2. Measurements Reported by SASBDB Reported Results
Metric
Method
Value
Uncertainty
Unit
dmax
P(r)
12.84
—
Å
i0
Guinier
0.13
0.00011
arbitrary
i0
P(r)
0.1299
—
arbitrary
mw
Experimental
100.0
—
kDa
mw
Porod
89.2
—
kDa
porod_volume
Porod
151.6
—
ų
rg
Guinier
3.68
0.013
Å
rg
P(r)
3.74
—
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/q6/sasddq6/source/SASDDQ6.dat
downloaded
32262
full_entry_zip
sasbdb/entries/q6/sasddq6/source/SASDDQ6.zip
downloaded
23083
pddf
sasbdb/entries/q6/sasddq6/source/SASDDQ6.out
downloaded
52406
sascif
sasbdb/entries/q6/sasddq6/source/SASDDQ6.sascif
downloaded
75687
summary
sasbdb/entries/q6/sasddq6/source/summary.json
downloaded
8268
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5. Experiment Description and Publication Experiment & Publication
Original Experiment Description
Synchrotron SAXS data, I(s) vs s (s = 4π sin θ/λ, where 2θ is the scattering angle) were collected from a sample of ferredoxin protease, FusC, using continuous-flow size-exclusion chromatography SAXS (SEC-SAXS) at the SAXS/WAXS beam line at the Australian Synchrotron (Melbourne, Australia). Data were collected a using a Pilatus 1M detector at a sample-detector distance of 2.7 m and at a wavelength of λ = 0.103 nm. The SEC mobile phase consisted of 20 mM Tris, 150 mM NaCl, 0.03 % NaN3, 5.0 % v/v glycerol, pH 7.8, (20°C). The SAXS data data measured from the SEC-elution (sample peak and buffer) were normalized to the intensity of the transmitted beam and radially averaged. The data from the sample SEC-peak were scaled and averaged and the scattering of the solvent-blank was subtracted from the sample frames to produce the data displayed in this entry.
Related Publication
Title
FusC, a member of the M16 protease family acquired by bacteria for iron piracy against plants.
Authors
Grinter R, Hay ID, Song J, Wang J, Teng D, Dhanesakaran V, Wilksch JJ, Davies MR, Littler D, Beckham SA, Henderson IR, Strugnell RA, Dougan G, Lithgow T
DOI / PMID
10.1371/journal.pbio.2006026 / 30071011
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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.
Every source field is expanded here, including empty values, list members and fields already shown above.
summary.json:134 field values
Field path
Raw value
code
SASDDQ6
status
Published
type_of_curve
SEC-SAS
angular_unit
1/A
project.title
FusC, a member of the M16 protease family acquired by bacteria for iron piracy against plants.
project.publication.title
FusC, a member of the M16 protease family acquired by bacteria for iron piracy against plants.
project.publication.author_list
Grinter R, Hay ID, Song J, Wang J, Teng D, Dhanesakaran V, Wilksch JJ, Davies MR, Littler D, Beckham SA, Henderson IR, Strugnell RA, Dougan G, Lithgow T
Synchrotron SAXS data, I(s) vs s (s = 4π sin θ/λ, where 2θ is the scattering angle) were collected from a sample of ferredoxin protease, FusC, using continuous-flow size-exclusion chromatography SAXS (SEC-SAXS) at the SAXS/WAXS beam line at the Australian Synchrotron (Melbourne, Australia). Data were collected a using a Pilatus 1M detector at a sample-detector distance of 2.7 m and at a wavelength of λ = 0.103 nm. The SEC mobile phase consisted of 20 mM Tris, 150 mM NaCl, 0.03 % NaN3, 5.0 % v/v glycerol, pH 7.8, (20°C). The SAXS data data measured from the SEC-elution (sample peak and buffer) were normalized to the intensity of the transmitted beam and radially averaged. The data from the sample SEC-peak were scaled and averaged and the scattering of the solvent-blank was subtracted from the sample frames to produce the data displayed in this entry.