SASDFM7

Complex with 1H histone chaperone Asf1, histones H3 and H4, acetylatransferase Rtt109, 2H histone chaperone Vps75 (1-225aa) in 42% v/v D2O

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2022-08-15T14:51:04.900446+02:00
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Complex with 1H histone chaperone Asf1, histones H3 and H4, acetylatransferase Rtt109, 2H histone chaperone Vps75 (1-225aa) in 42% v/v D2O

浓度— – 4.9 缓冲液 / pH50 mM citrate, 150 mM NaCl, 5 mM BME, 42% D2O / 6.5
实验温度25.1 设备 / 束线Institut Laue-Langevin (ILL) / D22
波长0.6 nm曝光3600.0 s × 1

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Vacuolar protein sorting-associated protein 75 (1-225 aa)
查看序列
MMSDQENENEHAKAFLGLAKCEEEVDAIEREVELYRLNKMKPVYEKRDAYIDEIAEFWKIVLSQHVSFANYIRASDFKYIDTIDKIKVEWLALESEMYDTRDFSITFHFHGIEGDFKEQQVTKVFQIKKGKDDQEDGILTSEPVPIEWPQSYDSINPDLIKDKRSPEGKKKYRQGMKTIFGWFRWTGLKPGKEFPHGDSLASLFSEEIYPFCVKYYAEAQRDLED
proteinSaccharomyces cerevisiaeP538531–225dimer分子数 226.554 kDa
Histone acetyltransferase RTT109
查看序列
MSLNDFLSSVLPVSEQFEYLSLQSIPLETHAVVTPNKDDKRVPKSTIKTQHFFSLFHQGKVFFSLEVYVYVTLWDEADAERLIFVSKADTNGYCNTRVSVRDITKIILEFILSIDPNYYLQKVKPAIRSYKKISPELISAASTPARTLRILARRLKQSGSTVLKEIESPRFQQDLYLSFTCPREILTKICLFTRPASQYLFPDSSKNSKKHILNGEELMKWWGFILDRLLIECFQNDTQAKLRIPGEDPARVRSYLRGMKYPLWQVGDIFTSKENSLAVYNIPLFPDDPKARFIHQLAEEDRLLKVSLSSFWIELQERQEFKLSVTSSVMGISGYSLATPSLFPSSADVIVPKSRKQFRAIKKYITGEEYDTEEGAIEAFTNIRDFLLLRMATNLQSLTGKREHRERNQPVPASNINTLAITMLKPRKKAKALPKT
proteinSaccharomyces cerevisiaeQ077941–436monomer分子数 150.095 kDa
Histone chaperone ASF1
查看序列
MSIVSLLGIKVLNNPAKFTDPYEFEITFECLESLKHDLEWKLTYVGSSRSLDHDQELDSILVGPVPVGVNKFVFSADPPSAELIPASELVSVTVILLSCSYDGREFVRVGYYVNNEYDEEELRENPPAKVQVDHIVRNILAEKPRVTRFNIVWDNENEGDLYPPEQPGV
protein—P324471–169monomer分子数 119.125 kDa
Histone H4
查看序列
MSGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLKVFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
proteinXenopus laevisP627991–103monomer分子数 111.367 kDa
Histone H3 full-length
查看序列
MARTKQTARKSTGGKAPRKQLATKAARKSAPSTGGVKKPHRYRPGTVALREIRRYQKSTELLIRKLPFQRLVREIAQDFKTDLRFQSAAIGALQEASEAYLVGLFEDTNLCAIHAKRVTIMPKDIQLARRIRGERA
proteinXenopus laevisQ6PI791–136monomer分子数 115.328 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
1110[3]0.0121709–0.240518 1/A含误差列缺失 010sasbdb/entries/m7/sasdfm7/source/SASDFM7.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)9.0—Å
i0Guinier0.146580.0014arbitrary
i0P(r)0.1471—arbitrary
mwExperimental149.0—kDa
rgGuinier2.7410.04Å
rgP(r)2.78—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

拟合 1 · CRYSON

χ²:0.286CorMap p:0.184911单位:1/A

Fit to the original X-ray structure (PDB 3q66)

模型名称 / 类型软件对称性模型 MWPDB 声明来源文件
1—atomicPDB (Protein Data Bank) —103.03Q66模型 图片

拟合 2 · CRYSON

χ²:0.244CorMap p:0.184911单位:1/A

Fit ot the selected MD model based on PDB 3q66.

模型名称 / 类型软件对称性模型 MWPDB 声明来源文件
1—atomicGROMACS —101.13Q66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50 mM citrate, 150 mM NaCl, 5 mM BME, 42% D2O缓冲液浓度—
pH6.5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2016-11-14储存 / 测量温度— / 25.1
曝光时间3600.0帧数1
波长0.6样品-探测器距离4.0
光源neutron source探测器Reuter-Stokes 3He
机构 / 束线Institut Laue-Langevin (ILL) / D22 · Grenoble, France
q 范围0.122 – 2.405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/m7/sasdfm7/source/SASDFM7.datdownloaded533147c7976e529cac2d8ae6d18d0b55115f543956490ef16914b3cacfbe9880d9c2下载查看原文件源站
full_entry_zipsasbdb/entries/m7/sasdfm7/source/SASDFM7.zipdownloaded54966431ed88f560ccaa7056f12019ed46aa1b57687404881a46fb83942936f61e1227下载查看原文件源站
pddfsasbdb/entries/m7/sasdfm7/source/SASDFM7.outdownloaded123532cc98ee7c5f5bfbef8e1ad9735c068434c336ad98a704b3c944d9d32815a4126下载查看原文件源站
sascifsasbdb/entries/m7/sasdfm7/source/SASDFM7.sascifdownloaded2262799900d28294931755c7988eee76f4348802b432ac9284477bbeb759cb74fa7d11e下载查看原文件源站
summarysasbdb/entries/m7/sasdfm7/source/summary.jsondownloaded13490c5e5184a40ad6c704269c1b9386894f486f2227a6dfd614ae1705355bf8e3e79下载查看原文件源站
curve:来源记录
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  "status": "downloaded",
  "url": "https://www.sasbdb.org/media/intensities_files/SASDFM7.dat"
}
full_entry_zip:来源记录与 ZIP 内部目录(6 项)
{
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  "status": "downloaded",
  "url": "https://www.sasbdb.org/media/zip_directories/SASDFM7.zip",
  "zip_member_count": 6,
  "zip_members": [
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      "name": "SASDFM7/pddf/SASDFM7.out",
      "size": 12353
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    {
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      "name": "SASDFM7/SASDFM7_fit1.fit",
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      "size": 1299726
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}
pddf:来源记录
{
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  "role": "pddf",
  "sha256": "2cc98ee7c5f5bfbef8e1ad9735c068434c336ad98a704b3c944d9d32815a4126",
  "size": 12353,
  "status": "downloaded",
  "url": "https://www.sasbdb.org/media/p_of_R_files/SASDFM7.out"
}
sascif:来源记录
{
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  "role": "sascif",
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  "size": 2262799,
  "status": "downloaded",
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summary:来源记录
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  "size": 13490,
  "status": "downloaded",
  "url": "https://www.sasbdb.org/rest-api/entry/summary/SASDFM7/"
}

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:253 个字段值
字段路径原始值
codeSASDFM7
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleHistone chaperone exploits intrinsic disorder to switch acetylation specificity (Asf1-H3:H4-Rtt109-Vps75 protein complex, data for docking block selections)
project.publication.titleHistone chaperone exploits intrinsic disorder to switch acetylation specificity (Asf1-H3:H4-Rtt109-Vps75 protein complex, data for docking block selections)
project.publication.author_listDanilenko N, Lercher L, Kirkpatrick J, Gabel F, Codutti L, Carlomagno T
project.publication.journalNat Commun
project.publication.doinull
project.publication.pmidnull
project.publication.published_date2019 Aug 6
project.statusreleased
project.submitted_date2019-06-17
project.released_date2019-07-10
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDFM7.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDFM7.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFM7_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFM7_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDFM7_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFM7_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDFM7.sascif
experiment.instrument.detector.type128 linear sensitive multidetector
experiment.instrument.detector.nameReuter-Stokes 3He
experiment.instrument.detector.resolution0.8
experiment.instrument.nameInstitut Laue-Langevin (ILL)
experiment.instrument.cityGrenoble
experiment.instrument.countryFrance
experiment.instrument.beamline_nameD22
experiment.instrument.beam_geometrynull
experiment.instrument.type_of_sourceneutron source
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_nameVacuolar protein sorting-associated protein 75 (1-225 aa)
experiment.sample.molecule[0].short_nameVps75 1-225
experiment.sample.molecule[0].sequenceMMSDQENENEHAKAFLGLAKCEEEVDAIEREVELYRLNKMKPVYEKRDAYIDEIAEFWKI VLSQHVSFANYIRASDFKYIDTIDKIKVEWLALESEMYDTRDFSITFHFHGIEGDFKEQQ VTKVFQIKKGKDDQEDGILTSEPVPIEWPQSYDSINPDLIKDKRSPEGKKKYRQGMKTIF GWFRWTGLKPGKEFPHGDSLASLFSEEIYPFCVKYYAEAQRDLED
experiment.sample.molecule[0].organismSaccharomyces cerevisiae
experiment.sample.molecule[0].uniprot_codeP53853
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last225
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMMSDQENENEHAKAFLGLAKCEEEVDAIEREVELYRLNKMKPVYEKRDAYIDEIAEFWKI VLSQHVSFANYIRASDFKYIDTIDKIKVEWLALESEMYDTRDFSITFHFHGIEGDFKEQQ VTKVFQIKKGKDDQEDGILTSEPVPIEWPQSYDSINPDLIKDKRSPEGKKKYRQGMKTIF GWFRWTGLKPGKEFPHGDSLASLFSEEIYPFCVKYYAEAQRDLEDEEGESGLSADGDSED DDGSLGEVDLPLSDEEPSSKKRKV
experiment.sample.molecule[0].mw26.554
experiment.sample.molecule[0].total_mw53.108
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_nameHistone acetyltransferase RTT109
experiment.sample.molecule[1].short_nameRtt109
experiment.sample.molecule[1].sequenceMSLNDFLSSVLPVSEQFEYLSLQSIPLETHAVVTPNKDDKRVPKSTIKTQHFFSLFHQGK VFFSLEVYVYVTLWDEADAERLIFVSKADTNGYCNTRVSVRDITKIILEFILSIDPNYYL QKVKPAIRSYKKISPELISAASTPARTLRILARRLKQSGSTVLKEIESPRFQQDLYLSFT CPREILTKICLFTRPASQYLFPDSSKNSKKHILNGEELMKWWGFILDRLLIECFQNDTQA KLRIPGEDPARVRSYLRGMKYPLWQVGDIFTSKENSLAVYNIPLFPDDPKARFIHQLAEE DRLLKVSLSSFWIELQERQEFKLSVTSSVMGISGYSLATPSLFPSSADVIVPKSRKQFRA IKKYITGEEYDTEEGAIEAFTNIRDFLLLRMATNLQSLTGKREHRERNQPVPASNINTLA ITMLKPRKKAKALPKT
experiment.sample.molecule[1].organismSaccharomyces cerevisiae
experiment.sample.molecule[1].uniprot_codeQ07794
experiment.sample.molecule[1].uniprot_range_first1
experiment.sample.molecule[1].uniprot_range_last436
experiment.sample.molecule[1].oligomerizationmonomer
experiment.sample.molecule[1].molecular_typeprotein
experiment.sample.molecule[1].uniprot_sequenceMSLNDFLSSVLPVSEQFEYLSLQSIPLETHAVVTPNKDDKRVPKSTIKTQHFFSLFHQGK VFFSLEVYVYVTLWDEADAERLIFVSKADTNGYCNTRVSVRDITKIILEFILSIDPNYYL QKVKPAIRSYKKISPELISAASTPARTLRILARRLKQSGSTVLKEIESPRFQQDLYLSFT CPREILTKICLFTRPASQYLFPDSSKNSKKHILNGEELMKWWGFILDRLLIECFQNDTQA KLRIPGEDPARVRSYLRGMKYPLWQVGDIFTSKENSLAVYNIPLFPDDPKARFIHQLAEE DRLLKVSLSSFWIELQERQEFKLSVTSSVMGISGYSLATPSLFPSSADVIVPKSRKQFRA IKKYITGEEYDTEEGAIEAFTNIRDFLLLRMATNLQSLTGKREHRERNQPVPASNINTLA ITMLKPRKKAKALPKT
experiment.sample.molecule[1].mw50.095
experiment.sample.molecule[1].total_mw50.095
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 chaperone ASF1
experiment.sample.molecule[2].short_nameAsf1
experiment.sample.molecule[2].sequenceMSIVSLLGIKVLNNPAKFTDPYEFEITFECLESLKHDLEWKLTYVGSSRSLDHDQELDSI LVGPVPVGVNKFVFSADPPSAELIPASELVSVTVILLSCSYDGREFVRVGYYVNNEYDEE ELRENPPAKVQVDHIVRNILAEKPRVTRFNIVWDNENEGDLYPPEQPGV
experiment.sample.molecule[2].organismnull
experiment.sample.molecule[2].uniprot_codeP32447
experiment.sample.molecule[2].uniprot_range_first1
experiment.sample.molecule[2].uniprot_range_last169
experiment.sample.molecule[2].oligomerizationmonomer
experiment.sample.molecule[2].molecular_typeprotein
experiment.sample.molecule[2].uniprot_sequenceMSIVSLLGIKVLNNPAKFTDPYEFEITFECLESLKHDLEWKLTYVGSSRSLDHDQELDSI LVGPVPVGVNKFVFSADPPSAELIPASELVSVTVILLSCSYDGREFVRVGYYVNNEYDEE ELRENPPAKVQVDHIVRNILAEKPRVTRFNIVWDNENEGDLYPPEQPGVDDEEEEDDEEE DDDEDDEDDEDDDQEDGEGEAEEAAEEEEEEEEKTEDNETNLEEEEEDIENSDGDEEEGE EEVGSVDKNEDGNDKKRRKIEGGSTDIESTPKDAARSTN
experiment.sample.molecule[2].mw19.125
experiment.sample.molecule[2].total_mw19.125
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 H4
experiment.sample.molecule[3].short_nameH4
experiment.sample.molecule[3].sequenceMSGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLK VFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
experiment.sample.molecule[3].organismXenopus laevis
experiment.sample.molecule[3].uniprot_codeP62799
experiment.sample.molecule[3].uniprot_range_first1
experiment.sample.molecule[3].uniprot_range_last103
experiment.sample.molecule[3].oligomerizationmonomer
experiment.sample.molecule[3].molecular_typeprotein
experiment.sample.molecule[3].uniprot_sequenceMSGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLK VFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
experiment.sample.molecule[3].mw11.367
experiment.sample.molecule[3].total_mw11.367
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 H3 full-length
experiment.sample.molecule[4].short_nameH3 FL
experiment.sample.molecule[4].sequenceMARTKQTARKSTGGKAPRKQLATKAARKSAPSTGGVKKPHRYRPGTVALR EIRRYQKSTELLIRKLPFQRLVREIAQDFKTDLRFQSAAIGALQEASEAY LVGLFEDTNLCAIHAKRVTIMPKDIQLARRIRGERA
experiment.sample.molecule[4].organismXenopus laevis
experiment.sample.molecule[4].uniprot_codeQ6PI79
experiment.sample.molecule[4].uniprot_range_first1
experiment.sample.molecule[4].uniprot_range_last136
experiment.sample.molecule[4].oligomerizationmonomer
experiment.sample.molecule[4].molecular_typeprotein
experiment.sample.molecule[4].uniprot_sequenceMARTKQTARKSTGGKAPRKQLATKAARKSAPSTGGVKKPHRYRPGTVALREIRRYQKSTE LLIRKLPFQRLVREIAQDFKTDLRFQSAAIGALQEASEAYLVGLFEDTNLCAIHAKRVTI MPKDIQLARRIRGERA
experiment.sample.molecule[4].mw15.328
experiment.sample.molecule[4].total_mw15.328
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.name50 mM citrate, 150 mM NaCl, 5 mM BME, 42% D2O
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph6.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameComplex with 1H histone chaperone Asf1, histones H3 and H4, acetylatransferase Rtt109, 2H histone chaperone Vps75 (1-225aa) in 42% v/v D2O
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].addressGermany
experiment.contributor[0].affiliation[0].full_nameLeibniz University of Hannover
experiment.contributor[0].affiliation[0].webpagehttps://www.uni-hannover.de
experiment.contributor[0].contributor_nameNataliya
experiment.contributor[0].contributor_surnameDanilenko
experiment.contributor[0].orcidhttps://orcid.org/0000-0003-4885-5051
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2016-11-14
experiment.storage_temperaturenull
experiment.cell_temperature25.1
experiment.exposure_time3600.0
experiment.number_of_frames1
experiment.wavelength0.6
experiment.sample_detector_distance4.0
experiment.concentration_minnull
experiment.concentration_max4.9
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.122
experiment.s_max2.405
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDFM7_fit1_model1_img.png
fits[0].models[0].softwarePDB (Protein Data Bank)
fits[0].models[0].pdb_link[0].pdb_code3q66
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manifest.json:36 个字段值
字段路径原始值
codeSASDFM7
statussuccess
started_at2026-08-11T15:33:37.736376+00:00
finished_at2026-08-11T15:33:53.060577+00:00
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查看完整 summary.json 原文
{
  "code": "SASDFM7",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Histone chaperone exploits intrinsic disorder to switch acetylation specificity (Asf1-H3:H4-Rtt109-Vps75 protein complex, data for docking block selections)",
    "publication": {
      "title": "Histone chaperone exploits intrinsic disorder to switch acetylation specificity (Asf1-H3:H4-Rtt109-Vps75 protein complex, data for docking block selections)",
      "author_list": "Danilenko N, Lercher L, Kirkpatrick J, Gabel F, Codutti L, Carlomagno T",
      "journal": "Nat Commun",
      "doi": null,
      "pmid": null,
      "published_date": "2019 Aug 6"
    },
    "status": "released",
    "submitted_date": "2019-06-17",
    "released_date": "2019-07-10"
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查看完整 manifest.json 原文
{
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