SASDF53

Bruton's Tyrosine Kinase - kinase domain

Data type: SASBDB experimental data Status: Published Curve type: Merged Last updated: 2020-01-08T13:58:38.363103+01:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Bruton's Tyrosine Kinase - kinase domain

Concentration0.91 – 4.15 Buffer / pH20mM Tris, 150mM NaCl, 1mM TCEP, 5% glycerol / 7.5
Experimental temperature20.0 Facility / beamlineESRF / BM29
Wavelength0.09919 nmExposure1.0 s × 10

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Bruton's tyrosine kinase, kinase domain
View sequence
GAMGSGYGSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEFIEEAKVMMNLSHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMCKDVCEAMEYLESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVRWSPPEVLMYSKFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLASEKVYTIMYSCWHEKADERPTFKILLSNILDVMDEES
proteinHomo sapiensQ06187391–659monomerMolecule count 131.793 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11038[3]0.05816229–4.927701 1/nmHas uncertainty columnMissing 05sasbdb/entries/53/sasdf53/source/SASDF53.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)6.75—nm
i0Guinier24.980.034—
i0P(r)24.94——
mwExperimental28.9—kDa
mwPorod30.0—kDa
porod_volumePorod52.07—nm³
rgGuinier2.090.02nm
rgP(r)2.096—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: 1.002CorMap p: 0.092064Unit: 1/A

Bruton's tyrosine kinase - kinase domain ab initio bead model generated by DAMMIN (Online ATSAS)

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—dummyDAMMIN P125.418—Model Image Log
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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 date2018-05-11Storage / measurement temperature10.0 / 20.0
Exposure time1.0Frames10
Wavelength0.09919Sample-to-detector distance2.869
SourceX-ray synchrotronDetectorPilatus 1M
Facility / beamlineESRF / BM29 · Grenoble, France
q range0.058 – 4.928Sample 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:182 field values
Field pathRaw value
codeSASDF53
statusPublished
type_of_curveMerged
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
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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, kinase domain
experiment.sample.molecule[0].short_nameBtk-KD
experiment.sample.molecule[0].sequenceGAMGSGYGSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEFIEEAKVMMNLSHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMCKDVCEAMEYLESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVRWSPPEVLMYSKFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLASEKVYTIMYSCWHEKADERPTFKILLSNILDVMDEES
experiment.sample.molecule[0].organismHomo sapiens
experiment.sample.molecule[0].uniprot_codeQ06187
experiment.sample.molecule[0].uniprot_range_first391
experiment.sample.molecule[0].uniprot_range_last659
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMAAVILESIFLKRSQQKKKTSPLNFKKRLFLLTVHKLSYYEYDFERGRRGSKKGSIDVEK ITCVETVVPEKNPPPERQIPRRGEESSEMEQISIIERFPYPFQVVYDEGPLYVFSPTEEL RKRWIHQLKNVIRYNSDLVQKYHPCFWIDGQYLCCSQTAKNAMGCQILENRNGSLKPGSS HRKTKKPLPPTPEEDQILKKPLPPEPAAAPVSTSELKKVVALYDYMPMNANDLQLRKGDE YFILEESNLPWWRARDKNGQEGYIPSNYVTEAEDSIEMYEWYSKHMTRSQAEQLLKQEGK EGGFIVRDSSKAGKYTVSVFAKSTGDPQGVIRHYVVCSTPQSQYYLAEKHLFSTIPELIN YHQHNSAGLISRLKYPVSQQNKNAPSTAGLGYGSWEIDPKDLTFLKELGTGQFGVVKYGK WRGQYDVAIKMIKEGSMSEDEFIEEAKVMMNLSHEKLVQLYGVCTKQRPIFIITEYMANG CLLNYLREMRHRFQTQQLLEMCKDVCEAMEYLESKQFLHRDLAARNCLVNDQGVVKVSDF GLSRYVLDDEYTSSVGSKFPVRWSPPEVLMYSKFSSKSDIWAFGVLMWEIYSLGKMPYER FTNSETAEHIAQGLRLYRPHLASEKVYTIMYSCWHEKADERPTFKILLSNILDVMDEES
experiment.sample.molecule[0].mw31.793
experiment.sample.molecule[0].total_mw31.793
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
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.5
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameBruton's Tyrosine Kinase - 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.date2018-05-11
experiment.storage_temperature10.0
experiment.cell_temperature20.0
experiment.exposure_time1.0
experiment.number_of_frames10
experiment.wavelength0.09919
experiment.sample_detector_distance2.869
experiment.concentration_min0.91
experiment.concentration_max4.15
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.058
experiment.s_max4.928
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].models[0].bead_radius1.7
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fits[0].models[0].commentnull
fits[0].models[0].user406
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fits[0].softwareDAMMIN
fits[0].chi_square_value1.002
fits[0].p_value0.092064
fits[0].fit_residual_plotSASDF53_fit1_fitresiduals_img.png
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fits[0].software_versionnull
fits[0].descriptionBruton's tyrosine kinase - kinase domain ab initio bead model generated by DAMMIN (Online ATSAS)
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fits[1].models[0].softwarePDB (Protein Data Bank)
fits[1].models[0].pdb_link[0].pdb_code1k2p
fits[1].models[0].pdb_link[0].ext_code1K2P
fits[1].models[0].pdb_link[0].ext_typepdb
fits[1].models[0].pdb_link[0].difference_with_modelidentical
fits[1].models[0].model_titlenull
fits[1].models[0].type_of_modelatomic
fits[1].models[0].software_versionnull
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fits[1].models[0].bead_radiusnull
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fits[1].models[0].symmetrynull
fits[1].models[0].commentnull
fits[1].models[0].user406
fits[1].fit_unit1/A
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fits[1].softwareCRYSOL
fits[1].chi_square_value1.275
fits[1].p_value0.0
fits[1].fit_residual_plotSASDF53_fit2_fitresiduals_img.png
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fits[1].software_versionnull
fits[1].descriptionCRYSOL fitting to PDB 1k2p crystal structure.
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data for kinase domain (amino acids 391-659) 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). Solute concentrations ranging between 0.91 and 4.15 mg/ml were measured at 10°C. 10 successive 0.5 second frames were collected. 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. The final scattering curve was analysed using PRIMUS software (ATSAS). The model depicts the DAMMIN ab initio reconstruction superimposed with the crystal structure 1K2P (PDB).
tags[]
intensity_unitnull
experimental_mw28.9
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw30.0
porod_mw_errornull
pddf_i024.94
pddf_i0_errornull
guinier_i024.98
guinier_i0_error0.034
pddf_rg2.096
pddf_rg_errornull
guinier_rg2.09
guinier_rg_error0.02
pddf_dmax6.75
pddf_dmax_errornull
porod_volume52.07
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first3
guinier_point_last120
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDF53_datloglog_img.png
symmetrynull
last_modified2020-01-08T13:58:38.363103+01:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDF53
statussuccess
started_at2026-08-11T13:52:48.074940+00:00
finished_at2026-08-11T13:53:01.679626+00:00
source_last_modified2020-01-08T13:58:38.363103+01:00
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View the complete summary.json source
{
  "code": "SASDF53",
  "status": "Published",
  "type_of_curve": "Merged",
  "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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  "experiment": {
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        "name": "Pilatus 1M",
        "resolution": 172.0
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View the complete manifest.json source
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