A homologue of the Parkinson's disease-associated protein LRRK2 undergoes a monomer-dimer transition during GTP turnover.

Deyaert E, Wauters L, Guaitoli G, Konijnenberg A, Leemans M, Terheyden S, Petrovic A, Gallardo R, Nederveen-Schippers LM, Athanasopoulos PS, Pots H, Van Haastert PJM, Sobott F, Gloeckner CJ, Efremov R, Kortholt A, Versées W, Nat Commun 8(1):1008 (2017) Europe PMC

SASDCE2 – Rab family protein CtRoco L487A GDP

Rab family protein
MWexperimental 257 kDa
MWexpected 254 kDa
VPorod 469 nm3
log I(s) 1.35×10-1 1.35×10-2 1.35×10-3 1.35×10-4
Rab family protein small angle scattering data  s, nm-1
ln I(s)
Rab family protein Guinier plot ln 1.36×10-1 Rg: 5.9 nm 0 (5.9 nm)-2 s2
(sRg)2I(s)/I(0)
Rab family protein Kratky plot 1.104 0 √3 sRg
p(r)
Rab family protein pair distance distribution function Rg: 6.0 nm 0 Dmax: 21.8 nm

Data validation

There are no models related to this curve.

Synchrotron SAXS data from solutions of Rab family protein CtRoco L487A GDP in 20 mM HEPES 150 mM NaCl 5 mM MgCl2 5% Glycerol 1 mM DTT 200µM GDP, pH 7.5 were collected on the SWING camera on the storage ring SOLEIL (Saint-Aubin, France) using a CCD AVIEX detector at a wavelength of λ = 0.103 nm (I(s) vs s, where s = 4πsin θ/λ and 2θ is the scattering angle). Inline SEC-SAXS was employed at 25°C (50 µl injection volume of an 8 mg/ml protein solution on a Bio SEC-3 HPLC column (Agilent, 3 µm 300 Å)). 36 successive 0.750 second frames were collected through the elution peak. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted and the different curves were scaled and averaged to produce the final SAXS data displayed in this entry.

Storage temperature = UNKNOWN. Sample detector distance = UNKNOWN

Rab family protein (CtRoco)
Mol. type   Protein
Organism   Chlorobaculum tepidum
Olig. state   Dimer
Mon. MW   127.1 kDa
 
UniProt   Q8KC98 (1-1102)
Sequence   FASTA