SASDDR4

LIM/homeobox protein Lhx4 LIM domains fused to the LIM interaction domain (LID) R282G mutant of Insulin gene enhancer protein ISL-2

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Extrapolated to infinite dilution 最后更新:2019-12-06T13:07:15.624532+01:00

The protein anaysed is a fusion of two interacting partners: the LIM domains of Lhx4 and the LID of Isl2, with a point mutation within the Isl2-LID (R282G). The ab initio bead models presented in this entry include: 1) The best-fit individual reconstruction (top) and; 2) The spatially aligned and volume/bead occupancy-corrected averaged representation of the protein in solution (bottom) calculated from twenty individual reconstructions (NSD = 0.67; resolution estimate = 2.8 nm). Five concentrations of protein were subjected to SAXS as static samples (96-well plate) at the Australian Synchrotron. Subtle concentration dependent effects were noted. All data and additional information relating to the concentration series is included in the full-entry zip archive. The protein was subjected to SEC (off line) as the last purification step just prior to data collection. Also refer to the related SASBDB entry SASDDQ4.

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · LIM/homeobox protein Lhx4 LIM domains fused to the LIM interaction domain (LID) R282G mutant of Insulin gene enhancer protein ISL-2

浓度0.2 – 1.9 缓冲液 / pH20 mM Tris, 150 mM NaCl, 1 mM TCEP / 8.0
实验温度13.5 设备 / 束线Australian Synchrotron / SAXS/WAXS
波长0.10332 nm曝光1.0 s × 24

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
LIM/homeobox protein Lhx4
查看序列
GSMQQIPQCAGCNQHILDKFILKVLDRHWHSSCLKCADCQMQLADRCFSRAGSVYCKEDFFKRFGTKCTACQQGIPPTQVVRKAQDFVYHLHCFACIICNRQLATGDEFYLMEDGRLVCKEDYETAKQ
proteinMus musculusP5377624–149monomer分子数 114.712 kDa
Insulin gene enhancer protein ISL-2 (R282G)
查看序列
GGSGGHMGSGGGTPLVAGSPIGHENAVQGSAVEVQTYQPPW
proteinMus musculusQ9CXV0273–301monomer分子数 13.932 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
1825[3]0.006439803–0.3276825 1/A含误差列缺失 01sasbdb/entries/r4/sasddr4/source/SASDDR4.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)8.47—Å
i0Guinier0.033944e-05arbitrary
i0P(r)0.034095e-05arbitrary
mwExperimental15.0—kDa
mwGuinier I(0)17.0—kDa
porod_volumePorod20.7—ų
rgGuinier2.270.01Å
rgP(r)2.360.005Å

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20 mM Tris, 150 mM NaCl, 1 mM TCEP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2015-11-19储存 / 测量温度— / 13.5
曝光时间1.0帧数24
波长0.10332样品-探测器距离—
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线Australian Synchrotron / SAXS/WAXS · Melbourne, Australia
q 范围0.064 – 3.277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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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:186 个字段值
字段路径原始值
codeSASDDR4
statusPublished
type_of_curveExtrapolated to infinite dilution
angular_unit1/A
project.titleMutation in a flexible linker modulates binding affinity for modular complexes.
project.publication.titleMutation in a flexible linker modulates binding affinity for modular complexes.
project.publication.author_listStokes PH, Robertson NO, Silva AP, Estephan T, Trewhella J, Guss JM, Matthews JM
project.publication.journalProteins
project.publication.doi10.1002/prot.25675
project.publication.pmid30788856
project.publication.published_date2019 Feb 20
project.statusreleased
project.submitted_date2017-09-27
project.released_date2019-03-01
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experiment.instrument.detector.typeDectris
experiment.instrument.detector.namePilatus 1M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameAustralian Synchrotron
experiment.instrument.cityMelbourne
experiment.instrument.countryAustralia
experiment.instrument.beamline_nameSAXS/WAXS
experiment.instrument.beam_geometryPoint
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourceTrue
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_nameLIM/homeobox protein Lhx4
experiment.sample.molecule[0].short_nameLhx4-LIM domains
experiment.sample.molecule[0].sequenceGSMQQIPQCAGCNQHILDKFILKVLDRHWHSSCLKCADCQMQLADRCFSRAGSVYCKEDFFKRFGTKCTACQQGIPPTQVVRKAQDFVYHLHCFACIICNRQLATGDEFYLMEDGRLVCKEDYETAKQ
experiment.sample.molecule[0].organismMus musculus
experiment.sample.molecule[0].uniprot_codeP53776
experiment.sample.molecule[0].uniprot_range_first24
experiment.sample.molecule[0].uniprot_range_last149
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMMQSAAVPAEGAVKGLPEMLGVPMQQIPQCAGCNQHILDKFILKVLDRHWHSSCLKCADC QMQLADRCFSRAGSVYCKEDFFKRFGTKCTACQQGIPPTQVVRKAQDFVYHLHCFACIIC NRQLATGDEFYLMEDGRLVCKEDYETAKQNDDSEAGAKRPRTTITAKQLETLKNAYKNSP KPARHVREQLSSETGLDMRVVQVWFQNRRAKEKRLKKDAGRHRWGQFYKSVKRSRGGSKQ EKESSAEDCGVSDSELSFREDQILSELGHTNRIYGNVGDVTGGQLMNGSFSMDGTGQSYQ DLRDGSPYGIPQSPSSISSLPSHAPLLNGLDYTVDSNLGIIAHAGQGVSQTLRAMAGGPT SDLSTGSSVGYPDFPTSPASWLDEMDHPPF
experiment.sample.molecule[0].mw14.712
experiment.sample.molecule[0].total_mw14.712
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_nameInsulin gene enhancer protein ISL-2 (R282G)
experiment.sample.molecule[1].short_nameISL-2 (R282G)
experiment.sample.molecule[1].sequenceGGSGGHMGSGGGTPLVAGSPIGHENAVQGSAVEVQTYQPPW
experiment.sample.molecule[1].organismMus musculus
experiment.sample.molecule[1].uniprot_codeQ9CXV0
experiment.sample.molecule[1].uniprot_range_first273
experiment.sample.molecule[1].uniprot_range_last301
experiment.sample.molecule[1].oligomerizationmonomer
experiment.sample.molecule[1].molecular_typeprotein
experiment.sample.molecule[1].uniprot_sequenceMVDIIFHYPFLGAMGDHSKKKPGTAMCVGCGSQIHDQFILRVSPDLEWHAACLKCAECSQ YLDETCTCFVRDGKTYCKRDYVRLFGIKCAQCQVGFSSSDLVMRARDSVYHIECFRCSVC SRQLLPGDEFSLREHELLCRADHGLLLERAAAGSPRSPGPLPGARGLHLPDAGSGRQPSL RTHVHKQAEKTTRVRTVLNEKQLHTLRTCYAANPRPDALMKEQLVEMTGLSPRVIRVWFQ NKRCKDKKKSILMKQLQQQQHSDKASLQGLTGTPLVAGSPIRHENAVQGSAVEVQTYQPP WKALSEFALQSDLDQPAFQQLVSFSESGSLGNSSGSDVTSLSSQLPDTPNSMVPSPVET
experiment.sample.molecule[1].mw3.932
experiment.sample.molecule[1].total_mw3.932
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.buffer.name20 mM Tris, 150 mM NaCl, 1 mM TCEP
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.nameLIM/homeobox protein Lhx4 LIM domains fused to the LIM interaction domain (LID) R282G mutant of Insulin gene enhancer protein ISL-2
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].addressSydney, Australia
experiment.contributor[0].affiliation[0].full_nameSchool of Life and Environmental Science, University of Sydney
experiment.contributor[0].affiliation[0].webpagehttp://sydney.edu.au/science/life-environment/
experiment.contributor[0].contributor_namePhilippa
experiment.contributor[0].contributor_surnameStokes
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2015-11-19
experiment.storage_temperaturenull
experiment.cell_temperature13.5
experiment.exposure_time1.0
experiment.number_of_frames24
experiment.wavelength0.10332
experiment.sample_detector_distancenull
experiment.concentration_min0.2
experiment.concentration_max1.9
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.064
experiment.s_max3.277
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].p_value0.549514
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fits[0].software_versionnull
fits[0].descriptionnull
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionThe protein anaysed is a fusion of two interacting partners: the LIM domains of Lhx4 and the LID of Isl2, with a point mutation within the Isl2-LID (R282G). The ab initio bead models presented in this entry include: 1) The best-fit individual reconstruction (top) and; 2) The spatially aligned and volume/bead occupancy-corrected averaged representation of the protein in solution (bottom) calculated from twenty individual reconstructions (NSD = 0.67; resolution estimate = 2.8 nm). Five concentrations of protein were subjected to SAXS as static samples (96-well plate) at the Australian Synchrotron. Subtle concentration dependent effects were noted. All data and additional information relating to the concentration series is included in the full-entry zip archive. The protein was subjected to SEC (off line) as the last purification step just prior to data collection. Also refer to the related SASBDB entry SASDDQ4.
experiment_descriptionSynchrotron SAXS data from solutions of the LIM domains of LIM/homeobox protein Lhx4 fused to the LIM interaction domain (LID; R282G mutant) of the insulin gene enhancer protein ISL-2 in 20 mM Tris, 150 mM NaCl, 1 mM TCEP, pH 8 were collected on the SAXS/WAXS beam line at the Australian Synchrotron (Melbourne, Australia) using a Pilatus 1M detector at a wavelength of λ = 0.10332 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Solute concentrations ranging between 0.2 and 1.9 mg/ml were measured at 13.5°C. 24 successive 1 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. The low angle data collected at lower concentrations were extrapolated to infinite dilution and merged with the higher concentration data to yield the final composite scattering curve.
tags[]
intensity_unitarbitrary
experimental_mw15.0
experimental_mw_errornull
guinier_i0_mw17.0
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
pddf_i00.03409
pddf_i0_error5e-05
guinier_i00.03394
guinier_i0_error4e-05
pddf_rg2.36
pddf_rg_error0.005
guinier_rg2.27
guinier_rg_error0.01
pddf_dmax8.47
pddf_dmax_errornull
porod_volume20.7
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first10
guinier_point_last131
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDDR4_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 个字段值
字段路径原始值
codeSASDDR4
statussuccess
started_at2026-08-11T14:29:19.677540+00:00
finished_at2026-08-11T14:29:29.682470+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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查看完整 summary.json 原文
{
  "code": "SASDDR4",
  "status": "Published",
  "type_of_curve": "Extrapolated to infinite dilution",
  "angular_unit": "1/A",
  "project": {
    "title": "Mutation in a flexible linker modulates binding affinity for modular complexes.",
    "publication": {
      "title": "Mutation in a flexible linker modulates binding affinity for modular complexes.",
      "author_list": "Stokes PH, Robertson NO, Silva AP, Estephan T, Trewhella J, Guss JM, Matthews JM",
      "journal": "Proteins",
      "doi": "10.1002/prot.25675",
      "pmid": "30788856",
      "published_date": "2019 Feb 20"
    },
    "status": "released",
    "submitted_date": "2017-09-27",
    "released_date": "2019-03-01"
  },
  "pddf_data": "https://www.sasbdb.org/media/p_of_R_files/SASDDR4.out",
  "intensities_data": "https://www.sasbdb.org/media/intensities_files/SASDDR4.dat",
  "intensities_log_plot": "https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDDR4_dat_img.png",
  "intensities_kratky_plot": "https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDDR4_kratky_img.png",
  "pddf_plot": "https://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDDR4_pofr_img.png",
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  "experiment": {
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      "detector": {
        "type": "Dectris",
        "name": "Pilatus 1M",
        "resolution": 172.0
      },
      "name": "Australian  Synchrotron",
      "city": "Melbourne",
      "country": "Australia",
      "beamline_name": "SAXS/WAXS",
      "beam_geometry": "Point",
      "type_of_source": "X-ray synchrotron",
      "point_source": true,
      "line_collimation": null,
      "sample_path_length": null,
      "line_collimation_slitlength": null,
      "line_collimation_integrationwidth": null,
      "xray_energy": null,
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      "beam_profile_al": null
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      "molecule": [
        {
          "long_name": "LIM/homeobox protein Lhx4",
          "short_name": "Lhx4-LIM domains",
          "sequence": "GSMQQIPQCAGCNQHILDKFILKVLDRHWHSSCLKCADCQMQLADRCFSRAGSVYCKEDFFKRFGTKCTACQQGIPPTQVVRKAQDFVYHLHCFACIICNRQLATGDEFYLMEDGRLVCKEDYETAKQ",
          "organism": "Mus musculus",
          "uniprot_code": "P53776",
          "uniprot_range_first": 24,
          "uniprot_range_last": 149,
          "oligomerization": "monomer",
          "molecular_type": "protein",
          "uniprot_sequence": "MMQSAAVPAEGAVKGLPEMLGVPMQQIPQCAGCNQHILDKFILKVLDRHWHSSCLKCADC\nQMQLADRCFSRAGSVYCKEDFFKRFGTKCTACQQGIPPTQVVRKAQDFVYHLHCFACIIC\nNRQLATGDEFYLMEDGRLVCKEDYETAKQNDDSEAGAKRPRTTITAKQLETLKNAYKNSP\nKPARHVREQLSSETGLDMRVVQVWFQNRRAKEKRLKKDAGRHRWGQFYKSVKRSRGGSKQ\nEKESSAEDCGVSDSELSFREDQILSELGHTNRIYGNVGDVTGGQLMNGSFSMDGTGQSYQ\nDLRDGSPYGIPQSPSSISSLPSHAPLLNGLDYTVDSNLGIIAHAGQGVSQTLRAMAGGPT\nSDLSTGSSVGYPDFPTSPASWLDEMDHPPF",
          "mw": 14.712,
          "total_mw": 14.712,
          "number_molecules": 1,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        },
        {
          "long_name": "Insulin gene enhancer protein ISL-2 (R282G)",
          "short_name": "ISL-2 (R282G)",
          "sequence": "GGSGGHMGSGGGTPLVAGSPIGHENAVQGSAVEVQTYQPPW",
          "organism": "Mus musculus",
          "uniprot_code": "Q9CXV0",
          "uniprot_range_first": 273,
          "uniprot_range_last": 301,
          "oligomerization": "monomer",
          "molecular_type": "protein",
          "uniprot_sequence": "MVDIIFHYPFLGAMGDHSKKKPGTAMCVGCGSQIHDQFILRVSPDLEWHAACLKCAECSQ\nYLDETCTCFVRDGKTYCKRDYVRLFGIKCAQCQVGFSSSDLVMRARDSVYHIECFRCSVC\nSRQLLPGDEFSLREHELLCRADHGLLLERAAAGSPRSPGPLPGARGLHLPDAGSGRQPSL\nRTHVHKQAEKTTRVRTVLNEKQLHTLRTCYAANPRPDALMKEQLVEMTGLSPRVIRVWFQ\nNKRCKDKKKSILMKQLQQQQHSDKASLQGLTGTPLVAGSPIRHENAVQGSAVEVQTYQPP\nWKALSEFALQSDLDQPAFQQLVSFSESGSLGNSSGSDVTSLSSQLPDTPNSMVPSPVET",
          "mw": 3.932,
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          "number_molecules": 1,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": null
        }
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      "buffer": {
        "name": "20 mM Tris, 150 mM NaCl, 1 mM TCEP",
        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 8.0,
        "deuteration": null
      },
      "purity_method": null,
      "name": "LIM/homeobox protein Lhx4 LIM domains fused to the LIM interaction domain (LID) R282G mutant of Insulin gene enhancer protein ISL-2",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": null,
            "address": "Sydney, Australia",
            "full_name": "School of Life and Environmental Science, University of Sydney",
            "webpage": "http://sydney.edu.au/science/life-environment/"
          }
        ],
        "contributor_name": "Philippa",
        "contributor_surname": "Stokes",
        "orcid": null
      }
    ],
    "concentration_method": null,
    "concentration_unit": null,
    "date": "2015-11-19",
    "storage_temperature": null,
    "cell_temperature": 13.5,
    "exposure_time": 1.0,
    "number_of_frames": 24,
    "wavelength": 0.10332,
    "sample_detector_distance": null,
    "concentration_min": 0.2,
    "concentration_max": 1.9,
    "sample_volume": null,
    "flow_rate": null,
    "s_min": 0.064,
    "s_max": 3.277,
    "total_exposure_time": null,
    "seccolumn": null
  },
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          "software": "DAMMIN",
          "pdb_link": [],
          "model_title": null,
          "type_of_model": "dummy",
          "software_version": null,
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDDR4_fit1_model1.pdb",
          "model_mw": 13.802,
          "bead_radius": 2.2,
          "log": null,
          "symmetry": null,
          "comment": "One of 20 models generated using DAMMIN that went into creating the Damfilt model.",
          "user": 205
        },
        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDDR4_fit1_model2_img.png",
          "software": "DAMFILT",
          "pdb_link": [],
          "model_title": null,
          "type_of_model": "dummy",
          "software_version": null,
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDDR4_fit1_model2.pdb",
          "model_mw": 13.721,
          "bead_radius": 2.0,
          "log": "https://www.sasbdb.org/media/log_files/damsup_Dn1jpbJ.log",
          "symmetry": null,
          "comment": "Damfilt model derived from multiple DAMMIN runs where 20 models were generated, spatially aligned.",
          "user": 205
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      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/DM7GExtr_fit_img.png",
      "software": "DAMMIN",
      "chi_square_value": 4.442,
      "p_value": 0.549514,
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      "software_version": null,
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  "estimated_volume_method": null,
  "pddf_software": "ATSAS GNOM",
  "pddf_software_version": "5.0",
  "i0_calibration_standard": null,
  "description": "The protein anaysed is a fusion of two interacting partners: the LIM domains of Lhx4 and the LID of Isl2, with a point mutation within the Isl2-LID (R282G). The ab initio bead models presented in this entry include: 1) The best-fit individual reconstruction (top) and; 2) The spatially aligned and volume/bead occupancy-corrected averaged representation of the protein in solution (bottom) calculated from twenty individual reconstructions (NSD = 0.67; resolution estimate = 2.8 nm). Five concentrations of protein were subjected to SAXS as static samples (96-well plate) at the Australian Synchrotron. Subtle concentration dependent effects were noted. All data and additional information relating to the concentration series is included in the full-entry zip archive. The protein was subjected to SEC (off line) as the last purification step just prior to data collection. Also refer to the related SASBDB entry SASDDQ4.",
  "experiment_description": "Synchrotron SAXS data from solutions of the LIM domains of LIM/homeobox protein Lhx4 fused to the LIM interaction domain (LID; R282G mutant) of the insulin gene enhancer protein ISL-2 in 20 mM Tris, 150 mM NaCl, 1 mM TCEP, pH 8 were collected on the SAXS/WAXS beam line at the Australian Synchrotron (Melbourne, Australia) using a Pilatus 1M detector at a wavelength of λ = 0.10332 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Solute concentrations ranging between 0.2 and 1.9 mg/ml were measured at 13.5°C. 24 successive 1 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. The low angle data collected at lower concentrations were extrapolated to infinite dilution and merged with the higher concentration data to yield the final composite scattering curve.",
  "tags": [],
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  "experimental_mw_error": null,
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  "pddf_i0_error": 5e-05,
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  "guinier_i0_error": 4e-05,
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  "guinier_rg_error": 0.01,
  "pddf_dmax": 8.47,
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  "porod_volume": 20.7,
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  "estimated_volume": null,
  "estimated_volume_error": null,
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  "intensities_log_log_plot": "SASDDR4_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2019-12-06T13:07:15.624532+01:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
{
  "code": "SASDDR4",
  "status": "success",
  "started_at": "2026-08-11T14:29:19.677540+00:00",
  "finished_at": "2026-08-11T14:29:29.682470+00:00",
  "source_last_modified": "2019-12-06T13:07:15.624532+01:00",
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