SASDFS5

DNA-binding protein HU-alpha bound to 80 base-pair DNA at pH 7.5 with 300 mM NaCl

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2020-06-22T11:01:07.567483+02:00
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · DNA-binding protein HU-alpha bound to 80 base-pair DNA at pH 7.5 with 300 mM NaCl

浓度— – — 缓冲液 / pH10 mM Bis-Tris, 300 mM NaCl / 7.5
实验温度10.0 设备 / 束线Advanced Light Source (ALS) / 12.3.1 (SIBYLS)
波长0.103 nm曝光3.0 s × 300

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
80bp_DNA Forward
查看序列
AATGAGGTAACAACGAAAGCAGATGATAGCTGCTTATCAATTTGTTGCAAACAAGTAGCCGCGCCCAATGAGGTAACAAT
DNAEscherichia coli——–—monomer分子数 124.849 kDa
80bp_DNA Reverse
查看序列
TTACTCCATTGTTGCTTTCGTCTACTATCGACGAATAGTTAAACAACGTTTGTTCATCGGCGCGGGTTACTCCATTGTTA
DNAEscherichia coli——–—monomer分子数 124.612 kDa
DNA-binding protein HU-alpha
查看序列
MNKTQLIDVIAEKAELSKTQAKAALESTLAAITESLKEGDAVQLVGFGTFKVNHRAERTGRNPQTGKEIKIAAANVPAFVSGKALKDAVK
proteinEscherichia coliP0ACF01–90decamer分子数 109.535 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
1608[3]0.011985–0.3503 1/A含误差列缺失 00sasbdb/entries/s5/sasdfs5/source/SASDFS5.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)24.0—Å
i0Guinier101.312.42arbitrary
i0P(r)102.3—arbitrary
mwExperimental190.0—kDa
porod_volumePorod242.0—ų
rgGuinier6.50.2Å
rgP(r)6.97—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

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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10 mM Bis-Tris, 300 mM NaCl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2018-06-01储存 / 测量温度— / 10.0
曝光时间3.0帧数300
波长0.103样品-探测器距离1.5
光源X-ray synchrotron探测器Pilatus3 X 2M
机构 / 束线Advanced Light Source (ALS) / 12.3.1 (SIBYLS) · Berkeley, CA, USA
q 范围0.12 – 3.503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/s5/sasdfs5/source/SASDFS5.outdownloaded42498312fc82486e36f271b289359b10206212db078b0bb5722e2c0c61f741f1316db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(4 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:190 个字段值
字段路径原始值
codeSASDFS5
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleNucleoid remodeling during environmental adaptation is regulated by HU-dependent DNA bundling.
project.publication.titleNucleoid remodeling during environmental adaptation is regulated by HU-dependent DNA bundling.
project.publication.author_listRemesh SG, Verma SC, Chen JH, Ekman AA, Larabell CA, Adhya S, Hammel M
project.publication.journalNat Commun
project.publication.doi10.1038/s41467-020-16724-5
project.publication.pmid32518228
project.publication.published_date2020 Jun 9
project.statusreleased
project.submitted_date2019-04-26
project.released_date2020-04-21
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDFS5.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDFS5.dat
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sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDFS5.sascif
experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus3 X 2M
experiment.instrument.detector.resolution172.0
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_name80bp_DNA Forward
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceAATGAGGTAACAACGAAAGCAGATGATAGCTGCTTATCAATTTGTTGCAAACAAGTAGCCGCGCCCAATGAGGTAACAAT
experiment.sample.molecule[0].organismEscherichia coli
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_typeDNA
experiment.sample.molecule[0].uniprot_sequencenull
experiment.sample.molecule[0].mw24.849
experiment.sample.molecule[0].total_mw24.849
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.molecule[1].long_name80bp_DNA Reverse
experiment.sample.molecule[1].short_namenull
experiment.sample.molecule[1].sequenceTTACTCCATTGTTGCTTTCGTCTACTATCGACGAATAGTTAAACAACGTTTGTTCATCGGCGCGGGTTACTCCATTGTTA
experiment.sample.molecule[1].organismEscherichia coli
experiment.sample.molecule[1].uniprot_codenull
experiment.sample.molecule[1].uniprot_range_firstnull
experiment.sample.molecule[1].uniprot_range_lastnull
experiment.sample.molecule[1].oligomerizationmonomer
experiment.sample.molecule[1].molecular_typeDNA
experiment.sample.molecule[1].uniprot_sequencenull
experiment.sample.molecule[1].mw24.612
experiment.sample.molecule[1].total_mw24.612
experiment.sample.molecule[1].number_molecules1
experiment.sample.molecule[1].complex_stateFalse
experiment.sample.molecule[1].deuterationnull
experiment.sample.molecule[1].molecule_sourcebiological
experiment.sample.molecule[1].molecule_descriptionnull
experiment.sample.molecule[2].long_nameDNA-binding protein HU-alpha
experiment.sample.molecule[2].short_namenull
experiment.sample.molecule[2].sequenceMNKTQLIDVI AEKAELSKTQ AKAALESTLA AITESLKEGD AVQLVGFGTF KVNHRAERTG RNPQTGKEIK IAAANVPAFV SGKALKDAVK
experiment.sample.molecule[2].organismEscherichia coli
experiment.sample.molecule[2].uniprot_codeP0ACF0
experiment.sample.molecule[2].uniprot_range_first1
experiment.sample.molecule[2].uniprot_range_last90
experiment.sample.molecule[2].oligomerizationdecamer
experiment.sample.molecule[2].molecular_typeprotein
experiment.sample.molecule[2].uniprot_sequenceMNKTQLIDVIAEKAELSKTQAKAALESTLAAITESLKEGDAVQLVGFGTFKVNHRAERTG RNPQTGKEIKIAAANVPAFVSGKALKDAVK
experiment.sample.molecule[2].mw9.535
experiment.sample.molecule[2].total_mw95.35
experiment.sample.molecule[2].number_molecules10
experiment.sample.molecule[2].complex_stateFalse
experiment.sample.molecule[2].deuterationnull
experiment.sample.molecule[2].molecule_sourcebiological
experiment.sample.molecule[2].molecule_descriptionnull
experiment.sample.buffer.name10 mM Bis-Tris, 300 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.ph7.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameDNA-binding protein HU-alpha bound to 80 base-pair DNA at pH 7.5 with 300 mM NaCl
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_nameUCSF
experiment.contributor[0].affiliation[0].addressSan Francisco, CA, USA
experiment.contributor[0].affiliation[0].full_nameUniversity of California, San Francisco (UCSF)
experiment.contributor[0].affiliation[0].webpagehttps://www.ucsf.edu/
experiment.contributor[0].contributor_nameSoumya
experiment.contributor[0].contributor_surnameG Remesh
experiment.contributor[0].orcid
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2018-06-01
experiment.storage_temperaturenull
experiment.cell_temperature10.0
experiment.exposure_time3.0
experiment.number_of_frames300
experiment.wavelength0.103
experiment.sample_detector_distance1.5
experiment.concentration_minnull
experiment.concentration_maxnull
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.12
experiment.s_max3.503
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDFS5_fit1_model1_img.png
fits[0].models[0].softwareChimera
fits[0].models[0].pdb_link[]
fits[0].models[0].model_titlenull
fits[0].models[0].type_of_modelatomic
fits[0].models[0].software_versionnull
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fits[0].models[0].bead_radiusnull
fits[0].models[0].lognull
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fits[0].models[0].commentnull
fits[0].models[0].user293
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fits[0].softwareFoXS
fits[0].chi_square_value7.648103
fits[0].p_value0.0
fits[0].fit_residual_plotSASDFS5_fit1_fitresiduals_img.png
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fits[0].fit_lognull
fits[0].software_versionnull
fits[0].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of DNA-binding protein HU-alpha bound to 80 base-pair DNA in 10 mM Bis-Tris, 300 mM NaCl, pH 7.5 were collected on the 12.3.1 (SIBYLS) beam line at the Advanced Light Source (ALS) storage ring (Berkeley, CA, USA) using a Pilatus3 X 2M detector at a sample-detector distance of 1.5 m and at a wavelength of λ = 0.103 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). 300 successive 3 second frames were collected at 10°C. 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_mw190.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i0102.3
pddf_i0_errornull
guinier_i0101.31
guinier_i0_error2.42
pddf_rg6.97
pddf_rg_errornull
guinier_rg6.5
guinier_rg_error0.2
pddf_dmax24.0
pddf_dmax_errornull
porod_volume242.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first3
guinier_point_last14
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDFS5_datloglog_img.png
symmetrynull
last_modified2020-06-22T11:01:07.567483+02:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDFS5
statussuccess
started_at2026-08-11T16:52:37.462818+00:00
finished_at2026-08-11T16:52:51.111764+00:00
source_last_modified2020-06-22T11:01:07.567483+02:00
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查看完整 summary.json 原文
{
  "code": "SASDFS5",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Nucleoid remodeling during environmental adaptation is regulated by HU-dependent DNA bundling.",
    "publication": {
      "title": "Nucleoid remodeling during environmental adaptation is regulated by HU-dependent DNA bundling.",
      "author_list": "Remesh SG, Verma SC, Chen JH, Ekman AA, Larabell CA, Adhya S, Hammel M",
      "journal": "Nat Commun",
      "doi": "10.1038/s41467-020-16724-5",
      "pmid": "32518228",
      "published_date": "2020 Jun 9"
    },
    "status": "released",
    "submitted_date": "2019-04-26",
    "released_date": "2020-04-21"
  },
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    "sample": {
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        {
          "long_name": "80bp_DNA Forward",
          "short_name": null,
          "sequence": "AATGAGGTAACAACGAAAGCAGATGATAGCTGCTTATCAATTTGTTGCAAACAAGTAGCCGCGCCCAATGAGGTAACAAT",
          "organism": "Escherichia coli",
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            "address": "San Francisco, CA, USA",
            "full_name": "University of California, San Francisco (UCSF)",
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  "last_modified": "2020-06-22T11:01:07.567483+02:00",
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}
查看完整 manifest.json 原文
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