SASDVZ4

ST9a RNA, PKmutant (59 nucleotides in 10 mM MgCl2; dimer)

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2025-09-01T15:31:28.121164+02:00
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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · ST9a RNA, PKmutant (59 nucleotides in 10 mM MgCl2; dimer)

Concentration— – 3.0 Buffer / pH50 mM Tris pH 7.5, 100 mM NaCl, 1 mM DTT, 10 mM MgCl2, 0.0002% w/v NaN3 / —
Experimental temperature20.0 Facility / beamlineNational Synchrotron Light Source II (NSLS-II) / 16-ID (LiX)
Wavelength0.082 nmExposure2.0 s × 1200

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
ST9 PKmutant (59 nt RNA)
View sequence
AAGUACCCUCCAAGCCCUACAGGUUGGAAGAGGGGGCUAUCAGUCCUGAUGGCAGACUC
RNA———–—dimerMolecule count 219.075 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
1200[3]0.06–10.0 1/nmHas uncertainty columnMissing 00sasbdb/entries/z4/sasdvz4/source/SASDVZ4.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)12.81—nm
i0Guinier10.2851—arbitrary
i0P(r)10.4—arbitrary
mwExperimental43.7—kDa
porod_volumePorod61.9—nm³
rgGuinier3.520.024nm
rgP(r)3.648—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

This entry has no source fit record.

▶

4. Source File Index Source Files

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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 name50 mM Tris pH 7.5, 100 mM NaCl, 1 mM DTT, 10 mM MgCl2, 0.0002% w/v NaN3Buffer concentration—
pH—Additives—
Buffer description10 mM MgCl2 buffer
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2024-01-30Storage / measurement temperature20.0 / 20.0
Exposure time2.0Frames1200
Wavelength0.082Sample-to-detector distance3.561
SourceX-ray synchrotronDetectorPilatus3 S 1M
Facility / beamlineNational Synchrotron Light Source II (NSLS-II) / 16-ID (LiX) · Upton, NY, USA
q range0.06 – 10.0Sample volume / flow rate95.0 / 0.75

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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summary:source record
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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:134 field values
Field pathRaw value
codeSASDVZ4
statusPublished
type_of_curveSEC-SAS
angular_unit1/nm
project.titleA conserved viral RNA fold enables nuclease resistance across kingdoms of life.
project.publication.titleA conserved viral RNA fold enables nuclease resistance across kingdoms of life.
project.publication.author_listGezelle JG, Korn SM, McDonald JT, Gong Z, Erickson A, Huang CH, Yang F, Cronin M, Kuo YW, Wimberly BT, Steckelberg AL
project.publication.journalNucleic Acids Res
project.publication.doi10.1093/nar/gkaf840
project.publication.pmid40884403
project.publication.published_date2025 Aug 27
project.statusreleased
project.submitted_date2024-07-12
project.released_date2025-07-12
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experiment.instrument.detector.resolution172.0
experiment.instrument.nameNational Synchrotron Light Source II (NSLS-II)
experiment.instrument.cityUpton, NY
experiment.instrument.countryUSA
experiment.instrument.beamline_name16-ID (LiX)
experiment.instrument.beam_geometrynull
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourceTrue
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_nameST9 PKmutant (59 nt RNA)
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceAAGUACCCUCCAAGCCCUACAGGUUGGAAGAGGGGGCUAUCAGUCCUGAUGGCAGACUC
experiment.sample.molecule[0].organismnull
experiment.sample.molecule[0].uniprot_codenull
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationdimer
experiment.sample.molecule[0].molecular_typeRNA
experiment.sample.molecule[0].uniprot_sequence
experiment.sample.molecule[0].mw19.075
experiment.sample.molecule[0].total_mw38.15
experiment.sample.molecule[0].number_molecules2
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_description
experiment.sample.buffer.name50 mM Tris pH 7.5, 100 mM NaCl, 1 mM DTT, 10 mM MgCl2, 0.0002% w/v NaN3
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.comment10 mM MgCl2 buffer
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.nameST9a RNA, PKmutant (59 nucleotides in 10 mM MgCl2; dimer)
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].addressnull
experiment.contributor[0].affiliation[0].full_nameColumbia University Irving Medical Center
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameSophie
experiment.contributor[0].contributor_surnameKorn
experiment.contributor[0].orcidhttps://orcid.org/0000-0003-3798-3277
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2024-01-30
experiment.storage_temperature20.0
experiment.cell_temperature20.0
experiment.exposure_time2.0
experiment.number_of_frames1200
experiment.wavelength0.082
experiment.sample_detector_distance3.561
experiment.concentration_minnull
experiment.concentration_max3.0
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experiment.flow_rate0.75
experiment.s_min0.06
experiment.s_max10.0
experiment.total_exposure_timenull
experiment.seccolumn1
fits[]
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versionnull
i0_calibration_standardnull
descriptionnull
experiment_descriptionSynchrotron SAXS data from solutions of ST9 RNA, PKmutant (59 nucleotides) in 50 mM Tris pH 7.5, 100 mM NaCl, 1 mM DTT, 10 mM MgCl2, 0.0002% w/v NaN3 were collected on the 16-ID (LiX) beam line at the National Synchrotron Light Source II (NSLS-II; Upton, NY, USA) using a Pilatus3 S 1M detector at a sample-detector distance of 3.6 m and at a wavelength of λ = 0.082 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 95.00 μl sample at 3 mg/ml was injected at a 0.75 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 20°C. 1200 successive 2 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.
tags[]
intensity_unitarbitrary
experimental_mw43.7
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mwnull
porod_mw_errornull
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pddf_i0_errornull
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guinier_i0_errornull
pddf_rg3.648
pddf_rg_errornull
guinier_rg3.52
guinier_rg_error0.024
pddf_dmax12.81
pddf_dmax_errornull
porod_volume61.9
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first8
guinier_point_last31
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDVZ4_datloglog_img.png
symmetrynull
last_modified2025-09-01T15:31:28.121164+02:00
bragg_peak[]
manifest.json:34 field values
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codeSASDVZ4
statussuccess
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View the complete summary.json source
{
  "code": "SASDVZ4",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/nm",
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    "title": "A conserved viral RNA fold enables nuclease resistance across kingdoms of life.",
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      "author_list": "Gezelle JG, Korn SM, McDonald JT, Gong Z, Erickson A, Huang CH, Yang F, Cronin M, Kuo YW, Wimberly BT, Steckelberg AL",
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View the complete manifest.json source
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