Full-length G3BP1 (residues 1-466) at pH 6.0, 150 mM NaCl

SASDYT6 – Full-length Ras GTPase-activating protein-binding protein 1, G3BP1 (residues 1-466) at pH 6.0, 150 mM NaCl

Ras GTPase-activating protein-binding protein 1
MWexperimental 113 kDa
MWexpected 105 kDa
VPorod 159 nm3
log I(s) 5.47×103 5.47×102 5.47×101 5.47×100
Ras GTPase-activating protein-binding protein 1 small angle scattering data  s, nm-1
ln I(s)
Ras GTPase-activating protein-binding protein 1 Guinier plot ln 5.47×103 Rg: 5 nm 0 (5 nm)-2 s2
(sRg)2I(s)/I(0)
Ras GTPase-activating protein-binding protein 1 Kratky plot 1.104 0 3 sRg
p(r)
Ras GTPase-activating protein-binding protein 1 pair distance distribution function Rg: 5.3 nm 0 Dmax: 22.5 nm

Data validation


Fits and models


log I(s)
 s, nm-1
Ras GTPase-activating protein-binding protein 1 DAMMIN model

log I(s)
 s, nm-1
Ras GTPase-activating protein-binding protein 1 CORAL model

Synchrotron SAXS data from solutions of G3BP1 in 50mM MES pH 6, 150mM NaCl, 1mM DTT, 1% glycerol, 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 = 0.124 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 60.00 μl sample at 8.5 mg/ml was injected at a 0.75 ml/min flow rate onto a GE Superdex 200 Increase 5/150 column at 25°C. 22 successive 1 second frames were collected through the SEC elution peak of the sample. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.

Ras GTPase-activating protein-binding protein 1 (G3BP1)
Mol. type   Protein
Organism   Homo sapiens
Olig. state   Dimer
Mon. MW   52.5 kDa
 
UniProt   Q13283 (1-466)
Sequence   FASTA