SARS-CoV-2 N-protein variants: IDL176-246

Guillem Hernandez.

SASDVT6 – SARS-CoV-2 N-protein InterDomain Linker (IDL, amino acids 176-245) L223P, L227P and L230P triple mutant: 1667 µM

Nucleoprotein (L223P, L227P, L230P)
MWI(0) 12 kDa
MWexpected 8 kDa
VPorod 14 nm3
log I(s) 6.95×101 6.95×100 6.95×10-1 6.95×10-2
Nucleoprotein (L223P, L227P, L230P) small angle scattering data  s, nm-1
ln I(s)
Nucleoprotein (L223P, L227P, L230P) Guinier plot ln 6.95×101 Rg: 2.8 nm 0 (2.8 nm)-2 s2
(sRg)2I(s)/I(0)
Nucleoprotein (L223P, L227P, L230P) Kratky plot 1.104 0 3 sRg
p(r)
Nucleoprotein (L223P, L227P, L230P) pair distance distribution function Rg: 2.9 nm 0 Dmax: 12 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of the SARS-CoV-2 N-protein inter-domain linker triple mutant (IDL, amino acids 176-245; L223P, L227P and L230P) in 100 mM Tris-HCl, 150 mM NaCl, 1 mM EDTA, pH 8 were collected on the BM29 beam line at the ESRF (Grenoble, France) using a Pilatus 1M detector at a sample-detector distance of 2.8 m and at a wavelength of λ = 0.0999 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 14.00 mg/ml was measured at 10°C. 10 successive 2 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.

Nucleoprotein (L223P, L227P, L230P) (N-protein LP mutant)
Mol. type   Protein
Organism   Severe acute respiratory syndrome coronavirus 2
Olig. state   Monomer
Mon. MW   8.3 kDa
 
UniProt   P0DTC9 (176-245)
Sequence   FASTA