SASDF63

Bruton's Tyrosine Kinase - SH2-kinase domain

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2020-08-28T15:27:49.639423+02:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Bruton's Tyrosine Kinase - SH2-kinase domain

Concentration— – 20.4 Buffer / pH20mM Tris, 150mM NaCl, 1mM TCEP, 5% glycerol / 7.5
Experimental temperature10.0 Facility / beamlineESRF / BM29
Wavelength0.09919 nmExposure2100.0 s × 2100

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Bruton's tyrosine kinase - Src homolgy domain 2 - kinase domain
View sequence
GAMGSMTEAEDSIEMYEWYSKHMTRSQAEQLLKQEGKEGGFIVRDSSKAGKYTVSVFAKSTGDPQGVIRHYVVCSTPQSQYYLAEKHLFSTIPELINYHQHNSAGLISRLKYPVSQQNKNAPSTAGLGYGSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEFIEEAKVMMNLSHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMCKDVCEAMEYLESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVRWSPPEVLMYSKFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLASEKVYTIMYSCWHEKADERPTFKILLSNILDVMDEES
proteinHomo sapiens—270–659monomerMolecule count 145.519 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11038[3]0.05892963–4.94623 1/nmHas uncertainty columnMissing 039sasbdb/entries/63/sasdf63/source/SASDF63.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)9.4—nm
i0Guinier85.10.13—
i0P(r)85.59——
mwExperimental46.65—kDa
mwPorod40.0—kDa
porod_volumePorod64.47—nm³
rgGuinier2.80.01nm
rgP(r)2.872—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

Fit 1 · DAMMIN

χ²: 1.119CorMap p: 0.237315Unit: 1/A

Ab initio envelope reconstruction of human Btk SH2-KD.

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—dummyDAMMIN —39.093—Model Image Log

Fit 2 · EOM/GAJOE

χ²: 1.414CorMap p: 0.007601Unit: 1/A

EOM analysis of human Btk SH2-KD using SH2 and KD structures as input (PDB 2GE9 and 1K2P).

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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 name20mM Tris, 150mM NaCl, 1mM TCEP, 5% glycerolBuffer concentration—
pH7.5Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2018-11-03Storage / measurement temperature10.0 / 10.0
Exposure time2100.0Frames2100
Wavelength0.09919Sample-to-detector distance2.869
SourceX-ray synchrotronDetectorPilatus 1M
Facility / beamlineESRF / BM29 · Grenoble, France
q range0.059 – 4.946Sample 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:167 field values
Field pathRaw value
codeSASDF63
statusPublished
type_of_curveSEC-SAS
angular_unit1/nm
project.titleBtk SH2-kinase interface is critical for allosteric kinase activation and its targeting inhibits B-cell neoplasms
project.publication.titleBtk SH2-kinase interface is critical for allosteric kinase activation and its targeting inhibits B-cell neoplasms
project.publication.author_listDuarte D, Lamontanara A, La Sala G, Jeong S, Sohn Y, Panjkovich A, Georgeon S, Kükenshöner T, Marcaida M, Pojer F, De Vivo M, Svergun D, Kim H, Dal Peraro M, Hantschel O
project.publication.journalNature Communications
project.publication.doi10.1038/s41467-020-16128-5
project.publication.pmidnull
project.publication.published_date2020 May 8
project.statusreleased
project.submitted_date2019-02-20
project.released_date2020-01-08
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDF63.out
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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_nameBruton's tyrosine kinase - Src homolgy domain 2 - kinase domain
experiment.sample.molecule[0].short_namehBtk - SH2-KD
experiment.sample.molecule[0].sequenceGAMGSMTEAEDSIEMYEWYSKHMTRSQAEQLLKQEGKEGGFIVRDSSKAGKYTVSVFAKSTGDPQGVIRHYVVCSTPQSQYYLAEKHLFSTIPELINYHQHNSAGLISRLKYPVSQQNKNAPSTAGLGYGSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEFIEEAKVMMNLSHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMCKDVCEAMEYLESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVRWSPPEVLMYSKFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLASEKVYTIMYSCWHEKADERPTFKILLSNILDVMDEES
experiment.sample.molecule[0].organismHomo sapiens
experiment.sample.molecule[0].uniprot_codenull
experiment.sample.molecule[0].uniprot_range_first270
experiment.sample.molecule[0].uniprot_range_last659
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequencenull
experiment.sample.molecule[0].mw45.519
experiment.sample.molecule[0].total_mw45.519
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.name20mM Tris, 150mM NaCl, 1mM TCEP, 5% glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
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experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameBruton's Tyrosine Kinase - SH2-kinase domain
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].addressSwitzerland
experiment.contributor[0].affiliation[0].full_nameÉcole polytechnique fédérale de Lausanne (EPFL)
experiment.contributor[0].affiliation[0].webpagehttps://www.epfl.ch
experiment.contributor[0].contributor_nameDaniel
experiment.contributor[0].contributor_surnameDuarte
experiment.contributor[0].orcidhttps://orcid.org/0000-0001-6730-7582
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2018-11-03
experiment.storage_temperature10.0
experiment.cell_temperature10.0
experiment.exposure_time2100.0
experiment.number_of_frames2100
experiment.wavelength0.09919
experiment.sample_detector_distance2.869
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experiment.concentration_max20.4
experiment.sample_volumenull
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experiment.s_min0.059
experiment.s_max4.946
experiment.total_exposure_timenull
experiment.seccolumnnull
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDF63_fit1_model1_img.png
fits[0].models[0].softwareDAMMIN
fits[0].models[0].pdb_link[]
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fits[0].models[0].bead_radius2.5
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fits[0].softwareDAMMIN
fits[0].chi_square_value1.119
fits[0].p_value0.237315
fits[0].fit_residual_plotSASDF63_fit1_fitresiduals_img.png
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fits[0].software_versionnull
fits[0].descriptionAb initio envelope reconstruction of human Btk SH2-KD.
fits[1].models[]
fits[1].fit_unit1/A
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fits[1].softwareEOM/GAJOE
fits[1].chi_square_value1.414
fits[1].p_value0.007601
fits[1].fit_residual_plotSASDF63_fit2_fitresiduals_img.png
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fits[1].software_versionnull
fits[1].descriptionEOM analysis of human Btk SH2-KD using SH2 and KD structures as input (PDB 2GE9 and 1K2P).
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data for SH2-kinase domain (amino acids 270-659) wild-type of human Bruton’s tyrosine kinase (Btk) in 20 mM Tris-HCl, 150 mM NaCl, 5% Glycerol, 1 mM TCEP, pH 7.5 were collected on the BM29 beam line at the ESRF (Grenoble, France) using a Dectris Pilatus 1M detector at a sample-detector distance of 2.849 m and at a wavelength of λ = 0.099 nm (l(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size exclusion chromatography (SEC) SAXS was performed by injecting 100µl of protein sample at 20mg/mL in a Superdex S200 Increase 10/300 column (GE Healthcare) at flow rate of 0.7mL/minute at room temperature. 2100 frames were collect during the 35 minutes total run. SEC-SAXS data frames 1031 - 1077 corresponding to monomeric peak were scaled, averaged and subtracted from an appropriate the solvent-blank to produce the final curve. The final scattering curve was analysed using PRIMUS software (ATSAS). The bead model depicts the DAMMIN ab initio reconstruction. Ensemble optimisation method (EOM) was performed using SH2 and kinase domain structures (2GE9 and 1K2P, PDB) to assess construct’s flexibility.
tags[]
intensity_unitnull
experimental_mw46.65
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw40.0
porod_mw_errornull
pddf_i085.59
pddf_i0_errornull
guinier_i085.1
guinier_i0_error0.13
pddf_rg2.872
pddf_rg_errornull
guinier_rg2.8
guinier_rg_error0.01
pddf_dmax9.4
pddf_dmax_errornull
porod_volume64.47
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first33
guinier_point_last86
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDF63_datloglog_img.png
symmetrynull
last_modified2020-08-28T15:27:49.639423+02:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDF63
statussuccess
started_at2026-08-11T13:53:19.931510+00:00
finished_at2026-08-11T13:53:29.188664+00:00
source_last_modified2020-08-28T15:27:49.639423+02:00
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View the complete summary.json source
{
  "code": "SASDF63",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/nm",
  "project": {
    "title": "Btk SH2-kinase interface is critical for allosteric kinase activation and its targeting inhibits B-cell neoplasms",
    "publication": {
      "title": "Btk SH2-kinase interface is critical for allosteric kinase activation and its targeting inhibits B-cell neoplasms",
      "author_list": "Duarte D, Lamontanara A, La Sala G, Jeong S, Sohn Y, Panjkovich A, Georgeon S, Kükenshöner T, Marcaida M, Pojer F, De Vivo M, Svergun D, Kim H, Dal Peraro M, Hantschel O",
      "journal": "Nature Communications",
      "doi": "10.1038/s41467-020-16128-5",
      "pmid": null,
      "published_date": "2020 May 8"
    },
    "status": "released",
    "submitted_date": "2019-02-20",
    "released_date": "2020-01-08"
  },
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        {
          "long_name": "Bruton's tyrosine kinase - Src homolgy domain 2 - kinase domain",
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            "short_name": null,
            "address": "Switzerland",
            "full_name": "École polytechnique fédérale de Lausanne (EPFL)",
            "webpage": "https://www.epfl.ch"
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View the complete manifest.json source
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