Synchrotron SAXS
data from solutions of
Light state solution structure of Aureochrome1a- A´α-LOV-Jα
in
10 mM Tris 300 mM NaCl, pH 8
were collected
on the
BM29 beam line
at the ESRF storage ring
(Grenoble, France)
using a Pilatus 1M detector
at a sample-detector distance of 2.4 m and
at a wavelength of λ = 0.93 nm
(I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle).
Solute concentrations ranging between 0.8 and 15 mg/ml were measured
.
10 successive
20 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.
The low angle data collected at lower concentration were merged with the highest concentration high angle data to yield the final composite scattering curve.
Solution scattering data of Aureochrome1a- A´α-LOV-Jα in the light state (blue light illuminated for 5-10 min). The measurement was performed at two concentration 42 and 833 micomolar concentration. The buffer-only scattering was subtracted and the data sets were merged to generate representative curve. The analysis was performed using the ATSAS package. The displayed model is an averaged and volume corrected dummy atom representation (DAMFILT). For further sequence information refer to the Joint Genome Institute (JGI) entry JGI-49116.
|
Aureochrome1a-A´α-LOV-Jα
(Aureochrome1a-A)
|
Mol. type |
|
Protein |
Organism |
|
Phaeodactylum tricornutum |
Olig. state |
|
Dimer |
Mon. MW |
|
18.0 kDa |
Sequence |
|
FASTA |
|
|