2. Measurements Reported by SASBDB Reported Results
Metric
Method
Value
Uncertainty
Unit
dmax
P(r)
11.91
—
Å
i0
Guinier
0.393384
—
1/cm
i0
P(r)
0.3786
—
1/cm
mw
Experimental
334.0
—
kDa
mw
Guinier I(0)
334.0
11.0
kDa
rg
Guinier
4.37
0.07
Å
rg
P(r)
4.08
—
Å
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.
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4. Source File Index Source Files
Category
Path
Download status
Size
curve
sasbdb/entries/f3/sasdwf3/source/SASDWF3.dat
downloaded
4786
full_entry_zip
sasbdb/entries/f3/sasdwf3/source/SASDWF3.zip
downloaded
5601
pddf
sasbdb/entries/f3/sasdwf3/source/SASDWF3.out
downloaded
10360
sascif
sasbdb/entries/f3/sasdwf3/source/SASDWF3.sascif
not_available
—
summary
sasbdb/entries/f3/sasdwf3/source/summary.json
downloaded
7611
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5. Experiment Description and Publication Experiment & Publication
Original Experiment Description
SANS data from solutions of the Circadian clock protein KaiC (hydrogenated-KaiC) in 50 mM sodium phosphate buffer, 150 mM NaCl, 5 mM MgCl₂, 0.5 mM EDTA, 1 mM ATP, 1 mM DTT, 50 mM arginine, 50 mM glutamine, 100% v/v D₂O, pH 7.8 were collected on the SANS-U beam line at JRR-3 (Japan Atomic Energy Agency; Ibaraki, Japan) using a ORDELA, model 2660N detector at a sample-detector distance of 4 and 1.03 m at a wavelength of λ = 0.6 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Stop-flow mode In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 0.50 μl sample at 5.6 mg/ml was injected onto a Cytiva Superdex 200 Increase 10/300 column at 25°C. 24 successive 600 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.
Related Publication
Title
Size-exclusion chromatography–small-angle neutron scattering system optimized for an instrument with medium neutron flux
Authors
Morishima K, Inoue R, Nakagawa T, Shimizu M, Sakamoto R, Oda T, Mayumi K, Sugiyama M
DOI / PMID
10.1107/S1600576725000779 / —
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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.
SANS data from solutions of the Circadian clock protein KaiC (hydrogenated-KaiC) in 50 mM sodium phosphate buffer, 150 mM NaCl, 5 mM MgCl₂, 0.5 mM EDTA, 1 mM ATP, 1 mM DTT, 50 mM arginine, 50 mM glutamine, 100% v/v D₂O, pH 7.8 were collected on the SANS-U beam line at JRR-3 (Japan Atomic Energy Agency; Ibaraki, Japan) using a ORDELA, model 2660N detector at a sample-detector distance of 4 and 1.03 m at a wavelength of λ = 0.6 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). Stop-flow mode In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 0.50 μl sample at 5.6 mg/ml was injected onto a Cytiva Superdex 200 Increase 10/300 column at 25°C. 24 successive 600 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.