2. Measurements Reported by SASBDB Reported Results
Metric
Method
Value
Uncertainty
Unit
dmax
P(r)
7.05
—
Å
i0
Guinier
0.0218267
—
1/cm
i0
P(r)
0.1696971
—
1/cm
mw
Experimental
33.434
—
kDa
mw
Porod
33.434
—
kDa
porod_volume
Porod
55.5
—
ų
rg
Guinier
2.144
0.012
Å
rg
P(r)
2.18
—
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/v7/sasduv7/source/SASDUV7.dat
downloaded
90657
full_entry_zip
sasbdb/entries/v7/sasduv7/source/SASDUV7.zip
downloaded
30930
pddf
sasbdb/entries/v7/sasduv7/source/SASDUV7.out
downloaded
3916
sascif
sasbdb/entries/v7/sasduv7/source/SASDUV7.sascif
not_available
—
summary
sasbdb/entries/v7/sasduv7/source/summary.json
downloaded
7834
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5. Experiment Description and Publication Experiment & Publication
Original Experiment Description
Synchrotron SAXS data from solutions of the tandem SH2 domains of Tyrosine-protein kinase SYK with a bound CD3G diphospho-ITAM peptide in 10 mM HEPES, 150 mM NaCl, 1 mM TCEP, pH 7.5 were collected on the B21 beam line at the Diamond Light Source (Didcot, UK) using a Eiger 4M detector at a sample-detector distance of 3.7 m and at a wavelength of λ = 0.09408 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 45.00 μl sample at 10 mg/ml was injected at a 0.08 ml/min flow rate onto a GE Superdex 75 Increase 5/150 column at 15°C. 600 successive 3 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
The mechanism of allosteric activation of SYK kinase derived from multiple phospho-ITAM-bound structures
Authors
Bradshaw W, Harris G, Gileadi O, Katis V
DOI / PMID
10.1016/j.str.2024.09.024 / —
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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.
Synchrotron SAXS data from solutions of the tandem SH2 domains of Tyrosine-protein kinase SYK with a bound CD3G diphospho-ITAM peptide in 10 mM HEPES, 150 mM NaCl, 1 mM TCEP, pH 7.5 were collected on the B21 beam line at the Diamond Light Source (Didcot, UK) using a Eiger 4M detector at a sample-detector distance of 3.7 m and at a wavelength of λ = 0.09408 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 45.00 μl sample at 10 mg/ml was injected at a 0.08 ml/min flow rate onto a GE Superdex 75 Increase 5/150 column at 15°C. 600 successive 3 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.