SASDEL3

The neutrophil cytosol factor 2 (p67phox) subunit of phagocyte NADPH oxidase

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Extrapolated to infinite dilution 最后更新:2020-08-28T15:27:52.342524+02:00
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · The neutrophil cytosol factor 2 (p67phox) subunit of phagocyte NADPH oxidase

浓度0.3 – 3.8 缓冲液 / pH20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol / 8.0
实验温度4.0 设备 / 束线LURE / D24
波长0.1488 nm曝光200.0 s × 8

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Neutrophil cytosol factor 2
查看序列
GPLGSPNSARMSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTILKNMTEAEKAFTRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYKILGLQFKLFACEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQKLYEPVVIPVGKLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPRPKTPEIFRALEGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVPCNYLEPVELRIHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPMPYTLKVHYKYTVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSMKDAWGQVKNYCLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEATQPEDLEFQEGDIILVLSKVNEEWLEGESKGKVGIFPKVFVEDSATTDLESTRREV
proteinHomo sapiensP198781–526monomer分子数 160.666 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
1175[3]0.014831–0.33741 1/A含误差列缺失 00sasbdb/entries/l3/sasdel3/source/SASDEL3.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)16.01.0Å
i0Guinier0.050.00061/cm
i0P(r)0.050880.00061/cm
mwExperimental62.4—kDa
mwGuinier I(0)60.46.0kDa
mwPorod75.3—kDa
porod_volumePorod113.0—ų
rgGuinier4.270.1Å
rgP(r)4.540.1Å

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 · BUNCH 08

χ²:1.304CorMap p:1e-06单位:1/A

p67phox in solution: Comparison of the experimental data (blue dots) with the calculated scattering pattern (red line) of the BUNCH model shown on the rightchi2=1.304. The ultimate adjustment shown here was performed using the program CRYSOL.

模型名称 / 类型软件对称性模型 MWPDB 声明来源文件
1—atomicCustom in-house —63.06—模型 图片

拟合 2 · EOM/GAJOE 2.1

χ²:0.828CorMap p:0.493356单位:1/A

The fitting to the experimental curve using EOM program. This good fit with our experimental intensities chi2=0.828) was obtained only when using the “compact” reconstructed linkers.

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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20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol缓冲液浓度—
pH8.0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2003-04-09储存 / 测量温度4.0 / 4.0
曝光时间200.0帧数8
波长0.1488样品-探测器距离1.378
光源X-ray synchrotron探测器Linear gas detector
机构 / 束线LURE / D24 · Orsay, France
q 范围0.148 – 3.374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/l3/sasdel3/source/SASDEL3.outdownloaded17987076b8a277d46cb46173f0533941e749e8594efea1a817e412d488c19d5509d46下载查看原文件源站
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summarysasbdb/entries/l3/sasdel3/source/summary.jsondownloaded96008c809402225ef87ba3e4de191a084373ee4ae6daca7696b3c7e9acde977e8336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:167 个字段值
字段路径原始值
codeSASDEL3
statusPublished
type_of_curveExtrapolated to infinite dilution
angular_unit1/A
project.titleQuantitative live-cell imaging and 3D modeling reveal critical functional features in the cytosolic complex of phagocyte NADPH oxidase.
project.publication.titleQuantitative live-cell imaging and 3D modeling reveal critical functional features in the cytosolic complex of phagocyte NADPH oxidase.
project.publication.author_listZiegler CS, Bouchab L, Tramier M, Durand D, Fieschi F, Dupré-Crochet S, Mérola F, Nüße O, Erard M
project.publication.journalJ Biol Chem
project.publication.doi10.1074/jbc.RA118.006864
project.publication.pmid30630949
project.publication.published_date2019 Jan 10
project.statusreleased
project.submitted_date2018-08-28
project.released_date2019-01-16
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDEL3.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDEL3.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDEL3_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDEL3.sascif
experiment.instrument.detector.typeCustom
experiment.instrument.detector.nameLinear gas detector
experiment.instrument.detector.resolution605.0
experiment.instrument.nameLURE
experiment.instrument.cityOrsay
experiment.instrument.countryFrance
experiment.instrument.beamline_nameD24
experiment.instrument.beam_geometrynull
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_nameNeutrophil cytosol factor 2
experiment.sample.molecule[0].short_namep67phox
experiment.sample.molecule[0].sequenceGPLGSPNSARMSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTIL KNMTEAEKAFTRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYK ILGLQFKLFACEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQK LYEPVVIPVGKLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPR PKTPEIFRALEGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVP CNYLEPVELRIHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPM PYTLKVHYKYTVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSM KDAWGQVKNYCLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEA TQPEDLEFQEGDIILVLSKVNEEWLEGESKGKVGIFPKVFVEDSATTDLESTRREV
experiment.sample.molecule[0].organismHomo sapiens
experiment.sample.molecule[0].uniprot_codeP19878
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last526
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTILKNMTEAEKAF TRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYKILGLQFKLFA CEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQKLYEPVVIPVG KLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPRPKTPEIFRAL EGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVPCNYLEPVELR IHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPMPYTLKVHYKY TVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSMKDAWGQVKNY CLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEATQPEDLEFQE GDIILVLSKVNEEWLEGECKGKVGIFPKVFVEDCATTDLESTRREV
experiment.sample.molecule[0].mw60.666
experiment.sample.molecule[0].total_mw60.666
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.name20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph8.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameThe neutrophil cytosol factor 2 (p67phox) subunit of phagocyte NADPH oxidase
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].addressParis, France
experiment.contributor[0].affiliation[0].full_nameI2BC-CNRS
experiment.contributor[0].affiliation[0].webpagehttp://www.i2bc.paris-saclay.fr
experiment.contributor[0].contributor_nameDominique
experiment.contributor[0].contributor_surnameDURAND
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2003-04-09
experiment.storage_temperature4.0
experiment.cell_temperature4.0
experiment.exposure_time200.0
experiment.number_of_frames8
experiment.wavelength0.1488
experiment.sample_detector_distance1.378
experiment.concentration_min0.3
experiment.concentration_max3.8
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.148
experiment.s_max3.374
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDEL3_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
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fits[0].models[0].model_mw63.06
fits[0].models[0].bead_radiusnull
fits[0].models[0].lognull
fits[0].models[0].symmetrynull
fits[0].models[0].commentnull
fits[0].models[0].user262
fits[0].fit_unit1/A
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fits[0].softwareBUNCH
fits[0].chi_square_value1.304
fits[0].p_value1e-06
fits[0].fit_residual_plotfit4columns1678_fitresiduals_img.png
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fits[0].fit_loghttps://www.sasbdb.org/media/fitting_files/log_files/p67_Model00.log
fits[0].software_version08
fits[0].descriptionp67phox in solution: Comparison of the experimental data (blue dots) with the calculated scattering pattern (red line) of the BUNCH model shown on the rightchi2=1.304. The ultimate adjustment shown here was performed using the program CRYSOL.
fits[1].models[]
fits[1].fit_unit1/A
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fits[1].softwareEOM/GAJOE
fits[1].chi_square_value0.828
fits[1].p_value0.493356
fits[1].fit_residual_plotfit4columns1679_fitresiduals_img.png
fits[1].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDEL3_fit2.fit
fits[1].fit_lognull
fits[1].software_version2.1
fits[1].descriptionThe fitting to the experimental curve using EOM program. This good fit with our experimental intensities chi2=0.828) was obtained only when using the “compact” reconstructed linkers.
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of the p67phox subunit of phagocyte NADPH oxidase in 20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol, pH 8 were collected on the D24 beam line at the LURE storage ring (Orsay, France) using a linear gas home-made detector at a sample-detector distance of 1.4 m and at a wavelength of λ = 0.1488 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Samples were studied at different concentrations ranging from 0.3 to 3.8 mg/ml measured at 4°C. Eight successive 200 second frames were collected. SAXS data were normalized to the intensity of the incident beam, averaged and background subtracted using the program package PRIMUS. Intensities were put on an absolute scale (cm-1) using water scattering. The final pattern used for fitting was obtained by extrapolating to infinite dilution of the set of curves recorded at the different concentrations. Molecular mass was obtained using the bayesian inference approach proposed in PRIMUS/qt, which combines four concentration independent MM estimators: M=62.4 kDa within the credibility interval [60.2-67.9].
tags[]
intensity_unit1/cm
experimental_mw62.4
experimental_mw_errornull
guinier_i0_mw60.4
guinier_i0_mw_error6.0
porod_mw75.3
porod_mw_errornull
pddf_i00.05088
pddf_i0_error0.0006
guinier_i00.05
guinier_i0_error0.0006
pddf_rg4.54
pddf_rg_error0.1
guinier_rg4.27
guinier_rg_error0.1
pddf_dmax16.0
pddf_dmax_error1.0
porod_volume113.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last8
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDEL3_datloglog_img.png
symmetrynull
last_modified2020-08-28T15:27:52.342524+02:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDEL3
statussuccess
started_at2026-08-11T14:02:41.380130+00:00
finished_at2026-08-11T14:02:49.689847+00:00
source_last_modified2020-08-28T15:27:52.342524+02:00
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查看完整 summary.json 原文
{
  "code": "SASDEL3",
  "status": "Published",
  "type_of_curve": "Extrapolated to infinite dilution",
  "angular_unit": "1/A",
  "project": {
    "title": "Quantitative live-cell imaging and 3D modeling reveal critical functional features in the cytosolic complex of phagocyte NADPH oxidase.",
    "publication": {
      "title": "Quantitative live-cell imaging and 3D modeling reveal critical functional features in the cytosolic complex of phagocyte NADPH oxidase.",
      "author_list": "Ziegler CS, Bouchab L, Tramier M, Durand D, Fieschi F, Dupré-Crochet S, Mérola F, Nüße O, Erard M",
      "journal": "J Biol Chem",
      "doi": "10.1074/jbc.RA118.006864",
      "pmid": "30630949",
      "published_date": "2019 Jan 10"
    },
    "status": "released",
    "submitted_date": "2018-08-28",
    "released_date": "2019-01-16"
  },
  "pddf_data": "https://www.sasbdb.org/media/p_of_R_files/SASDEL3.out",
  "intensities_data": "https://www.sasbdb.org/media/intensities_files/SASDEL3.dat",
  "intensities_log_plot": "https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_dat_img.png",
  "intensities_kratky_plot": "https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_kratky_img.png",
  "pddf_plot": "https://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDEL3_pofr_img.png",
  "intensities_guinier_plot": "https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDEL3_guinier_img.png",
  "sascif_data": "https://www.sasbdb.org/media/sascif/sascif_files/SASDEL3.sascif",
  "experiment": {
    "instrument": {
      "detector": {
        "type": "Custom",
        "name": "Linear gas detector",
        "resolution": 605.0
      },
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      "city": "Orsay",
      "country": "France",
      "beamline_name": "D24",
      "beam_geometry": null,
      "type_of_source": "X-ray synchrotron",
      "point_source": null,
      "line_collimation": null,
      "sample_path_length": null,
      "line_collimation_slitlength": null,
      "line_collimation_integrationwidth": null,
      "xray_energy": null,
      "beam_profile_ah": null,
      "beam_profile_al": null
    },
    "sample": {
      "molecule": [
        {
          "long_name": "Neutrophil cytosol factor 2",
          "short_name": "p67phox",
          "sequence": "GPLGSPNSARMSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTIL\r\nKNMTEAEKAFTRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYK\r\nILGLQFKLFACEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQK\r\nLYEPVVIPVGKLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPR\r\nPKTPEIFRALEGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVP\r\nCNYLEPVELRIHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPM\r\nPYTLKVHYKYTVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSM\r\nKDAWGQVKNYCLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEA\r\nTQPEDLEFQEGDIILVLSKVNEEWLEGESKGKVGIFPKVFVEDSATTDLESTRREV",
          "organism": "Homo sapiens",
          "uniprot_code": "P19878",
          "uniprot_range_first": 1,
          "uniprot_range_last": 526,
          "oligomerization": "monomer",
          "molecular_type": "protein",
          "uniprot_sequence": "MSLVEAISLWNEGVLAADKKDWKGALDAFSAVQDPHSRICFNIGCMYTILKNMTEAEKAF\nTRSINRDKHLAVAYFQRGMLYYQTEKYDLAIKDLKEALIQLRGNQLIDYKILGLQFKLFA\nCEVLYNIAFMYAKKEEWKKAEEQLALATSMKSEPRHSKIDKAMECVWKQKLYEPVVIPVG\nKLFRPNERQVAQLAKKDYLGKATVVASVVDQDSFSGFAPLQPQAAEPPPRPKTPEIFRAL\nEGEAHRVLFGFVPETKEELQVMPGNIVFVLKKGNDNWATVMFNGQKGLVPCNYLEPVELR\nIHPQQQPQEESSPQSDIPAPPSSKAPGRPQLSPGQKQKEEPKEVKLSVPMPYTLKVHYKY\nTVVMKTQPGLPYSQVRDMVSKKLELRLEHTKLSYRPRDSNELVPLSEDSMKDAWGQVKNY\nCLTLWCENTVGDQGFPDEPKESEKADANNQTTEPQLKKGSQVEALFSYEATQPEDLEFQE\nGDIILVLSKVNEEWLEGECKGKVGIFPKVFVEDCATTDLESTRREV",
          "mw": 60.666,
          "total_mw": 60.666,
          "number_molecules": 1,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
      ],
      "buffer": {
        "name": "20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol",
        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 8.0,
        "deuteration": null
      },
      "purity_method": null,
      "name": "The neutrophil cytosol factor 2 (p67phox) subunit of phagocyte NADPH oxidase",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": null,
            "address": "Paris, France",
            "full_name": "I2BC-CNRS",
            "webpage": "http://www.i2bc.paris-saclay.fr"
          }
        ],
        "contributor_name": "Dominique",
        "contributor_surname": "DURAND",
        "orcid": null
      }
    ],
    "concentration_method": null,
    "concentration_unit": null,
    "date": "2003-04-09",
    "storage_temperature": 4.0,
    "cell_temperature": 4.0,
    "exposure_time": 200.0,
    "number_of_frames": 8,
    "wavelength": 0.1488,
    "sample_detector_distance": 1.378,
    "concentration_min": 0.3,
    "concentration_max": 3.8,
    "sample_volume": null,
    "flow_rate": null,
    "s_min": 0.148,
    "s_max": 3.374,
    "total_exposure_time": null,
    "seccolumn": null
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      "models": [
        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDEL3_fit1_model1_img.png",
          "software": "Custom in-house",
          "pdb_link": [],
          "model_title": null,
          "type_of_model": "atomic",
          "software_version": null,
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDEL3_fit1_model1.pdb",
          "model_mw": 63.06,
          "bead_radius": null,
          "log": null,
          "symmetry": null,
          "comment": null,
          "user": 262
        }
      ],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDEL3_fit1_fixed_fit_img.png",
      "software": "BUNCH",
      "chi_square_value": 1.304,
      "p_value": 1e-06,
      "fit_residual_plot": "fit4columns1678_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDEL3_fit1.fit",
      "fit_log": "https://www.sasbdb.org/media/fitting_files/log_files/p67_Model00.log",
      "software_version": "08",
      "description": "p67phox in solution: \r\nComparison of the experimental data (blue dots) with the calculated scattering pattern (red line) of the BUNCH model shown on the rightchi2=1.304. The ultimate adjustment shown here was performed using the program CRYSOL."
    },
    {
      "models": [],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDEL3_fit2_fixed_fit_img.png",
      "software": "EOM/GAJOE",
      "chi_square_value": 0.828,
      "p_value": 0.493356,
      "fit_residual_plot": "fit4columns1679_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDEL3_fit2.fit",
      "fit_log": null,
      "software_version": "2.1",
      "description": "The fitting to the experimental curve using EOM program. This good fit with our experimental intensities chi2=0.828) was obtained only when using the “compact” reconstructed linkers."
    }
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  "pddf_software": "ATSAS GNOM",
  "pddf_software_version": "5.0",
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  "description": null,
  "experiment_description": "Synchrotron SAXS data from solutions of the p67phox subunit of phagocyte NADPH oxidase in 20 mM HEPES, 50 mM NaCl, 1 mM EDTA, 2 mM DTT, 5% glycerol, pH 8 were collected on the D24 beam line at the LURE storage ring (Orsay, France) using a linear gas home-made detector at a sample-detector distance of 1.4 m and at a wavelength of λ = 0.1488 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Samples were studied at different concentrations ranging from 0.3 to 3.8 mg/ml measured at 4°C. Eight successive 200 second frames were collected. SAXS data were normalized to the intensity of the incident beam, averaged and background subtracted using the program package PRIMUS. Intensities were put on an absolute scale (cm-1) using water scattering. The final pattern used for fitting was obtained by extrapolating to infinite dilution of the set of curves recorded at the different concentrations. Molecular mass was obtained using the bayesian inference approach proposed in PRIMUS/qt, which combines four concentration independent MM estimators: M=62.4 kDa within the credibility interval [60.2-67.9].",
  "tags": [],
  "intensity_unit": "1/cm",
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  "experimental_mw_error": null,
  "guinier_i0_mw": 60.4,
  "guinier_i0_mw_error": 6.0,
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  "pddf_i0_error": 0.0006,
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  "guinier_i0_error": 0.0006,
  "pddf_rg": 4.54,
  "pddf_rg_error": 0.1,
  "guinier_rg": 4.27,
  "guinier_rg_error": 0.1,
  "pddf_dmax": 16.0,
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  "porod_volume": 113.0,
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  "estimated_volume": null,
  "estimated_volume_error": null,
  "guinier_point_first": 1,
  "guinier_point_last": 8,
  "pddf_point_first": null,
  "pddf_point_last": null,
  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDEL3_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2020-08-28T15:27:52.342524+02:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
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  "finished_at": "2026-08-11T14:02:49.689847+00:00",
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