SASDXG2

Probable conserved Mce associated membrane protein (Mam1Adelta106) from M.tuberculosis (SANS)

数据类型:SASBDB 实验数据 状态:Published 曲线类型:Single concentration 最后更新:2026-05-05T11:41:40.417306+02:00

SANS data were collected on the Zoom time-of-flight SANS instrument (ISIS Neutron and Muon Source, Harwell, UK) using wavelength range 1.75-16.5Å. The source to sample and sample to detector distance was 4 m and the beam size was 12 mm. Mam1Adelta106 was solubilized with C12E9 in the lysis buffer where the deuteration of the C12E9 was 0.2 % v/v. Excess C12E9 was washed away throughout the purification, and replaced with D-C12E9 in the STFC SANS facilities using SEC Superdex200 column. From the highest point of the peak, 3 fractions were selected. Each of these fractions was loaded to Starna Scientific quartz round cuvette (match code 6,path length 1, type 32/Q/1), and SANS data were collected from each fraction with an exposure time of 1 h in 5 cycles (5 h total exposure time for each fraction). The neutron momentum transfer (q) standard deviation and truncated scattering data are provided as an additional file.

1. 样品、组分与实验条件 Sample & Experiment

样品 1 · Probable conserved Mce associated membrane protein (Mam1Adelta106) from M.tuberculosis (SANS)

浓度— – — 缓冲液 / pH50 mM Tris, 500 mM NaCl, D-C12E9 / 8.5
实验温度6.0 设备 / 束线ISIS Neutron and Muon Source / SANS2D
波长— nm曝光— s × —

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Probable conserved Mce associated membrane protein
查看序列
MKHHHHHHPMSDYDIPTTENLYFQGAMAPDAGAMSASMQKIIECGTGDFGAQASLYTSMLVEAYQAASVHVQVTDMRAAVERNNNDGSVDVLVALRVKVSNTDSDAHEVGYRLRVRMALDEGRYKIAKLDQVTK
proteinMycobacterium tuberculosis (strain ATCC 25618 / H37Rv)O07419107–213tetramer分子数 414.807 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
164[3]0.00624–0.78266 1/A含误差列缺失 05sasbdb/entries/g2/sasdxg2/source/SASDXG2.dat

2. SASBDB 报告的指标 Reported Results

指标方法数值误差单位
dmaxP(r)8.5Å
i0Guinier0.124085arbitrary
i0P(r)0.126arbitrary
mwExperimental33.1kDa
mwPorod20.0kDa
porod_volumePorod70.0ų
rgGuinier2.5530.683Å
rgP(r)2.58Å

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。

3. 来源拟合与模型 Source Fits & Models

4. 来源文件索引 Source Files

5. 实验说明与论文 Experiment & Publication

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 Tris, 500 mM NaCl, D-C12E9缓冲液浓度
pH8.5添加剂
缓冲液说明50mM Tris at pH8.5 with 500mM NaCl, supplemented with 0.003% Deuterated C12E9
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2024-04-25储存 / 测量温度4.0 / 6.0
曝光时间帧数
波长样品-探测器距离
光源neutron source探测器
机构 / 束线ISIS Neutron and Muon Source / SANS2D · Didcot, UK
q 范围0.062 – 7.827样品体积 / 流速35.0 / 0.07

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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sascifsasbdb/entries/g2/sasdxg2/source/SASDXG2.sascifnot_available下载查看原文件源站
summarysasbdb/entries/g2/sasdxg2/source/summary.jsondownloaded8395f72f3b03b2aa1bc3db54688448e8cab931e1c3efce5efff3b6f7e80670401dea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(8 项)
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pddf:来源记录
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sascif: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:161 个字段值
字段路径原始值
codeSASDXG2
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleInsight into the structure and interactions of the <i>M. tuberculosis</i> Mce-associated membrane proteins Mam1A-1D
project.publication.titleInsight into the structure and interactions of the <i>M. tuberculosis</i> Mce-associated membrane proteins Mam1A-1D
project.publication.author_listHynönen M, Perumal P, Hynönen N, Doutch J, Ma K, Venkatesan R
project.publication.journalnull
project.publication.doi10.1101/2025.03.26.645568
project.publication.pmidnull
project.publication.published_date2025 Mar 26
project.statusreleased
project.submitted_date2025-03-26
project.released_date2025-04-11
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intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDXG2.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDXG2_dat_img.png
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pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDXG2_pofr_img.png
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experiment.instrument.detectornull
experiment.instrument.nameISIS Neutron and Muon Source
experiment.instrument.cityDidcot
experiment.instrument.countryUK
experiment.instrument.beamline_nameSANS2D
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_nameProbable conserved Mce associated membrane protein
experiment.sample.molecule[0].short_nameMam1A delta 106
experiment.sample.molecule[0].sequenceMKHHHHHHPMSDYDIPTTENLYFQGAMAPDAGAMSASMQKIIECGTGDFGAQASLYTSMLVEAYQAASVHVQVTDMRAAVERNNNDGSVDVLVALRVKVSNTDSDAHEVGYRLRVRMALDEGRYKIAKLDQVTK
experiment.sample.molecule[0].organismMycobacterium tuberculosis (strain ATCC 25618 / H37Rv)
experiment.sample.molecule[0].uniprot_codeO07419
experiment.sample.molecule[0].uniprot_range_first107
experiment.sample.molecule[0].uniprot_range_last213
experiment.sample.molecule[0].oligomerizationtetramer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMKAADSAESDAGADQTGPQVKAADSAESDAGELGEDACPEQALVERRPSRLRRGWLVGIA ATLLALAGGLGAAGYFALRSHQESQSIAREDLAAIEAAKDCVAATQAPDAGAMSASMQKI IECGTGDFGAQASLYTSMLVEAYQAASVHVQVTDMRAAVERNNNDGSVDVLVALRVKVSN TDSDAHEVGYRLRVRMALDEGRYKIAKLDQVTK
experiment.sample.molecule[0].mw14.807
experiment.sample.molecule[0].total_mw59.228
experiment.sample.molecule[0].number_molecules4
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionMam1A/Rv0175 delta 106 is N-terminally truncated construct which lacks the alpha1-helix. Protein, despite the removal of TM-helix, is not soluble and required C12E9 detergent to be solubilized. Tetrameric form was calculated with SEC-MALS.
experiment.sample.buffer.name50 mM Tris, 500 mM NaCl, D-C12E9
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.comment50mM Tris at pH8.5 with 500mM NaCl, supplemented with 0.003% Deuterated C12E9
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph8.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameProbable conserved Mce associated membrane protein (Mam1Adelta106) from M.tuberculosis (SANS)
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 Helsinki
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameMikko
experiment.contributor[0].contributor_surnameHynönen
experiment.contributor[0].orcidhttps://orcid.org/0000-0003-2431-8892
experiment.contributor[1].affiliation[0].short_namenull
experiment.contributor[1].affiliation[0].addressFinland
experiment.contributor[1].affiliation[0].full_nameUniversity of Oulu
experiment.contributor[1].affiliation[0].webpagehttps://www.oulu.fi
experiment.contributor[1].contributor_nameRajaram
experiment.contributor[1].contributor_surnameVenkatesan
experiment.contributor[1].orcidhttps://orcid.org/0000-0002-7257-1211
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2024-04-25
experiment.storage_temperature4.0
experiment.cell_temperature6.0
experiment.exposure_timenull
experiment.number_of_framesnull
experiment.wavelengthnull
experiment.sample_detector_distancenull
experiment.concentration_minnull
experiment.concentration_maxnull
experiment.sample_volume35.0
experiment.flow_rate0.07
experiment.s_min0.062
experiment.s_max7.827
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].models[0].softwareAlphaFold
fits[0].models[0].pdb_link[]
fits[0].models[0].model_title1A_107_Main_Model_Tetra_SASDXG2
fits[0].models[0].type_of_modelatomic
fits[0].models[0].software_versionnull
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fits[0].models[0].model_mw59.49
fits[0].models[0].bead_radius1.9
fits[0].models[0].lognull
fits[0].models[0].symmetrynull
fits[0].models[0].commentnull
fits[0].models[0].user1328
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fits[0].softwareCRYSON
fits[0].chi_square_value2.58
fits[0].p_value0.0272
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fits[0].software_versionnull
fits[0].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionSANS data were collected on the Zoom time-of-flight SANS instrument (ISIS Neutron and Muon Source, Harwell, UK) using wavelength range 1.75-16.5Å. The source to sample and sample to detector distance was 4 m and the beam size was 12 mm. Mam1Adelta106 was solubilized with C12E9 in the lysis buffer where the deuteration of the C12E9 was 0.2 % v/v. Excess C12E9 was washed away throughout the purification, and replaced with D-C12E9 in the STFC SANS facilities using SEC Superdex200 column. From the highest point of the peak, 3 fractions were selected. Each of these fractions was loaded to Starna Scientific quartz round cuvette (match code 6,path length 1, type 32/Q/1), and SANS data were collected from each fraction with an exposure time of 1 h in 5 cycles (5 h total exposure time for each fraction). The neutron momentum transfer (q) standard deviation and truncated scattering data are provided as an additional file.
experiment_descriptionnull
tags[]
intensity_unitarbitrary
experimental_mw33.1
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw20.0
porod_mw_errornull
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guinier_i0_errornull
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pddf_rg_errornull
guinier_rg2.553
guinier_rg_error0.683
pddf_dmax8.5
pddf_dmax_errornull
porod_volume70.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first17
guinier_point_last28
pddf_point_first18
pddf_point_last44
i0_calibration_standard_datanull
intensities_log_log_plotSASDXG2_datloglog_img.png
symmetrynull
last_modified2026-05-05T11:41:40.417306+02:00
bragg_peak[]
manifest.json:34 个字段值
字段路径原始值
codeSASDXG2
statussuccess
started_at2026-08-11T13:38:37.444224+00:00
finished_at2026-08-11T13:38:44.321680+00:00
source_last_modified2026-05-05T11:41:40.417306+02:00
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查看完整 summary.json 原文
{
  "code": "SASDXG2",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Insight into the structure and interactions of the <i>M. tuberculosis</i>\n            Mce-associated membrane proteins Mam1A-1D",
    "publication": {
      "title": "Insight into the structure and interactions of the <i>M. tuberculosis</i>\n            Mce-associated membrane proteins Mam1A-1D",
      "author_list": "Hynönen M, Perumal P, Hynönen N, Doutch J, Ma K, Venkatesan R",
      "journal": null,
      "doi": "10.1101/2025.03.26.645568",
      "pmid": null,
      "published_date": "2025 Mar 26"
    },
    "status": "released",
    "submitted_date": "2025-03-26",
    "released_date": "2025-04-11"
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          "long_name": "Probable conserved Mce associated membrane protein",
          "short_name": "Mam1A delta 106",
          "sequence": "MKHHHHHHPMSDYDIPTTENLYFQGAMAPDAGAMSASMQKIIECGTGDFGAQASLYTSMLVEAYQAASVHVQVTDMRAAVERNNNDGSVDVLVALRVKVSNTDSDAHEVGYRLRVRMALDEGRYKIAKLDQVTK",
          "organism": "Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv)",
          "uniprot_code": "O07419",
          "uniprot_range_first": 107,
          "uniprot_range_last": 213,
          "oligomerization": "tetramer",
          "molecular_type": "protein",
          "uniprot_sequence": "MKAADSAESDAGADQTGPQVKAADSAESDAGELGEDACPEQALVERRPSRLRRGWLVGIA\nATLLALAGGLGAAGYFALRSHQESQSIAREDLAAIEAAKDCVAATQAPDAGAMSASMQKI\nIECGTGDFGAQASLYTSMLVEAYQAASVHVQVTDMRAAVERNNNDGSVDVLVALRVKVSN\nTDSDAHEVGYRLRVRMALDEGRYKIAKLDQVTK",
          "mw": 14.807,
          "total_mw": 59.228,
          "number_molecules": 4,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": "Mam1A/Rv0175 delta 106 is N-terminally truncated construct which lacks the alpha1-helix. Protein, despite the removal of TM-helix, is not soluble and required C12E9 detergent to be solubilized. Tetrameric form was calculated with SEC-MALS."
        }
      ],
      "buffer": {
        "name": "50 mM Tris, 500 mM NaCl, D-C12E9",
        "concentration_unit": null,
        "comment": "50mM Tris at pH8.5 with 500mM NaCl, supplemented with 0.003% Deuterated C12E9",
        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 8.5,
        "deuteration": null
      },
      "purity_method": null,
      "name": "Probable conserved Mce associated membrane protein (Mam1Adelta106) from M.tuberculosis (SANS)",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": null,
            "address": null,
            "full_name": "University of Helsinki",
            "webpage": null
          }
        ],
        "contributor_name": "Mikko",
        "contributor_surname": "Hynönen",
        "orcid": "https://orcid.org/0000-0003-2431-8892"
      },
      {
        "affiliation": [
          {
            "short_name": null,
            "address": "Finland",
            "full_name": "University of Oulu",
            "webpage": "https://www.oulu.fi"
          }
        ],
        "contributor_name": "Rajaram",
        "contributor_surname": "Venkatesan",
        "orcid": "https://orcid.org/0000-0002-7257-1211"
      }
    ],
    "concentration_method": null,
    "concentration_unit": null,
    "date": "2024-04-25",
    "storage_temperature": 4.0,
    "cell_temperature": 6.0,
    "exposure_time": null,
    "number_of_frames": null,
    "wavelength": null,
    "sample_detector_distance": null,
    "concentration_min": null,
    "concentration_max": null,
    "sample_volume": 35.0,
    "flow_rate": 0.07,
    "s_min": 0.062,
    "s_max": 7.827,
    "total_exposure_time": null,
    "seccolumn": null
  },
  "fits": [
    {
      "models": [
        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/1A_107_Main_Model_Tetra_img.png",
          "software": "AlphaFold",
          "pdb_link": [],
          "model_title": "1A_107_Main_Model_Tetra_SASDXG2",
          "type_of_model": "atomic",
          "software_version": null,
          "model_data": "https://www.sasbdb.org/media/pdb_file/1A_107_Main_Model_Tetra.pdb",
          "model_mw": 59.49,
          "bead_radius": 1.9,
          "log": null,
          "symmetry": null,
          "comment": null,
          "user": 1328
        }
      ],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDXG2_fit1_fixed_fit_img.png",
      "software": "CRYSON",
      "chi_square_value": 2.58,
      "p_value": 0.0272,
      "fit_residual_plot": "SASDXG2_fit1_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDXG2_fit1.fit",
      "fit_log": "https://www.sasbdb.org/media/fitting_files/log_files/SASDXG2_1A_107_Main_Model_Cryson_3Bcycig.log",
      "software_version": null,
      "description": ""
    }
  ],
  "estimated_volume_method": null,
  "pddf_software": "ATSAS GNOM",
  "pddf_software_version": "5.0",
  "i0_calibration_standard": null,
  "description": "SANS data were collected on the Zoom time-of-flight SANS instrument (ISIS Neutron and Muon Source, Harwell, UK) using wavelength range 1.75-16.5Å. The source to sample and sample to detector distance was 4 m and the beam size was 12 mm. Mam1Adelta106 was solubilized with C12E9 in the lysis buffer where the deuteration of the C12E9 was 0.2 % v/v. Excess C12E9 was washed away throughout the purification, and replaced with D-C12E9 in the STFC SANS facilities using SEC Superdex200 column.  From the highest point of the peak, 3 fractions were selected. Each of these fractions was loaded to Starna Scientific quartz round cuvette (match code 6,path length 1, type 32/Q/1), and SANS data were collected from each fraction with an exposure time of 1 h in 5 cycles (5 h total exposure time for each fraction). The neutron momentum transfer (q) standard deviation and truncated scattering data are provided as an additional file.",
  "experiment_description": null,
  "tags": [],
  "intensity_unit": "arbitrary",
  "experimental_mw": 33.1,
  "experimental_mw_error": null,
  "guinier_i0_mw": null,
  "guinier_i0_mw_error": null,
  "porod_mw": 20.0,
  "porod_mw_error": null,
  "pddf_i0": 0.126,
  "pddf_i0_error": null,
  "guinier_i0": 0.124085,
  "guinier_i0_error": null,
  "pddf_rg": 2.58,
  "pddf_rg_error": null,
  "guinier_rg": 2.553,
  "guinier_rg_error": 0.683,
  "pddf_dmax": 8.5,
  "pddf_dmax_error": null,
  "porod_volume": 70.0,
  "porod_volume_error": null,
  "estimated_volume": null,
  "estimated_volume_error": null,
  "guinier_point_first": 17,
  "guinier_point_last": 28,
  "pddf_point_first": 18,
  "pddf_point_last": 44,
  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDXG2_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2026-05-05T11:41:40.417306+02:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
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  "started_at": "2026-08-11T13:38:37.444224+00:00",
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