Molecular basis of the regulation of full-length Nedd4-2 through calcium and 14-3-3 proteins

Veronika Obšilová.

SASDUB3 – 14-3-3 eta human

14-3-3 protein eta
MWexperimental 56 kDa
MWexpected 57 kDa
VPorod 85 nm3
log I(s) 8.42×10-2 8.42×10-3 8.42×10-4 8.42×10-5
14-3-3 protein eta small angle scattering data  s, nm-1
ln I(s)
14-3-3 protein eta Guinier plot ln 8.43×10-2 Rg: 2.9 nm 0 (2.9 nm)-2 s2
(sRg)2I(s)/I(0)
14-3-3 protein eta Kratky plot 1.104 0 3 sRg
p(r)
14-3-3 protein eta pair distance distribution function Rg: 2.9 nm 0 Dmax: 8.4 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of 14-3-3 protein eta in 20 mM HEPES, 150 mM NaCl, 1 mM TCEP, 1 mM EDTA, 3% glycerol, pH 7.5 were collected on the EMBL P12 beam line at PETRA III (DESY; Hamburg, Germany) using a Pilatus 6M detector at a sample-detector distance of 3 m and at a wavelength of λ = 0.123982 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 50.00 μl sample at 7.6 mg/ml was injected at a 0.30 ml/min flow rate onto a GE Superdex 200 Increase 5/150 column at 20°C. 1800 successive 0.495 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.

14-3-3 protein eta (14-3-3 eta human)
Mol. type   Protein
Organism   Homo sapiens
Olig. state   Dimer
Mon. MW   28.4 kDa
 
UniProt   Q04917 (1-246)
Sequence   FASTA