SASDCT6

12N12 nucleosome in 60% sucrose with ADP-BeF3

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2020-08-28T15:28:07.375857+02:00

12N12 nucleosome measured in 60% sucrose and ADP-BeF3. Due to contrast matching between the solvent and histone proteins (due to sucrose), the measured signal is dominated by the DNA component. The model was generated using 3D-DART and custom scripts written in Pymol. The percentage-weighting of each model in the ensemble ('XXXperc') is noted in the model key below: SASDCT6_fit1_model1 = 12N12_ADP_01_100perc

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · 12N12 nucleosome in 60% sucrose with ADP-BeF3

浓度— – 1.1 缓冲液 / pH10 mM Tris, 100 mM NaCl, 2 mM MgCl2, 0.1 mM EDTA, 1 mM DTT, 60% (w/v) sucrose, ADP-BeF3 (0.5 mM ADP, 4 mM NaF, 0.6 mM BeCl2) / 7.8
实验温度25.0 设备 / 束线Cornell High Energy Synchrotron Source (CHESS) / G1
波长0.1109 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
169 bp DNA (145 bp Widom 601, flanked by 12bp DNA)
查看序列
CTTTCAGCTGATATCGATGTATATATCTGACACGTGCCTGGAGACTAGGGAGTAATCCCCTTGGCGGTTAAAACGCGGGGGACAGCGCGTACGTGCGTTTAAGCGGTGCTAGAGCTGTCTACGACCAATTGAGCGGCCTCGGCACCGGGATCTTGATATCAGCTGAAAG
DNA———–—monomer分子数 152.468 kDa
Histone H2A type 1
查看序列
MSGRGKQGGKTRAKAKTRSSRAGLQFPVGRVHRLLRKGNYAERVGAGAPVYLAAVLEYLTAEILELAGNAARDNKKTRIIPRHLQLAVRNDEELNKLLGGVTIAQGGVLPNIQSVLLPKKTESAKSAKSK
proteinXenopus laevisP06897—–—monomer分子数 113.966 kDa
Histone H2B 1.1
查看序列
MPEPAKSAPAPKKGSKKAVTKTQKKDGKKRRKSRKESYAIYVYKVLKQVHPDTGISSKAMSIMNSFVNDVFERIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVTKYTSAK
proteinXenopus laevisP02281—–—monomer分子数 113.934 kDa
Histone H3.2
查看序列
MARTKQTARKSTGGKAPRKQLATKAARKSAPATGGVKKPHRYRPGTVALREIRRYQKSTELLIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEASEAYLVGLFEDTNLCAIHAKRVTIMPKDIQLARRIRGERA
proteinXenopus laevisP842331–136monomer分子数 115.388 kDa
Histone H4
查看序列
MSGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLKVFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
proteinXenopus laevisP62799—–—monomer分子数 111.367 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
1245[3]0.016–0.26 1/A含误差列缺失 022sasbdb/entries/t6/sasdct6/source/SASDCT6.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)14.0—Å
i0Guinier0.0216220.000176arbitrary
i0P(r)0.02220.00013arbitrary
mwExperimental105.0—kDa
rgGuinier4.8120.52Å
rgP(r)4.9370.026Å

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

拟合 1 · EOM/GAJOE 2.1 r7883

χ²:1.67CorMap p:0.0646单位:1/A
模型名称 / 类型软件对称性模型 MWPDB 声明来源文件
1—atomicCustom in-house —103.9—模型 图片
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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 Tris, 100 mM NaCl, 2 mM MgCl2, 0.1 mM EDTA, 1 mM DTT, 60% (w/v) sucrose, ADP-BeF3 (0.5 mM ADP, 4 mM NaF, 0.6 mM BeCl2)缓冲液浓度—
pH7.8添加剂—
缓冲液说明60% sucrose ADP-BeF3
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2015-10-24储存 / 测量温度25.0 / 25.0
曝光时间10.0帧数40
波长0.1109样品-探测器距离2.08
光源X-ray synchrotron探测器Pilatus 200K
机构 / 束线Cornell High Energy Synchrotron Source (CHESS) / G1 · Ithaca, NY, USA
q 范围0.16 – 2.6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/t6/sasdct6/source/SASDCT6.datdownloaded14966c79bac3633587f3f02c15d2c38a5cadaabd39bfb382db3afc3b2e58d6fe029e6下载查看原文件源站
full_entry_zipsasbdb/entries/t6/sasdct6/source/SASDCT6.zipdownloaded14815013a71e65821a05d57d9b168a1828346276b9ec77dc642c94f398f5574471901c下载查看原文件源站
pddfsasbdb/entries/t6/sasdct6/source/SASDCT6.outdownloaded273976ce02cc78f535808ed3e827ea84ec190ae77749e6d0f3946007d2d998d8c8e72下载查看原文件源站
sascifsasbdb/entries/t6/sasdct6/source/SASDCT6.sascifdownloaded6049f0c370df13d285deb97a908ee17adbb83e088b85a499936673be2f80fba5311e下载查看原文件源站
summarysasbdb/entries/t6/sasdct6/source/summary.jsondownloaded11403f9248f8b8735dff08a1bd1ecde13dd42e2ad0af75e34ed42a2b58fed0a188515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(5 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:224 个字段值
字段路径原始值
codeSASDCT6
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleThe ATPase motor of the Chd1 chromatin remodeler stimulates DNA unwrapping from the nucleosome.
project.publication.titleThe ATPase motor of the Chd1 chromatin remodeler stimulates DNA unwrapping from the nucleosome.
project.publication.author_listTokuda JM, Ren R, Levendosky RF, Tay RJ, Yan M, Pollack L, Bowman GD
project.publication.journalNucleic Acids Res
project.publication.doi10.1093/nar/gky206
project.publication.pmid29850894
project.publication.published_date2018 Jun 1
project.statusreleased
project.submitted_date2017-08-03
project.released_date2018-03-25
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDCT6.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDCT6.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDCT6_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDCT6_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDCT6_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDCT6_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDCT6.sascif
experiment.instrument.detector.typePilatus
experiment.instrument.detector.namePilatus 200K
experiment.instrument.detector.resolution172.0
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
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_name169 bp DNA (145 bp Widom 601, flanked by 12bp DNA)
experiment.sample.molecule[0].short_nameDNA
experiment.sample.molecule[0].sequenceCTTTCAGCTGATATCGATGTATATATCTGACACGTGCCTGGAGACTAGGGAGTAATCCCCTTGGCGGTTAAAACGCGGGGGACAGCGCGTACGTGCGTTTAAGCGGTGCTAGAGCTGTCTACGACCAATTGAGCGGCCTCGGCACCGGGATCTTGATATCAGCTGAAAG
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_typeDNA
experiment.sample.molecule[0].uniprot_sequencenull
experiment.sample.molecule[0].mw52.468
experiment.sample.molecule[0].total_mw52.468
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_nameHistone H2A type 1
experiment.sample.molecule[1].short_nameH2A
experiment.sample.molecule[1].sequenceMSGRGKQGGKTRAKAKTRSSRAGLQFPVGRVHRLLRKGNYAERVGAGAPVYLAAVLEYLT AEILELAGNAARDNKKTRIIPRHLQLAVRNDEELNKLLGGVTIAQGGVLPNIQSVLLPKK TESAKSAKSK
experiment.sample.molecule[1].organismXenopus laevis
experiment.sample.molecule[1].uniprot_codeP06897
experiment.sample.molecule[1].uniprot_range_firstnull
experiment.sample.molecule[1].uniprot_range_lastnull
experiment.sample.molecule[1].oligomerizationmonomer
experiment.sample.molecule[1].molecular_typeprotein
experiment.sample.molecule[1].uniprot_sequenceMSGRGKQGGKTRAKAKTRSSRAGLQFPVGRVHRLLRKGNYAERVGAGAPVYLAAVLEYLT AEILELAGNAARDNKKTRIIPRHLQLAVRNDEELNKLLGGVTIAQGGVLPNIQSVLLPKK TESAKSAKSK
experiment.sample.molecule[1].mw13.966
experiment.sample.molecule[1].total_mw13.966
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_nameHistone H2B 1.1
experiment.sample.molecule[2].short_nameH2B
experiment.sample.molecule[2].sequenceMPEPAKSAPAPKKGSKKAVTKTQKKDGKKRRKSRKESYAIYVYKVLKQVHPDTGISSKAM SIMNSFVNDVFERIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVT KYTSAK
experiment.sample.molecule[2].organismXenopus laevis
experiment.sample.molecule[2].uniprot_codeP02281
experiment.sample.molecule[2].uniprot_range_firstnull
experiment.sample.molecule[2].uniprot_range_lastnull
experiment.sample.molecule[2].oligomerizationmonomer
experiment.sample.molecule[2].molecular_typeprotein
experiment.sample.molecule[2].uniprot_sequenceMPEPAKSAPAPKKGSKKAVTKTQKKDGKKRRKSRKESYAIYVYKVLKQVHPDTGISSKAM SIMNSFVNDVFERIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVT KYTSAK
experiment.sample.molecule[2].mw13.934
experiment.sample.molecule[2].total_mw13.934
experiment.sample.molecule[2].number_molecules1
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.molecule[3].long_nameHistone H3.2
experiment.sample.molecule[3].short_nameH3
experiment.sample.molecule[3].sequenceMARTKQTARKSTGGKAPRKQLATKAARKSAPATGGVKKPHRYRPGTVALREIRRYQKSTE LLIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEASEAYLVGLFEDTNLCAIHAKRVTI MPKDIQLARRIRGERA
experiment.sample.molecule[3].organismXenopus laevis
experiment.sample.molecule[3].uniprot_codeP84233
experiment.sample.molecule[3].uniprot_range_first1
experiment.sample.molecule[3].uniprot_range_last136
experiment.sample.molecule[3].oligomerizationmonomer
experiment.sample.molecule[3].molecular_typeprotein
experiment.sample.molecule[3].uniprot_sequenceMARTKQTARKSTGGKAPRKQLATKAARKSAPATGGVKKPHRYRPGTVALREIRRYQKSTE LLIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEASEAYLVGLFEDTNLCAIHAKRVTI MPKDIQLARRIRGERA
experiment.sample.molecule[3].mw15.388
experiment.sample.molecule[3].total_mw15.388
experiment.sample.molecule[3].number_molecules1
experiment.sample.molecule[3].complex_stateFalse
experiment.sample.molecule[3].deuterationnull
experiment.sample.molecule[3].molecule_sourcebiological
experiment.sample.molecule[3].molecule_descriptionnull
experiment.sample.molecule[4].long_nameHistone H4
experiment.sample.molecule[4].short_nameH4
experiment.sample.molecule[4].sequenceMSGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLK VFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
experiment.sample.molecule[4].organismXenopus laevis
experiment.sample.molecule[4].uniprot_codeP62799
experiment.sample.molecule[4].uniprot_range_firstnull
experiment.sample.molecule[4].uniprot_range_lastnull
experiment.sample.molecule[4].oligomerizationmonomer
experiment.sample.molecule[4].molecular_typeprotein
experiment.sample.molecule[4].uniprot_sequenceMSGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLK VFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
experiment.sample.molecule[4].mw11.367
experiment.sample.molecule[4].total_mw11.367
experiment.sample.molecule[4].number_molecules1
experiment.sample.molecule[4].complex_stateFalse
experiment.sample.molecule[4].deuterationnull
experiment.sample.molecule[4].molecule_sourcebiological
experiment.sample.molecule[4].molecule_descriptionnull
experiment.sample.buffer.name10 mM Tris, 100 mM NaCl, 2 mM MgCl2, 0.1 mM EDTA, 1 mM DTT, 60% (w/v) sucrose, ADP-BeF3 (0.5 mM ADP, 4 mM NaF, 0.6 mM BeCl2)
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.comment60% sucrose ADP-BeF3
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.8
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.name12N12 nucleosome in 60% sucrose with ADP-BeF3
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_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_nameJoshua
experiment.contributor[0].contributor_surnameTokuda
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2015-10-24
experiment.storage_temperature25.0
experiment.cell_temperature25.0
experiment.exposure_time10.0
experiment.number_of_frames40
experiment.wavelength0.1109
experiment.sample_detector_distance2.08
experiment.concentration_minnull
experiment.concentration_max1.1
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.16
experiment.s_max2.6
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDCT6_fit1_model1_img.png
fits[0].models[0].softwareCustom in-house
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
fits[0].models[0].model_datahttps://www.sasbdb.org/media/pdb_file/SASDCT6_fit1_model1.pdb
fits[0].models[0].model_mw103.9
fits[0].models[0].bead_radius1.9
fits[0].models[0].lognull
fits[0].models[0].symmetrynull
fits[0].models[0].commentGenerated using 3D-DART and custom scripts written in Pymol. Percentage represents ensemble weight.
fits[0].models[0].user170
fits[0].fit_unit1/A
fits[0].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/SASDCT6_fit1_fixed_fit_img.png
fits[0].softwareEOM/GAJOE
fits[0].chi_square_value1.67
fits[0].p_value0.0646
fits[0].fit_residual_plotfit4columns1046_fitresiduals_img.png
fits[0].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDCT6_fit1.fit
fits[0].fit_lognull
fits[0].software_version2.1 r7883
fits[0].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versionVersion 5.0 (r4547)
i0_calibration_standardnull
description12N12 nucleosome measured in 60% sucrose and ADP-BeF3. Due to contrast matching between the solvent and histone proteins (due to sucrose), the measured signal is dominated by the DNA component. The model was generated using 3D-DART and custom scripts written in Pymol. The percentage-weighting of each model in the ensemble ('XXXperc') is noted in the model key below: SASDCT6_fit1_model1 = 12N12_ADP_01_100perc
experiment_descriptionSynchrotron SAXS data from solutions of 12N12 nucleosome in 60% sucrose with ADP-BeF3 in 10 mM Tris, 100 mM NaCl, 2 mM MgCl2, 0.1 mM EDTA, 1 mM DTT, 60% (w/v) sucrose, ADP-BeF3 (0.5 mM ADP, 4 mM NaF, 0.6 mM BeCl2), pH 7.8, were collected on the G1 beam line at the Cornell High Energy Synchrotron Source (Ithaca, NY, USA) using a Pilatus Pilatus 200K detector at a sample-detector distance of 2.1 m and at a wavelength of λ = 0.1109 nm (I(s) vs s, where s = 4πsinθ/λ and 2θ is the scattering angle). One solute concentration of 1.10 mg/ml was measured at 25°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 to produce the scattering profile displayed in this entry.
tags[]
intensity_unitarbitrary
experimental_mw105.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i00.0222
pddf_i0_error0.00013
guinier_i00.021622
guinier_i0_error0.000176
pddf_rg4.937
pddf_rg_error0.026
guinier_rg4.812
guinier_rg_error0.52
pddf_dmax14.0
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manifest.json:36 个字段值
字段路径原始值
codeSASDCT6
statussuccess
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查看完整 summary.json 原文
{
  "code": "SASDCT6",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "The ATPase motor of the Chd1 chromatin remodeler stimulates DNA unwrapping from the nucleosome.",
    "publication": {
      "title": "The ATPase motor of the Chd1 chromatin remodeler stimulates DNA unwrapping from the nucleosome.",
      "author_list": "Tokuda JM, Ren R, Levendosky RF, Tay RJ, Yan M, Pollack L, Bowman GD",
      "journal": "Nucleic Acids Res",
      "doi": "10.1093/nar/gky206",
      "pmid": "29850894",
      "published_date": "2018 Jun 1"
    },
    "status": "released",
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    "released_date": "2018-03-25"
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}
查看完整 manifest.json 原文
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