Henipavirus W proteins

Frank Gondelaud.

SASDQR9 – Hendra W protein C123-only mutant

Protein W mutant (C316S, C334S, C419S)
MWexperimental 90 kDa
MWexpected 105 kDa
log I(s) 6.51×10-2 6.51×10-3 6.51×10-4 6.51×10-5
Protein W mutant (C316S, C334S, C419S) small angle scattering data  s, nm-1
ln I(s)
Protein W mutant (C316S, C334S, C419S) Guinier plot ln 6.52×10-2 Rg: 8.1 nm 0 (8.1 nm)-2 s2
(sRg)2I(s)/I(0)
Protein W mutant (C316S, C334S, C419S) Kratky plot 1.104 0 3 sRg
Dmax: 37 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of Hendra W protein (C123-only mutant) in 20 mM HEPES, 150 mM NaCl, pH 7.2 were collected on the SWING beam line at SOLEIL (Saint-Aubin, France) using a Eiger 4M detector at a sample-detector distance of 2 m and at a wavelength of λ = 0.103 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 4.7 mg/ml was injected at a 0.30 ml/min flow rate onto a Agilent Bio SEC-3, 300 Å column at 20°C. 810 successive 0.990 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.

Protein W mutant (C316S, C334S, C419S) (WHeV)
Mol. type   Protein
Organism   Hendra virus (isolate Horse/Autralia/Hendra/1994)
Olig. state   Dimer
Mon. MW   52.5 kDa
 
UniProt   P0C1C6 (2-447)
Sequence   FASTA