SASDFP8

Carbonic anhydrase 2 from bovine erythrocytes - SEC-SAXS coupled to multiangle laser and quasi-elastic light scattering (MALLS and QELS)

数据类型:SASBDB 实验数据 状态:Published 曲线类型:SEC-SAS 最后更新:2023-06-21T07:55:24.740692+02:00

Carbonic anhydrase underwent pre-purification prior to SEC-SAXS using the following method. All procedures were performed at 4 oC. The protein (from Sigma; Gel Filtration Markers Kit MWGF1000) was made to approximately 25 mg/ml in 25 mM HEPES, 50 mM NaCl, 5 mM urea, 1% v/v glycerol, pH 7. Approximately 200 μl of sample were loaded onto a Superdex 75 Increase 10/300 column (GE Healthcare) equilibrated in the same buffer (flow rate = 0.4 ml/min). Fractionated aliquots corresponding to the highest absorbing peak (estimated using UV A280 and UV A245 nm) were pooled and concentrated (3 kDa centrifuge spin filter) to a final concentration of 11.9 mg/ml (the concentration was determined from triplicate UV A280 measurements using an E0.1% of 1.732 (= 1 g/l) calculated from the amino acid sequence (ProtParam)). Approximately 50 μl aliquots were snap-frozen in liquid nitrogen then stored at -80oC prior to the SEC-SAXS analysis that was performed at room temperature in 50 mM HEPES, 150 mM NaCl, 2% v/v glycerol, pH 7. The Rg-correlation through the SEC-SAXS peak, the individual unsubtracted SEC-SAXS frames as well as the results from coupled MALLS and QELS analysis are included in the full entry zip archive. The quoted experimental molecular weight was determined using MALLS in combination with refractive-index (RI) measurements that were recorded from the same sample eluting from the column using a split-flow SEC-SAXS-light scattering configuration (Graewert et al., (2015) Sci. Reports. 5, 10734: doi: 10.1038/srep10734). The average hydrodynamic radius of the protein is 2.4 nm.

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Carbonic anhydrase 2 from bovine erythrocytes - SEC-SAXS coupled to multiangle laser and quasi-elastic light scattering (MALLS and QELS)

浓度— – 11.9 缓冲液 / pH50 mM HEPES, 150 mM NaCl, 2% v/v glycerol / 7.0
实验温度20.0 设备 / 束线PETRA III / EMBL P12
波长0.123982 nm曝光1.0 s × 41

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Carbonic anhydrase 2
查看序列
MSHHWGYGKHNGPEHWHKDFPIANGERQSPVDIDTKAVVQDPALKPLALVYGEATSRRMVNNGHSFNVEYDDSQDKAVLKDGPLTGTYRLVQFHFHWGSSDDQGSEHTVDRKKYAAELHLVHWNTKYGDFGTAAQQPDGLAVVGVFLKVGDANPALQKVLDALDSIKTKGKSTDFPNFDPGSLLPNVLDYWTYPGSLTTPPLLESVTWIVLKEPISVSSQQMLKFRTLNFNAEGEPELLMLANWRPAQPLKNRQVRGFPK
proteinBos taurusP009211–260monomer分子数 129.113 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
12584[3]0.072981–7.21299 1/nm含误差列缺失 016sasbdb/entries/p8/sasdfp8/source/SASDFP8.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)5.05—nm
i0Guinier7753.83.15arbitrary
i0P(r)7744.02.5arbitrary
mwExperimental28.3—kDa
mwPorod23.0—kDa
porod_volumePorod36.7—nm³
rgGuinier1.82—nm
rgP(r)1.7920.001nm

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 · DAMMIN

χ²:1.02CorMap p:0.448891单位:1/A

Fit of refined DAMMIN model obtained from the spatial alignment of 10 individual models that fit the SAXS data.

模型名称 / 类型软件对称性模型 MWPDB 声明来源文件
1—dummyDAMMIN SUPCOMB 23 (r9988)P122.648—模型 图片
2—dummyDAMFILT DAMFILT 5.0 (r10552)P122.209—模型 图片

拟合 2 · CRYSOL CRYSOL_30

χ²:1.095CorMap p:0.269894单位:1/A

CRYSOL_30 fit calculated with 30 harmonics and 300 points

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) P128.965A25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 HEPES, 150 mM NaCl, 2% v/v glycerol缓冲液浓度—
pH7.0添加剂—
缓冲液说明Running buffer for SEC-SAXS
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2019-04-05储存 / 测量温度20.0 / 20.0
曝光时间1.0帧数41
波长0.123982样品-探测器距离3.0
光源X-ray synchrotron探测器Pilatus 6M
机构 / 束线PETRA III / EMBL P12 · DESY; Hamburg, Germany
q 范围0.073 – 7.213样品体积 / 流速100.0 / 0.5

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/p8/sasdfp8/source/SASDFP8.outdownloaded15164636cc826fca009f8034c4d701a1a6f95a696559c3c04df4cabe9f0d78dbbbdb6e下载查看原文件源站
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summarysasbdb/entries/p8/sasdfp8/source/summary.jsondownloaded12299c3ebedef925cdd86a8e930635aed1759737716734b215471af2eaceb1e316663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(10 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:202 个字段值
字段路径原始值
codeSASDFP8
statusPublished
type_of_curveSEC-SAS
angular_unit1/nm
project.titleAdding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data
project.publication.titleAdding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data
project.publication.author_listGraewert M, Da Vela S, Gräwert T, Molodenskiy D, Blanchet C, Svergun D, Jeffries C
project.publication.journalCrystals
project.publication.doi10.3390/cryst10110975
project.publication.pmidnull
project.publication.published_date2020 Oct 27
project.statusreleased
project.submitted_date2019-07-10
project.released_date2019-07-10
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDFP8.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDFP8.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFP8_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFP8_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDFP8_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFP8_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDFP8.sascif
experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus 6M
experiment.instrument.detector.resolutionnull
experiment.instrument.namePETRA III
experiment.instrument.cityDESY; Hamburg
experiment.instrument.countryGermany
experiment.instrument.beamline_nameEMBL P12
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_nameCarbonic anhydrase 2
experiment.sample.molecule[0].short_nameCA2
experiment.sample.molecule[0].sequenceMSHHWGYGKHNGPEHWHKDFPIANGERQSPVDIDTKAVVQDPALKPLALVYGEATSRRMV NNGHSFNVEYDDSQDKAVLKDGPLTGTYRLVQFHFHWGSSDDQGSEHTVDRKKYAAELHL VHWNTKYGDFGTAAQQPDGLAVVGVFLKVGDANPALQKVLDALDSIKTKGKSTDFPNFDP GSLLPNVLDYWTYPGSLTTPPLLESVTWIVLKEPISVSSQQMLKFRTLNFNAEGEPELLM LANWRPAQPLKNRQVRGFPK
experiment.sample.molecule[0].organismBos taurus
experiment.sample.molecule[0].uniprot_codeP00921
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last260
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMSHHWGYGKHNGPEHWHKDFPIANGERQSPVDIDTKAVVQDPALKPLALVYGEATSRRMV NNGHSFNVEYDDSQDKAVLKDGPLTGTYRLVQFHFHWGSSDDQGSEHTVDRKKYAAELHL VHWNTKYGDFGTAAQQPDGLAVVGVFLKVGDANPALQKVLDALDSIKTKGKSTDFPNFDP GSLLPNVLDYWTYPGSLTTPPLLESVTWIVLKEPISVSSQQMLKFRTLNFNAEGEPELLM LANWRPAQPLKNRQVRGFPK
experiment.sample.molecule[0].mw29.113
experiment.sample.molecule[0].total_mw29.113
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.name50 mM HEPES, 150 mM NaCl, 2% v/v glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentRunning buffer for SEC-SAXS
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameCarbonic anhydrase 2 from bovine erythrocytes - SEC-SAXS coupled to multiangle laser and quasi-elastic light scattering (MALLS and QELS)
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_nameEMBL-Hamburg
experiment.contributor[0].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[0].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[0].contributor_nameMelissa
experiment.contributor[0].contributor_surnameGraewert
experiment.contributor[0].orcidnull
experiment.contributor[1].affiliation[0].short_nameEMBL-Hamburg
experiment.contributor[1].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[1].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[1].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[1].contributor_nameCy M
experiment.contributor[1].contributor_surnameJeffries
experiment.contributor[1].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2019-04-05
experiment.storage_temperature20.0
experiment.cell_temperature20.0
experiment.exposure_time1.0
experiment.number_of_frames41
experiment.wavelength0.123982
experiment.sample_detector_distance3.0
experiment.concentration_minnull
experiment.concentration_max11.9
experiment.sample_volume100.0
experiment.flow_rate0.5
experiment.s_min0.073
experiment.s_max7.213
experiment.total_exposure_timenull
experiment.seccolumn3
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDFP8_fit1_model1_img.png
fits[0].models[0].softwareDAMMIN
fits[0].models[0].pdb_link[]
fits[0].models[0].model_titlenull
fits[0].models[0].type_of_modeldummy
fits[0].models[0].software_versionSUPCOMB 23 (r9988)
fits[0].models[0].model_datahttps://www.sasbdb.org/media/pdb_file/SASDFP8_fit1_model1.pdb
fits[0].models[0].model_mw22.648
fits[0].models[0].bead_radius1.5
fits[0].models[0].lognull
fits[0].models[0].symmetryP1
fits[0].models[0].commentRefined DAMMIN model obtained from the spatial alignment of 10 individual models (DAMSTART)
fits[0].models[0].user9
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fits[0].models[1].softwareDAMFILT
fits[0].models[1].pdb_link[]
fits[0].models[1].model_titlenull
fits[0].models[1].type_of_modeldummy
fits[0].models[1].software_versionDAMFILT 5.0 (r10552)
fits[0].models[1].model_datahttps://www.sasbdb.org/media/pdb_file/SASDFP8_fit1_model2.pdb
fits[0].models[1].model_mw22.209
fits[0].models[1].bead_radius1.5
fits[0].models[1].lognull
fits[0].models[1].symmetryP1
fits[0].models[1].commentDAMFILT spatially aligned and volume occupancy corrected (averaged) model from 10 individual models
fits[0].models[1].user9
fits[0].fit_unit1/A
fits[0].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/SASDFP8_fit1_fixed_fit_img.png
fits[0].softwareDAMMIN
fits[0].chi_square_value1.02
fits[0].p_value0.448891
fits[0].fit_residual_plotSASDFP8_fit1_fitresiduals_img.png
fits[0].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDFP8_fit1.fir
fits[0].fit_loghttps://www.sasbdb.org/media/fitting_files/log_files/refine_0U0OuhM.log
fits[0].software_versionnull
fits[0].descriptionFit of refined DAMMIN model obtained from the spatial alignment of 10 individual models that fit the SAXS data.
fits[1].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDFP8_fit2_model1_img.png
fits[1].models[0].softwarePDB (Protein Data Bank)
fits[1].models[0].pdb_link[0].pdb_code5a25
fits[1].models[0].pdb_link[0].ext_code5A25
fits[1].models[0].pdb_link[0].ext_typepdb
fits[1].models[0].pdb_link[0].difference_with_modelderived
fits[1].models[0].model_titlenull
fits[1].models[0].type_of_modelatomic
fits[1].models[0].software_versionnull
fits[1].models[0].model_datahttps://www.sasbdb.org/media/pdb_file/SASDFP8_fit2_model1.pdb
fits[1].models[0].model_mw28.96
fits[1].models[0].bead_radiusnull
fits[1].models[0].lognull
fits[1].models[0].symmetryP1
fits[1].models[0].commentModel-fit calculated using 30 harmonics and 300 points
fits[1].models[0].user9
fits[1].fit_unit1/A
fits[1].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/SASDFP8_fit2_fixed_fit_img.png
fits[1].softwareCRYSOL
fits[1].chi_square_value1.095
fits[1].p_value0.269894
fits[1].fit_residual_plotSASDFP8_fit2_fitresiduals_img.png
fits[1].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDFP8_fit2.fit
fits[1].fit_loghttps://www.sasbdb.org/media/fitting_files/log_files/5a25_monomerr00.log
fits[1].software_versionCRYSOL_30
fits[1].descriptionCRYSOL_30 fit calculated with 30 harmonics and 300 points
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionCarbonic anhydrase underwent pre-purification prior to SEC-SAXS using the following method. All procedures were performed at 4 oC. The protein (from Sigma; Gel Filtration Markers Kit MWGF1000) was made to approximately 25 mg/ml in 25 mM HEPES, 50 mM NaCl, 5 mM urea, 1% v/v glycerol, pH 7. Approximately 200 μl of sample were loaded onto a Superdex 75 Increase 10/300 column (GE Healthcare) equilibrated in the same buffer (flow rate = 0.4 ml/min). Fractionated aliquots corresponding to the highest absorbing peak (estimated using UV A280 and UV A245 nm) were pooled and concentrated (3 kDa centrifuge spin filter) to a final concentration of 11.9 mg/ml (the concentration was determined from triplicate UV A280 measurements using an E0.1% of 1.732 (= 1 g/l) calculated from the amino acid sequence (ProtParam)). Approximately 50 μl aliquots were snap-frozen in liquid nitrogen then stored at -80oC prior to the SEC-SAXS analysis that was performed at room temperature in 50 mM HEPES, 150 mM NaCl, 2% v/v glycerol, pH 7. The Rg-correlation through the SEC-SAXS peak, the individual unsubtracted SEC-SAXS frames as well as the results from coupled MALLS and QELS analysis are included in the full entry zip archive. The quoted experimental molecular weight was determined using MALLS in combination with refractive-index (RI) measurements that were recorded from the same sample eluting from the column using a split-flow SEC-SAXS-light scattering configuration (Graewert et al., (2015) Sci. Reports. 5, 10734: doi: 10.1038/srep10734). The average hydrodynamic radius of the protein is 2.4 nm.
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last_modified2023-06-21T07:55:24.740692+02:00
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查看完整 summary.json 原文
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  "status": "Published",
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  "angular_unit": "1/nm",
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    "title": "Adding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data",
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      "title": "Adding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data",
      "author_list": "Graewert M, Da Vela S, Gräwert T, Molodenskiy D, Blanchet C, Svergun D, Jeffries C",
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      "doi": "10.3390/cryst10110975",
      "pmid": null,
      "published_date": "2020 Oct 27"
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查看完整 manifest.json 原文
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