SASDWM8

Tumbleweed protein composed of synthetic constructs TW1 and TW2 linked covalently via SpyTag/SpyCatcher

Data type: SASBDB experimental data Status: Published Curve type: Single concentration Last updated: 2026-07-07T15:34:42.237325+02:00

TW is a protein formed by covalent linkage of the the proteins TW1 and TW2 via a SpyTag/SpyCatcher. SAXS data was collected at the SAXS/WAXS beamline at the Australian Synchrotron, with Pilatus 2M detector at a SDD of 2680mm, with an incident intensity of ~8 x 10^12 ph/s. A SEC-SAXS setup with sheath flow was used. The running buffer was 10 mM HEPES pH 7.4, 150 mM NaCl, 5mM MgCl2, and 50uL of sample at ~10mg/mL was injected onto a Superdex 200 Increase 5/150 GL running at 0.2mL/min. Buffer scattering frames taken immediately before the void fraction. Sample scattering frames taken at the elution peak over a region of stable Rg using CHROMIX. Data were fit by a 2-state model using MultiFoXS.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Tumbleweed protein composed of synthetic constructs TW1 and TW2 linked covalently via SpyTag/SpyCatcher

Concentration— – 10.0 Buffer / pH10 mM HEPES, 150 mM NaCl, 5mM MgCl2 / 7.4
Experimental temperature20.0 Facility / beamlineAustralian Synchrotron / SAXS/WAXS
Wavelength0.10332 nmExposure1.0 s × 10

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Tumbleweed
View sequence
GKDLVDTTEMYLRTIYELEEEGVTPLRARIAERLEQSGPTVSQTVARMERDGLVVVASDRSLQMTPTGRTLATAVMRKHRLAERLLTDIIGLDINKVHDEADRWEHVMSDEVERRLVKVLKGSSGGSGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGGSGSSGDSATHIKFSKRDEDGKELAGATMELRDSSGKTISTWISDGQVKDFYLYPGKYTFVETAAPDGYEVATAITFTVNEQGQVTVNGKATKGDAHISGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGGSGSSGDSATHIKFSKRDEDGKELAGATMELRDSSGKTISTWISDGQVKDFYLYPGKYTFVETAAPDGYEVATAITFTVNEQGQVTVNGKATKGDAHIGAQQSPYSAAMAEQRHQEWLRFVDLLKNAYQNDLHLPLLNLMLTPDEREALGTRVRIVEELLRGEMSQRELKNELGAGIATITRGSNSLKAAPVELRQWLEEVLLKSDGSSGGSGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGGSGSSGAHIVMVDAYKPTKGSSGSGSSGAHIVMVDAYKPTKGSSGGSGSSGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGGSGGAEWSGEYISPYAEHGKKSEQVKKITVSIPLKVLKILTDERTRRKVNNLRHATNSELLCEAFLHAFTGQPLPDDADLRKERSDEIPEAAKEIMREMGINPETWEYSGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGSSGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGKDLVDTTEMYLRTIYELEEEGVTPLRARIAERLEQSGPTVSQTVARMERDGLVVVASDRSLQMTPTGRTLATAVMRKHRLAERLLTDIIGLDINKVHDEADRWEHVMSDEVERRLVKVLKGSSGAQQSPYSAAMAEQRHQEWLRFVDLLKNAYQNDLHLPLLNLMLTPDEREALGTRVRIVEELLRGEMSQRELKNELGAGIATITRGSNSLKAAPVELRQWLEEVLLKSDGSSSGGAEWSGEYISPYAEHGKKSEQVKKITVSIPLKVLKILTDERTRRKVNNLRHATNSELLCEAFLHAFTGQPLPDDADLRKERSDEIPEAAKEIMREMGINPETWEY
proteinsynthetic construct——–—monomerMolecule count 1132.785 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
11402[3]0.00470691–0.4919686 1/AHas uncertainty columnMissing 0107sasbdb/entries/m8/sasdwm8/source/SASDWM8.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)27.01.0Å
i0Guinier0.0613714—1/cm
i0P(r)0.061770.000151/cm
mwExperimental156.0—kDa
mwPorod156.0—kDa
porod_volumePorod190.0—ų
rgGuinier6.6590.266Å
rgP(r)6.910.04Å

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

▼

3. Source Fits and Models Source Fits & Models

Fit 1 · FoXS

χ²: 1.5624CorMap p: 0.1564Unit: 1/A

Ensemble fit composed of 2 conformations

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—atomicMultiFoXS —132.7—Model Image
▶

4. Source File Index Source Files

▶

5. Experiment Description and Publication Experiment & Publication

▼

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 name10 mM HEPES, 150 mM NaCl, 5mM MgCl2Buffer concentration—
pH7.4Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2023-03-15Storage / measurement temperature10.0 / 20.0
Exposure time1.0Frames10
Wavelength0.10332Sample-to-detector distance2.68
SourceX-ray synchrotronDetectorPilatus3 S 2M
Facility / beamlineAustralian Synchrotron / SAXS/WAXS · Melbourne, Australia
q range0.047 – 4.92Sample 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:179 field values
Field pathRaw value
codeSASDWM8
statusPublished
type_of_curveSingle concentration
angular_unit1/A
project.titleClocked stepping of an artificial protein walker along a DNA track.
project.publication.titleClocked stepping of an artificial protein walker along a DNA track.
project.publication.author_listNilsson P, Robertson NO, Gustafsson N, Davies RB, Liew CW, Lyons A, Eichhorn R, Niman CS, Blab GA, Bromley EHC, Whitten AE, Duff AP, Unksov IN, Beech JP, Jönsson P, Böcking T, Höcker B, Woolfson DN, Forde NR, Linke H, Curmi PMG
project.publication.journalNat Nanotechnol
project.publication.doi10.1038/s41565-026-02211-3
project.publication.pmid42410215
project.publication.published_date2026 Jul 6
project.statusreleased
project.submitted_date2025-02-20
project.released_date2026-02-20
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDWM8.out
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intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDWM8_dat_img.png
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sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDWM8.sascif
experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus3 S 2M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameAustralian Synchrotron
experiment.instrument.cityMelbourne
experiment.instrument.countryAustralia
experiment.instrument.beamline_nameSAXS/WAXS
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_nameTumbleweed
experiment.sample.molecule[0].short_nameTW
experiment.sample.molecule[0].sequenceGKDLVDTTEMYLRTIYELEEEGVTPLRARIAERLEQSGPTVSQTVARMERDGLVVVASDRSLQMTPTGRTLATAVMRKHRLAERLLTDIIGLDINKVHDEADRWEHVMSDEVERRLVKVLKGSSGG SGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGGSGSSGDSATHIKFSKRDEDGKELAGATMELRDSSGKTISTWISDGQVKDFYLYPGKYTFVETAAPDGYEVATAITFTVNEQGQVTVNGKATKGDAHISGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGGSGSSGDSATHIKFSKRDEDGKELAGATMELRDSSGKTISTWISDGQVKDFYLYPGKYTFVETAAPDGYEVATAITFTVNEQGQVTVNGKATKGDAHI GAQQSPYSAAMAEQRHQEWLRFVDLLKNAYQNDLHLPLLNLMLTPDEREALGTRVRIVEELLRGEMSQRELKNELGAGIATITRGSNSLKAAPVELRQWLEEVLLKSDGSSGGSGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGGSGSSGAHIVMVDAYKPTKGSSG SGSSGAHIVMVDAYKPTKGSSGGSGSSGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSSGGSGGAEWSGEYISPYAEHGKKSEQVKKITVSIPLKVLKILTDERTRRKVNNLRHATNSELLCEAFLHAFTGQPLPDDADLRKERSDEIPEAAKEIMREMGINPETWEY SGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSS GSSGTLYEALKENEKLHKEIEQKDNEIARLKKENKELAEVAQGSS GKDLVDTTEMYLRTIYELEEEGVTPLRARIAERLEQSGPTVSQTVARMERDGLVVVASDRSLQMTPTGRTLATAVMRKHRLAERLLTDIIGLDINKVHDEADRWEHVMSDEVERRLVKVLKGSS GAQQSPYSAAMAEQRHQEWLRFVDLLKNAYQNDLHLPLLNLMLTPDEREALGTRVRIVEELLRGEMSQRELKNELGAGIATITRGSNSLKAAPVELRQWLEEVLLKSDGSS SGGAEWSGEYISPYAEHGKKSEQVKKITVSIPLKVLKILTDERTRRKVNNLRHATNSELLCEAFLHAFTGQPLPDDADLRKERSDEIPEAAKEIMREMGINPETWEY
experiment.sample.molecule[0].organismsynthetic construct
experiment.sample.molecule[0].uniprot_codenull
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequence
experiment.sample.molecule[0].mw132.785
experiment.sample.molecule[0].total_mw132.785
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_descriptionTW protein composed of constructs TW1 and TW2 linked covalently via SpyTag/SpyCatcher
experiment.sample.buffer.name10 mM HEPES, 150 mM NaCl, 5mM MgCl2
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.nameTumbleweed protein composed of synthetic constructs TW1 and TW2 linked covalently via SpyTag/SpyCatcher
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_nameANSTO
experiment.contributor[0].affiliation[0].addressKirrawee DC, NSW 2232, Australia
experiment.contributor[0].affiliation[0].full_nameAustralian Nuclear Science and Technology Organisation
experiment.contributor[0].affiliation[0].webpage
experiment.contributor[0].contributor_nameAndrew
experiment.contributor[0].contributor_surnameWhitten
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2023-03-15
experiment.storage_temperature10.0
experiment.cell_temperature20.0
experiment.exposure_time1.0
experiment.number_of_frames10
experiment.wavelength0.10332
experiment.sample_detector_distance2.68
experiment.concentration_minnull
experiment.concentration_max10.0
experiment.sample_volumenull
experiment.flow_ratenull
experiment.s_min0.047
experiment.s_max4.92
experiment.total_exposure_timenull
experiment.seccolumnnull
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fits[0].models[0].softwareMultiFoXS
fits[0].models[0].pdb_link[]
fits[0].models[0].model_titlenull
fits[0].models[0].type_of_modelatomic
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fits[0].models[0].bead_radiusnull
fits[0].models[0].lognull
fits[0].models[0].symmetrynull
fits[0].models[0].comment72.5% of ensemble
fits[0].models[0].user111
fits[0].fit_unit1/A
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fits[0].softwareFoXS
fits[0].chi_square_value1.5624
fits[0].p_value0.1564
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fits[1].models[0].softwareMultiFoXS
fits[1].models[0].pdb_link[]
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
fits[1].models[0].lognull
fits[1].models[0].symmetrynull
fits[1].models[0].comment27.5% of ensemble
fits[1].models[0].user111
fits[1].fit_unit1/A
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fits[1].softwareFoXS
fits[1].chi_square_value1.5624
fits[1].p_value0.1564
fits[1].fit_residual_plotSASDWM8_fit2_fitresiduals_img.png
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fits[1].fit_lognull
fits[1].software_versionnull
fits[1].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version4.6
i0_calibration_standardnull
descriptionTW is a protein formed by covalent linkage of the the proteins TW1 and TW2 via a SpyTag/SpyCatcher. SAXS data was collected at the SAXS/WAXS beamline at the Australian Synchrotron, with Pilatus 2M detector at a SDD of 2680mm, with an incident intensity of ~8 x 10^12 ph/s. A SEC-SAXS setup with sheath flow was used. The running buffer was 10 mM HEPES pH 7.4, 150 mM NaCl, 5mM MgCl2, and 50uL of sample at ~10mg/mL was injected onto a Superdex 200 Increase 5/150 GL running at 0.2mL/min. Buffer scattering frames taken immediately before the void fraction. Sample scattering frames taken at the elution peak over a region of stable Rg using CHROMIX. Data were fit by a 2-state model using MultiFoXS.
experiment_descriptionnull
tags[]
intensity_unit1/cm
experimental_mw156.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw156.0
porod_mw_errornull
pddf_i00.06177
pddf_i0_error0.00015
guinier_i00.0613714
guinier_i0_errornull
pddf_rg6.91
pddf_rg_error0.04
guinier_rg6.659
guinier_rg_error0.266
pddf_dmax27.0
pddf_dmax_error1.0
porod_volume190.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first4
guinier_point_last41
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDWM8_datloglog_img.png
symmetrynull
last_modified2026-07-07T15:34:42.237325+02:00
bragg_peak[]
manifest.json:34 field values
Field pathRaw value
codeSASDWM8
statussuccess
started_at2026-08-11T15:56:48.706497+00:00
finished_at2026-08-11T15:56:57.690637+00:00
source_last_modified2026-07-07T15:34:42.237325+02:00
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View the complete summary.json source
{
  "code": "SASDWM8",
  "status": "Published",
  "type_of_curve": "Single concentration",
  "angular_unit": "1/A",
  "project": {
    "title": "Clocked stepping of an artificial protein walker along a DNA track.",
    "publication": {
      "title": "Clocked stepping of an artificial protein walker along a DNA track.",
      "author_list": "Nilsson P, Robertson NO, Gustafsson N, Davies RB, Liew CW, Lyons A, Eichhorn R, Niman CS, Blab GA, Bromley EHC, Whitten AE, Duff AP, Unksov IN, Beech JP, Jönsson P, Böcking T, Höcker B, Woolfson DN, Forde NR, Linke H, Curmi PMG",
      "journal": "Nat Nanotechnol",
      "doi": "10.1038/s41565-026-02211-3",
      "pmid": "42410215",
      "published_date": "2026 Jul 6"
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}
View the complete manifest.json source
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