SASDWU6

Human anterior gradient protein 2 (AGR2)

数据类型:SASBDB 实验数据 状态:Published 曲线类型:SEC-SAS 最后更新:2025-10-27T12:08:22.283589+01:00
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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Human anterior gradient protein 2 (AGR2)

浓度— – 46.0 缓冲液 / pH20 mM Tris pH7.4, 150 mM NaCl, 1% glycerol, 0.2 mM TCEP / 7.4
实验温度15.0 设备 / 束线Diamond Light Source / B21
波长0.09464 nm曝光1.0 s × 30

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Anterior gradient protein 2 homolog
查看序列
PQTLSRGWGDQLIWTQTYEEALYKSKTSNKPLMIIHHLDECPHSQALKKVFAENKEIQKLAEQFVLLNLVYETTDKHLSPDGQYVPRIMFVDPSLTVRADITGRYSNRLYAYEPADTALLLDNMKKALKLL
proteinHomo sapiensO9599441–171dimer分子数 215.122 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
12568[3]0.0045–0.34 1/A含误差列缺失 00sasbdb/entries/u6/sasdwu6/source/SASDWU6.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)6.27—Å
i0Guinier0.177626—1/cm
i0P(r)0.1785—1/cm
mwExperimental24.4—kDa
mwPorod18.7—kDa
porod_volumePorod29.9—ų
rgGuinier1.9550.011Å
rgP(r)1.980.018Å

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 pH7.4, 150 mM NaCl, 1% glycerol, 0.2 mM TCEP缓冲液浓度—
pH7.4添加剂—
缓冲液说明The buffer for SEC runs was the same as the sample buffer.
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2024-05-05储存 / 测量温度15.0 / 15.0
曝光时间1.0帧数30
波长0.09464样品-探测器距离3.6929
光源X-ray synchrotron探测器Eiger 4M
机构 / 束线Diamond Light Source / B21 · Didcot, UK
q 范围0.045 – 3.4样品体积 / 流速35.0 / 0.06

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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full_entry_zipsasbdb/entries/u6/sasdwu6/source/SASDWU6.zipdownloaded197004b05165e0df4d395ac4c4b8196df5b74943b704ec8ecf8597d9c03f089edb05a8下载查看原文件源站
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sascifsasbdb/entries/u6/sasdwu6/source/SASDWU6.sascifnot_available——下载查看原文件源站
summarysasbdb/entries/u6/sasdwu6/source/summary.jsondownloaded8099b1187791e303edd4a1b8c80dde76ae783e28a6f82ee179b47fab969786ef0e70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:169 个字段值
字段路径原始值
codeSASDWU6
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleA structural basis for chaperone repression of stress signaling from the endoplasmic reticulum.
project.publication.titleA structural basis for chaperone repression of stress signaling from the endoplasmic reticulum.
project.publication.author_listNeidhardt L, Tung J, Kuchersky M, Milczarek J, Kargas V, Stott K, Rosenzweig R, Ron D, Yan Y
project.publication.journalMol Cell
project.publication.doi10.1016/j.molcel.2025.09.032
project.publication.pmid41135511
project.publication.published_date2025 Oct 23
project.statusreleased
project.submitted_date2025-01-24
project.released_date2025-10-23
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experiment.instrument.detector.typenull
experiment.instrument.detector.nameEiger 4M
experiment.instrument.detector.resolution75.0
experiment.instrument.nameDiamond Light Source
experiment.instrument.cityDidcot
experiment.instrument.countryUK
experiment.instrument.beamline_nameB21
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_nameAnterior gradient protein 2 homolog
experiment.sample.molecule[0].short_nameAGR2
experiment.sample.molecule[0].sequencePQTLSRGWGDQLIWTQTYEEALYKSKTSNKPLMIIHHLDECPHSQALKKVFAENKEIQKLAEQFVLLNLVYETTDKHLSPDGQYVPRIMFVDPSLTVRADITGRYSNRLYAYEPADTALLLDNMKKALKLL
experiment.sample.molecule[0].organismHomo sapiens
experiment.sample.molecule[0].uniprot_codeO95994
experiment.sample.molecule[0].uniprot_range_first41
experiment.sample.molecule[0].uniprot_range_last171
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMEKIPVSAFLLLVALSYTLARDTTVKPGAKKDTKDSRPKLPQTLSRGWGDQLIWTQTYEE ALYKSKTSNKPLMIIHHLDECPHSQALKKVFAENKEIQKLAEQFVLLNLVYETTDKHLSP DGQYVPRIMFVDPSLTVRADITGRYSNRLYAYEPADTALLLDNMKKALKLLKTEL
experiment.sample.molecule[0].mw15.122
experiment.sample.molecule[0].total_mw30.244
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_descriptionRequired for MUC2 post-transcriptional synthesis and secretion.
experiment.sample.buffer.name20 mM Tris pH7.4, 150 mM NaCl, 1% glycerol, 0.2 mM TCEP
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentThe buffer for SEC runs was the same as the sample buffer.
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.4
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameHuman anterior gradient protein 2 (AGR2)
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].addressnull
experiment.contributor[0].affiliation[0].full_nameUniversity of Cambridge
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameYahui
experiment.contributor[0].contributor_surnameYan
experiment.contributor[0].orcidhttps://orcid.org/0000-0001-6934-9874
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2024-05-05
experiment.storage_temperature15.0
experiment.cell_temperature15.0
experiment.exposure_time1.0
experiment.number_of_frames30
experiment.wavelength0.09464
experiment.sample_detector_distance3.6929
experiment.concentration_minnull
experiment.concentration_max46.0
experiment.sample_volume35.0
experiment.flow_rate0.06
experiment.s_min0.045
experiment.s_max3.4
experiment.total_exposure_timenull
experiment.seccolumn13
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fits[0].models[0].software_versionnull
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fits[0].chi_square_value4.229369
fits[0].p_value0.0
fits[0].fit_residual_plotSASDWU6_fit1_fitfoxsresiduals_img.png
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fits[0].fit_lognull
fits[0].software_versionnull
fits[0].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of anterior gradient protein 2 (AGR2) in 20 mM Tris pH7.4, 150 mM NaCl, 1% glycerol, 0.2 mM TCEP, were collected on the B21 beam line at the Diamond Light Source (Didcot, UK) using a Eiger 4M detector at a sample-detector distance of 3.7 m and at a wavelength of λ = 0.09464 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 35.00 μl sample at 46 mg/ml was injected at a 0.06 ml/min flow rate onto a GE Superdex 75 Increase 3.2/300 column at 15°C. 30 successive 1 second frames were collected through the sample elution peak (from a total of 600 frames collected throughout the entire SEC run). The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[]
intensity_unit1/cm
experimental_mw24.4
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw18.7
porod_mw_errornull
pddf_i00.1785
pddf_i0_errornull
guinier_i00.177626
guinier_i0_errornull
pddf_rg1.98
pddf_rg_error0.018
guinier_rg1.955
guinier_rg_error0.011
pddf_dmax6.27
pddf_dmax_errornull
porod_volume29.9
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first224
guinier_point_last473
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDWU6_datloglog_img.png
symmetrynull
last_modified2025-10-27T12:08:22.283589+01:00
bragg_peak[]
manifest.json:34 个字段值
字段路径原始值
codeSASDWU6
statussuccess
started_at2026-08-11T15:16:17.764370+00:00
finished_at2026-08-11T15:16:28.651993+00:00
source_last_modified2025-10-27T12:08:22.283589+01:00
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查看完整 summary.json 原文
{
  "code": "SASDWU6",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "A structural basis for chaperone repression of stress signaling from the endoplasmic reticulum.",
    "publication": {
      "title": "A structural basis for chaperone repression of stress signaling from the endoplasmic reticulum.",
      "author_list": "Neidhardt L, Tung J, Kuchersky M, Milczarek J, Kargas V, Stott K, Rosenzweig R, Ron D, Yan Y",
      "journal": "Mol Cell",
      "doi": "10.1016/j.molcel.2025.09.032",
      "pmid": "41135511",
      "published_date": "2025 Oct 23"
    },
    "status": "released",
    "submitted_date": "2025-01-24",
    "released_date": "2025-10-23"
  },
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          "sequence": "PQTLSRGWGDQLIWTQTYEEALYKSKTSNKPLMIIHHLDECPHSQALKKVFAENKEIQKLAEQFVLLNLVYETTDKHLSPDGQYVPRIMFVDPSLTVRADITGRYSNRLYAYEPADTALLLDNMKKALKLL",
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          "molecule_source": "biological",
          "molecule_description": "Required for MUC2 post-transcriptional synthesis and secretion."
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        "concentration": null,
        "pka": null,
        "ph": 7.4,
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      },
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查看完整 manifest.json 原文
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