Human FASTK protein

Daria Dawidziak.

SASDVV2 – Fas-activated serine/threonine kinase/phosphoprotein FASTK (76-549)

Fas-activated serine/threonine kinase (amino acids 76-549)
MWI(0) 64 kDa
MWexpected 53 kDa
VPorod 96 nm3
log I(s) 3.29×10-2 3.29×10-3 3.29×10-4 3.29×10-5
Fas-activated serine/threonine kinase (amino acids 76-549) small angle scattering data  s, nm-1
ln I(s)
Fas-activated serine/threonine kinase (amino acids 76-549) Guinier plot ln 3.29×10-2 Rg: 3.6 nm 0 (3.6 nm)-2 s2
(sRg)2I(s)/I(0)
Fas-activated serine/threonine kinase (amino acids 76-549) Kratky plot 1.104 0 3 sRg
p(r)
Fas-activated serine/threonine kinase (amino acids 76-549) pair distance distribution function Rg: 3.8 nm 0 Dmax: 16.3 nm

Data validation


Fits and models


log I(s)
 s, nm-1

Synchrotron SAXS data from solutions of Fas-activated serine/threonine kinase/phosphoprotein FASTK (76-549) in 50 mM Tris-HCl, 5% (v/v) Glycerol, 200 mM Ammonium Sulphate, 50 mM NaCl, 0.5 mM TCEP, 10 mM Glutamic acid, 10 mM Arginine;, pH 8.5 were collected on the B21 beam line at the Diamond Light Source storage ring (Didcot, UK) using a Eiger 4M detector at a sample-detector distance of 3.7 m and at a wavelength of λ = 0.094 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 45.00 μl sample at 8.9 mg/ml was injected at a 0.08 ml/min flow rate onto a GE Superdex 200 Increase 3.2/300 column at 15°C. 620 successive 3 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.

To obtain P(r) data were processed with BIFT based on q range (1/A) 0.0046 to 0.1604

Fas-activated serine/threonine kinase (amino acids 76-549) (FASTK)
Mol. type   Protein
Organism   Homo sapiens
Olig. state   Monomer
Mon. MW   53.3 kDa
 
UniProt   Q14296 (76-549)
Sequence   FASTA