SASDEF2

Mitochondrial import inner membrane translocase complex TIM9·10

Data type: SASBDB experimental data Status: Published Curve type: Merged Last updated: 2019-12-06T13:07:15.624532+01:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Mitochondrial import inner membrane translocase complex TIM9·10

Concentration1.0 – 5.0 Buffer / pH50mM Tris, 150mM NaCl / 7.4
Experimental temperature20.0 Facility / beamlineESRF / BM29
Wavelength0.099 nmExposure20.0 s × 1

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Mitochondrial import inner membrane translocase subunit TIM9
View sequence
MDALNSKEQQEFQKVVEQKQMKDFMRLYSNLVERCFTDCVNDFTTSKLTNKEQTCIMKCSEKFLKHSERVGQRFQEQNAALGQGLGR
proteinSaccharomyces cerevisiaeO74700—–—trimerMolecule count 310.202 kDa
Mitochondrial import inner membrane translocase subunit TIM10
View sequence
GSFLGFGGGQPQLSSQQKIQAAEAELDLVTDMFNKLVNNCYKKCINTSYSEGELNKNESSCLDRCVAKYFETNVQVGENMQKMGQSFNAAGKF
proteinSaccharomyces cerevisiaeP87108—–—trimerMolecule count 310.23 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11038[3]0.05988624–4.938935 1/nmHas uncertainty columnMissing 00sasbdb/entries/f2/sasdef2/source/SASDEF2.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)10.0—nm
i0Guinier49.970.03arbitrary
i0P(r)50.28—arbitrary
mwExperimental61.0—kDa
mwGuinier I(0)49.9710.0kDa
mwPorod61.0—kDa
porod_volumePorod103.0—nm³
rgGuinier2.670.01nm
rgP(r)2.725—nm

These values are reported by SASBDB; SAXSdb did not recalculate them from the experimental curve.

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3. Source Fits and Models Source Fits & Models

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4. Source File Index Source Files

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5. Experiment Description and Publication Experiment & Publication

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6. Complete Source Record Complete Source Record

The following content comes directly from the SASBDB entry. Missing values are shown as “—”; SAXSdb does not infer undeclared units.

Open the original SASBDB entry

Buffer and Sample Properties

Buffer name50mM Tris, 150mM NaClBuffer concentration—
pH7.4Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2015-08-27Storage / measurement temperature35.0 / 20.0
Exposure time20.0Frames1
Wavelength0.099Sample-to-detector distance2.864
SourceX-ray synchrotronDetectorPilatus 1M
Facility / beamlineESRF / BM29 · Grenoble, France
q range0.06 – 4.939Sample volume / flow rate— / —

Original SASBDB Plots

Experimental I(q)
Experimental I(q)
Experimental I(q), log-log
Experimental I(q), log-log
Guinier plot
Guinier plot
Kratky plot
Kratky plot
P(r) plot
P(r) plot

Downloadable Files

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All source fields (unfiltered)

Every source field is expanded here, including empty values, list members and fields already shown above.

summary.json:222 field values
Field pathRaw value
codeSASDEF2
statusPublished
type_of_curveMerged
angular_unit1/nm
project.titleStructural Basis of Membrane Protein Chaperoning through the Mitochondrial Intermembrane Space.
project.publication.titleStructural Basis of Membrane Protein Chaperoning through the Mitochondrial Intermembrane Space.
project.publication.author_listWeinhäupl K, Lindau C, Hessel A, Wang Y, Schütze C, Jores T, Melchionda L, Schönfisch B, Kalbacher H, Bersch B, Rapaport D, Brennich M, Lindorff-Larsen K, Wiedemann N, Schanda P
project.publication.journalCell
project.publication.doi10.1016/j.cell.2018.10.039
project.publication.pmid30445040
project.publication.published_date2018 Nov 15
project.statusreleased
project.submitted_date2018-08-13
project.released_date2018-11-21
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experiment.instrument.detector.typeDectris
experiment.instrument.detector.namePilatus 1M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameESRF
experiment.instrument.cityGrenoble
experiment.instrument.countryFrance
experiment.instrument.beamline_nameBM29
experiment.instrument.beam_geometry
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_nameMitochondrial import inner membrane translocase subunit TIM9
experiment.sample.molecule[0].short_nameTIM9
experiment.sample.molecule[0].sequenceMDALNSKEQQEFQKVVEQKQMKDFMRLYSNLVERCFTDCVNDFTTSKLTNKEQTCIMKCSEKFLKHSERVGQRFQEQNAALGQGLGR
experiment.sample.molecule[0].organismSaccharomyces cerevisiae
experiment.sample.molecule[0].uniprot_codeO74700
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationtrimer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMDALNSKEQQEFQKVVEQKQMKDFMRLYSNLVERCFTDCVNDFTTSKLTNKEQTCIMKCS EKFLKHSERVGQRFQEQNAALGQGLGR
experiment.sample.molecule[0].mw10.202
experiment.sample.molecule[0].total_mw30.606
experiment.sample.molecule[0].number_molecules3
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_nameMitochondrial import inner membrane translocase subunit TIM10
experiment.sample.molecule[1].short_namenull
experiment.sample.molecule[1].sequenceGSFLGFGGGQPQLSSQQKIQAAEAELDLVTDMFNKLVNNCYKKCINTSYSEGELNKNESSCLDRCVAKYFETNVQVGENMQKMGQSFNAAGKF
experiment.sample.molecule[1].organismSaccharomyces cerevisiae
experiment.sample.molecule[1].uniprot_codeP87108
experiment.sample.molecule[1].uniprot_range_firstnull
experiment.sample.molecule[1].uniprot_range_lastnull
experiment.sample.molecule[1].oligomerizationtrimer
experiment.sample.molecule[1].molecular_typeprotein
experiment.sample.molecule[1].uniprot_sequenceMSFLGFGGGQPQLSSQQKIQAAEAELDLVTDMFNKLVNNCYKKCINTSYSEGELNKNESS CLDRCVAKYFETNVQVGENMQKMGQSFNAAGKF
experiment.sample.molecule[1].mw10.23
experiment.sample.molecule[1].total_mw30.69
experiment.sample.molecule[1].number_molecules3
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.name50mM Tris, 150mM NaCl
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
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.nameMitochondrial import inner membrane translocase complex TIM9·10
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
experiment.contributor[0].affiliation[0].addressGrenoble, France
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Grenoble Outstation
experiment.contributor[0].affiliation[0].webpagehttps://www.embl.fr/
experiment.contributor[0].contributor_nameMartha
experiment.contributor[0].contributor_surnameBrennich
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2015-08-27
experiment.storage_temperature35.0
experiment.cell_temperature20.0
experiment.exposure_time20.0
experiment.number_of_frames1
experiment.wavelength0.099
experiment.sample_detector_distance2.864
experiment.concentration_min1.0
experiment.concentration_max5.0
experiment.sample_volumenull
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pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of the mitochondrial import inner membrane translocase complex (TIM9·10) in 50mM Tris, 150mM NaCl, pH 7.4 were collected on the BM29 beam line at the ESRF (Grenoble, France) using a Pilatus 1M detector at a sample-detector distance of 2.9 m and at a wavelength of λ = 0.099 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Solute concentrations ranging between 1 and 5 mg/ml were measured at 20°C. One 20 second frame was collected per concentration. 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 concentration were merged with the highest concentration high angle data to yield the final composite scattering curve.
tags[]
intensity_unitarbitrary
experimental_mw61.0
experimental_mw_errornull
guinier_i0_mw49.97
guinier_i0_mw_error10.0
porod_mw61.0
porod_mw_errornull
pddf_i050.28
pddf_i0_errornull
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pddf_rg2.725
pddf_rg_errornull
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pddf_dmax10.0
pddf_dmax_errornull
porod_volume103.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first7
guinier_point_last91
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDEF2_datloglog_img.png
symmetrynull
last_modified2019-12-06T13:07:15.624532+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDEF2
statussuccess
started_at2026-08-11T13:37:25.230308+00:00
finished_at2026-08-11T13:37:36.548963+00:00
source_last_modified2019-12-06T13:07:15.624532+01:00
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View the complete summary.json source
{
  "code": "SASDEF2",
  "status": "Published",
  "type_of_curve": "Merged",
  "angular_unit": "1/nm",
  "project": {
    "title": "Structural Basis of Membrane Protein Chaperoning through the Mitochondrial Intermembrane Space.",
    "publication": {
      "title": "Structural Basis of Membrane Protein Chaperoning through the Mitochondrial Intermembrane Space.",
      "author_list": "Weinhäupl K, Lindau C, Hessel A, Wang Y, Schütze C, Jores T, Melchionda L, Schönfisch B, Kalbacher H, Bersch B, Rapaport D, Brennich M, Lindorff-Larsen K, Wiedemann N, Schanda P",
      "journal": "Cell",
      "doi": "10.1016/j.cell.2018.10.039",
      "pmid": "30445040",
      "published_date": "2018 Nov 15"
    },
    "status": "released",
    "submitted_date": "2018-08-13",
    "released_date": "2018-11-21"
  },
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View the complete manifest.json source
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