SASDWR5

Stimulatory element RNA

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2025-07-20T11:29:02.233366+02:00

The models displayed in this entry show: Top: A post normal-mode SREFLEX model obtained using an AlphaFold-predicted structure of the RNA as an initial template, and an alignment of several different SREFLEX outputs. Middle: a MONSA ab initio dummy-atom model reconstruction of the RNA particle. Bottom: A pseudoknot conformation based on the X-ray crystal structure of the RNA in complex with Protein 2A (refer to SASBDB entry SASDWS5; https://www.sasbdb.org/data/SASDWS5). The full entry archive contains the unsubtracted SEC-SAXS 1D-data frames in addition to DAMMIN, MONSA and SREFLEX modelling routines.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Stimulatory element RNA

Concentration— – 7.08 Buffer / pH20 mM HEPES pH 7.4, 400 mM KCl 2% v/v glycerol, 1 mM DTT / —
Experimental temperature20.0 Facility / beamlinePETRA III / EMBL P12
Wavelength0.123983 nmExposure0.25 s × 57

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Stimulatory element RNA
View sequence
CCACAAGGUGCGGUGCUAACUAAAUCCCUAGCACCCC
RNAsynthetic RNA——–—monomerMolecule count 111.836 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
12653[3]0.0255364–7.41322 1/nmHas uncertainty columnMissing 018sasbdb/entries/r5/sasdwr5/source/SASDWR5.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)8.0—nm
i0Guinier7530.62—arbitrary
i0P(r)7577.0—arbitrary
mwExperimental13.5—kDa
mwPorod10.0—kDa
porod_volumePorod18.9—nm³
rgGuinier1.9220.003nm
rgP(r)1.989—nm

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 · CRYSOL

χ²: 1.11CorMap p: 0.1916Unit: 1/A
ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—atomicSREFLEX —11.39—Model Image Log
2—otherOther [static image] ———Model
▶

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 name20 mM HEPES pH 7.4, 400 mM KCl 2% v/v glycerol, 1 mM DTTBuffer concentration—
pH—Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2021-04-26Storage / measurement temperature20.0 / 20.0
Exposure time0.25Frames57
Wavelength0.123983Sample-to-detector distance3.0
SourceX-ray synchrotronDetectorPilatus 6M
Facility / beamlinePETRA III / EMBL P12 · DESY; Hamburg, Germany
q range0.026 – 7.413Sample volume / flow rate50.0 / 0.35

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

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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:215 field values
Field pathRaw value
codeSASDWR5
statusPublished
type_of_curveSEC-SAS
angular_unit1/nm
project.titleA new protein-dependent riboswitch activates ribosomal frameshifting
project.publication.titleA new protein-dependent riboswitch activates ribosomal frameshifting
project.publication.author_listBetts J, Jeffries C, Passchier T, Kung H, Graham S, Abdelhamid M, Howard J, Craggs T, Graham S, Brierley I, Leake M, Quinn S, Hill C
project.publication.journalnull
project.publication.doi10.1101/2025.07.17.665365
project.publication.pmidnull
project.publication.published_date2025 Jul 18
project.statusreleased
project.submitted_date2025-04-01
project.released_date2025-07-20
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experiment.instrument.detector.resolutionnull
experiment.instrument.namePETRA III
experiment.instrument.cityDESY; Hamburg
experiment.instrument.countryGermany
experiment.instrument.beamline_nameEMBL P12
experiment.instrument.beam_geometrynull
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
experiment.instrument.line_collimationnull
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experiment.instrument.line_collimation_slitlengthnull
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experiment.instrument.xray_energynull
experiment.instrument.beam_profile_ahnull
experiment.instrument.beam_profile_alnull
experiment.sample.molecule[0].long_nameStimulatory element RNA
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceCCACAAGGUGCGGUGCUAACUAAAUCCCUAGCACCCC
experiment.sample.molecule[0].organismsynthetic RNA
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_typeRNA
experiment.sample.molecule[0].uniprot_sequence
experiment.sample.molecule[0].mw11.836
experiment.sample.molecule[0].total_mw11.836
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_descriptionSingle-stranded RNA
experiment.sample.buffer.name20 mM HEPES pH 7.4, 400 mM KCl 2% v/v glycerol, 1 mM DTT
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.phnull
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameStimulatory element RNA
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-Hamburg
experiment.contributor[0].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[0].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[0].contributor_nameCy M
experiment.contributor[0].contributor_surnameJeffries
experiment.contributor[0].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2021-04-26
experiment.storage_temperature20.0
experiment.cell_temperature20.0
experiment.exposure_time0.25
experiment.number_of_frames57
experiment.wavelength0.123983
experiment.sample_detector_distance3.0
experiment.concentration_minnull
experiment.concentration_max7.08
experiment.sample_volume50.0
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estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionThe models displayed in this entry show: Top: A post normal-mode SREFLEX model obtained using an AlphaFold-predicted structure of the RNA as an initial template, and an alignment of several different SREFLEX outputs. Middle: a MONSA ab initio dummy-atom model reconstruction of the RNA particle. Bottom: A pseudoknot conformation based on the X-ray crystal structure of the RNA in complex with Protein 2A (refer to SASBDB entry SASDWS5; https://www.sasbdb.org/data/SASDWS5). The full entry archive contains the unsubtracted SEC-SAXS 1D-data frames in addition to DAMMIN, MONSA and SREFLEX modelling routines.
experiment_descriptionSynchrotron SAXS data from solutions of stimulatory element RNA in 20 mM HEPES pH 7.4, 400 mM KCl 2% v/v glycerol, 1 mM DTT were collected on the EMBL P12 beam line at PETRA III (DESY; Hamburg, Germany) using a Pilatus 6M detector at a sample-detector distance of 3 m and at a wavelength of λ = 0.123983 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 50.00 μl sample at 7.1 mg/ml was injected at a 0.35 ml/min flow rate onto a GE Superdex 75 Increase 5/150 column at 20°C. 57 successive 0.250 second frames were collected through the SEC-elution peak. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[]
intensity_unitarbitrary
experimental_mw13.5
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw10.0
porod_mw_errornull
pddf_i07577.0
pddf_i0_errornull
guinier_i07530.62
guinier_i0_errornull
pddf_rg1.989
pddf_rg_errornull
guinier_rg1.922
guinier_rg_error0.003
pddf_dmax8.0
pddf_dmax_errornull
porod_volume18.9
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first49
guinier_point_last221
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDWR5_datloglog_img.png
symmetrynull
last_modified2025-07-20T11:29:02.233366+02:00
bragg_peak[]
manifest.json:34 field values
Field pathRaw value
codeSASDWR5
statussuccess
started_at2026-08-11T14:54:23.165683+00:00
finished_at2026-08-11T14:55:02.275440+00:00
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View the complete summary.json source
{
  "code": "SASDWR5",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/nm",
  "project": {
    "title": "A new protein-dependent riboswitch activates ribosomal frameshifting",
    "publication": {
      "title": "A new protein-dependent riboswitch activates ribosomal frameshifting",
      "author_list": "Betts J, Jeffries C, Passchier T, Kung H, Graham S, Abdelhamid M, Howard J, Craggs T, Graham S, Brierley I, Leake M, Quinn S, Hill C",
      "journal": null,
      "doi": "10.1101/2025.07.17.665365",
      "pmid": null,
      "published_date": "2025 Jul 18"
    },
    "status": "released",
    "submitted_date": "2025-04-01",
    "released_date": "2025-07-20"
  },
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            "address": "Notkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany",
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  "last_modified": "2025-07-20T11:29:02.233366+02:00",
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}
View the complete manifest.json source
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