalACS Comb Sci
project.publication.doi10.1021/acscombsci.8b00007
project.publication.pmid29553252
project.publication.published_date2018 Apr 9
project.statusreleased
project.submitted_date2018-03-15
project.released_date2018-03-21
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDD25.out
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experiment.instrument.detector.typeDectris
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_nameProtein sex-lethal mutant
experiment.sample.molecule[0].short_nameSxl10GS
experiment.sample.molecule[0].sequence>P19339 Sxl-mutant 123-294 with GAMA cleavage site and 10GS linker inserted between 204-205 GAMASNTNLIVNYLPQDMTDRELYALFRAIGPINTCRIMRDYKTGYSFGYAFVDFTSEMDSQ RAIKVLNGITVRNKRLKVSYARPGGGSGSGGGGSGESIKDTNLYVTNLPRTITDDQLDTIFGKYGSIVQK NILRDKLTGRPRGVAFVRYNKREEAQEAISALNNVIPEGGSQPLSVRLAEEHGK
experiment.sample.molecule[0].organismDrosophila melanogaster
experiment.sample.molecule[0].uniprot_codeP19339
experiment.sample.molecule[0].uniprot_range_first123
experiment.sample.molecule[0].uniprot_range_last294
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMYGNNNPGSNNNNGGYPPYGYNNKSSGGRGFGMSHSLPSGMSRYAFSPQDTEFSFPSSSS RRGYNDFPGCGGSGGNGGSANNLGGGNMCHLPPMASNNSLNNLCGLSLGSGGSDDLMNDP RASNTNLIVNYLPQDMTDRELYALFRAIGPINTCRIMRDYKTGYSFGYAFVDFTSEMDSQ RAIKVLNGITVRNKRLKVSYARPGGESIKDTNLYVTNLPRTITDDQLDTIFGKYGSIVQK NILRDKLTGRPRGVAFVRYNKREEAQEAISALNNVIPEGGSQPLSVRLAEEHGKAKAAHF MSQMGVVPANVPPPPPQPPAHMAAAFNMMHRGRSIKSQQRFQNSHPYFDAKKFI
experiment.sample.molecule[0].mw20.432
experiment.sample.molecule[0].total_mw40.864
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.molecule[1].long_nameRNA decaneucleotide UGU8
experiment.sample.molecule[1].short_nameUGU8
experiment.sample.molecule[1].sequence> Synthetic RNA UGU8 UGUUU UUUUU
experiment.sample.molecule[1].organismsynthetic construct
experiment.sample.molecule[1].uniprot_codenull
experiment.sample.molecule[1].uniprot_range_firstnull
experiment.sample.molecule[1].uniprot_range_lastnull
experiment.sample.molecule[1].oligomerizationdimer
experiment.sample.molecule[1].molecular_typeRNA
experiment.sample.molecule[1].uniprot_sequencenull
experiment.sample.molecule[1].mw3.119
experiment.sample.molecule[1].total_mw6.238
experiment.sample.molecule[1].number_molecules2
experiment.sample.molecule[1].complex_stateFalse
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experiment.sample.molecule[1].molecule_sourcebiological
experiment.sample.molecule[1].molecule_descriptionnull
experiment.sample.buffer.name50% dilution of protein buffer {10 mM KP, 50 mM NaCl, 10 mM DTT pH 6} with {milliQ-water pH 7} suspended RNA
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph6.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.name1:1 Mixture between Protein sex-lethal mutant (Sxl10GS) and RNA decaneucleotide UGU8
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_nameEMBL
experiment.contributor[0].affiliation[0].addressHeidelberg, Germany
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Heidelberg
experiment.contributor[0].affiliation[0].webpagehttps://www.embl.de/
experiment.contributor[0].contributor_namePo-chia
experiment.contributor[0].contributor_surnameChen
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2017-04-12
experiment.storage_temperature20.0
experiment.cell_temperature20.0
experiment.exposure_time0.5
experiment.number_of_frames10
experiment.wavelength0.09919
experiment.sample_detector_distance2.867
experiment.concentration_minnull
experiment.concentration_max1.0
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.031
experiment.s_max4.944
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].softwareEOM/GAJOE
fits[0].chi_square_value1.446
fits[0].p_value0.240677
fits[0].fit_residual_plotfit4columns1340_fitresiduals_img.png
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fits[0].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version4.5a
i0_calibration_standardnull
descriptionThis synchrotron session suffered from misalignment of the beamstop resulting in parasitic scattering at low angles. Note that the uploaded EOM ensemble is chosen as the 2:2-complex with one RNA monomer as fully bound by two Sxl10GS molecules in the canonical position from Protein data bankk (PDB) entry 1B7F.pdb. The second RNA monomer is placed in the canonical position bound to the free RRM2, resulting in three rigid bodies: RRM2+RNA, RRM1+RRM2+RNA, and RRM1.
experiment_descriptionSynchrotron SAXS data from solutions of a 1:1 mixture between Protein sex-lethal mutant (Sxl10GS) and RNA decaneucleotide UGU8 in 50% dilution of protein buffer (10 mM KP, 50 mM NaCl, 10 mM DTT), pH 6 were collected on the BM29 beam line at the ESRF storage ring (Grenoble, France) using a Pilatus 1M detector at a sample-detector distance of 2.9 m and at a wavelength of λ = 0.09919 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 1.00 mg/ml was measured at 20°C. 10 successive 0.500 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_unitarbitrary
experimental_mw24.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i077.67
pddf_i0_error0.08
guinier_i076.65
guinier_i0_error0.13
pddf_rg2.63
pddf_rg_error0.004
guinier_rg2.54
guinier_rg_error0.07
pddf_dmax8.88
pddf_dmax_errornull
porod_volume40.96
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first51
guinier_point_last92
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDD25_datloglog_img.png
symmetrynull
last_modified2020-08-28T15:27:59.704255+02:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDD25
statussuccess
started_at2026-08-11T14:35:46.695954+00:00
finished_at2026-08-11T14:35:55.791691+00:00
source_last_modified2020-08-28T15:27:59.704255+02:00
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查看完整 summary.json 原文
{
  "code": "SASDD25",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/nm",
  "project": {
    "title": "A General Small-Angle X-ray Scattering-Based Screening Protocol Validated for Protein-RNA Interactions.",
    "publication": {
      "title": "A General Small-Angle X-ray Scattering-Based Screening Protocol Validated for Protein-RNA Interactions.",
      "author_list": "Chen PC, Masiewicz P, Rybin V, Svergun D, Hennig J",
      "journal": "ACS Comb Sci",
      "doi": "10.1021/acscombsci.8b00007",
      "pmid": "29553252",
      "published_date": "2018 Apr 9"
    },
    "status": "released",
    "submitted_date": "2018-03-15",
    "released_date": "2018-03-21"
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      "country": "France",
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            "short_name": "EMBL",
            "address": "Heidelberg, Germany",
            "full_name": "European Molecular Biology Laboratory (EMBL) - Heidelberg",
            "webpage": "https://www.embl.de/"
          }
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        "contributor_name": "Po-chia",
        "contributor_surname": "Chen",
        "orcid": null
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  "last_modified": "2020-08-28T15:27:59.704255+02:00",
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}
查看完整 manifest.json 原文
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