Allovalent scavenging of activation domains in the transcription factor ANAC013 gears transcriptional regulation.

Delaforge E, Due AD, Theisen FF, Morffy N, O'Shea C, Blackledge M, Strader LC, Skriver K, Kragelund BB, Nucleic Acids Res 53(4) (2025) Europe PMC

SASDU37 – The intrinsically disordered region of NAC domain-containing protein 13 (ANAC013; amino acids 161-274)

NAC domain-containing protein 13
MWexperimental 14 kDa
MWexpected 13 kDa
VPorod 36 nm3
log I(s) 1.01×10-2 1.01×10-3 1.01×10-4 1.01×10-5
NAC domain-containing protein 13 small angle scattering data  s, nm-1
ln I(s)
NAC domain-containing protein 13 Guinier plot ln 1.02×10-2 Rg: 3.6 nm 0 (3.6 nm)-2 s2
(sRg)2I(s)/I(0)
NAC domain-containing protein 13 Kratky plot 1.104 0 3 sRg
p(r)
NAC domain-containing protein 13 pair distance distribution function Rg: 3.7 nm 0 Dmax: 16 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of ANAC013 (amino acids 161-274) in 20 mM HEPES, 150 mM NaCl, 5 mM NaNO3, 5 mM TCEP, pH 7.4 were collected on the EMBL P12 beam line at PETRA III (DESY; Hamburg, Germany) using a Pilatus 6M detector at a sample-detector distance of 3 m and at a wavelength of λ = 0.123981 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 70.00 μl sample at 9.1 mg/ml was injected at a 0.65 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 20°C. 2220 successive 1 second frames were collected through the entire SEC elution; 36 sample frames were used for averaging. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.

Tags: idp
NAC domain-containing protein 13 (ANAC013 (IDR))
Mol. type   Protein
Organism   Arabidopsis thaliana
Olig. state   Monomer
Mon. MW   12.6 kDa
 
UniProt   F4IED2 (161-274)
Sequence   FASTA