The conserved yeast protein Knr4 involved in cell wall integrity is a multi-domain intrinsically disordered protein.

Batista M, Donker EIM, Bon C, Guillien M, Caisso A, Mourey Funding L, Marie François Funding J, Maveyraud L, Zerbib D, J Mol Biol :168048 (2023) Europe PMC

SASDPD7 – C-terminal truncated KNR4

Cell wall assembly regulator SMI1
MWI(0) 38 kDa
MWexpected 40 kDa
VPorod 79 nm3
log I(s) 2.29×101 2.29×100 2.29×10-1 2.29×10-2
Cell wall assembly regulator SMI1 small angle scattering data  s, nm-1
ln I(s)
Cell wall assembly regulator SMI1 Guinier plot ln 2.30×101 Rg: 2.8 nm 0 (2.8 nm)-2 s2
(sRg)2I(s)/I(0)
Cell wall assembly regulator SMI1 Kratky plot 1.104 0 3 sRg
p(r)
Cell wall assembly regulator SMI1 pair distance distribution function Rg: 3.1 nm 0 Dmax: 11 nm

Data validation


Fits and models


log I(s)
 s, nm-1
Cell wall assembly regulator SMI1 DAMMIN model

Synchrotron SAXS data from solutions of C-terminal truncated KNR4 in 100 mM MES, 300 mM NaCl, pH 6 were collected on the BM29 beam line at the ESRF (Grenoble, France) using a Pilatus 1M detector at a sample-detector distance of 2.9 m and at a wavelength of λ = 0.09919 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 9 mg/ml was injected at a 0.50 ml/min flow rate onto a column at 20°C. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.

X-ray Exposure time = UNKNOWN. Number of frames = UNKNOWN. SEC column = UNKNOWN

Cell wall assembly regulator SMI1 (KNR4-ΔC)
Mol. type   Protein
Organism   Saccharomyces cerevisiae (strain ATCC 204508 / S288c)
Olig. state   Monomer
Mon. MW   39.6 kDa
 
UniProt   P32566 (1-345)
Sequence   FASTA