Allosteric network of dynamic coupling within BAP1-UCH revealed by methyl NMR

Yong-Sheng Wang.

SASDXE6 – Ubiquitin C-terminal hydrolase (UCH) domain of BAP1 point mutation (L49V)

Ubiquitin C-terminal hydrolase (UCH) domain of BAP1 L49V
MWexperimental 27 kDa
MWexpected 27 kDa
VPorod 36 nm3
log I(s) 1.17×10-1 1.17×10-2 1.17×10-3 1.17×10-4
Ubiquitin C-terminal hydrolase (UCH) domain of BAP1 L49V small angle scattering data  s, nm-1
ln I(s)
Ubiquitin C-terminal hydrolase (UCH) domain of BAP1 L49V Guinier plot ln 1.17×10-1 Rg: 2.2 nm 0 (2.2 nm)-2 s2
(sRg)2I(s)/I(0)
Ubiquitin C-terminal hydrolase (UCH) domain of BAP1 L49V Kratky plot 1.104 0 3 sRg
p(r)
Ubiquitin C-terminal hydrolase (UCH) domain of BAP1 L49V pair distance distribution function Rg: 2.2 nm 0 Dmax: 8.7 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of Ubiquitin C-terminal hydrolase (UCH) domain of BAP1 point mutation (L49V) in 20 mM HEPES, 150 mM NaCl, 1 mM TCEP, 0.02% NaN3, pH 7.5 were collected on the 13A beam line at the Taiwan Photon Source, NSRRC storage ring (Hsinchu, Taiwan) using a Eiger X 1M and Eiger X 9M detector at a sample-detector distance of 9 m and at a wavelength of λ = 0.0826 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 90.00 μl sample at 12 mg/ml was injected at a 0.10 ml/min flow rate onto a Agilent Bio SEC-3, 300 Å column at 10°C. 11 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.

Ubiquitin C-terminal hydrolase (UCH) domain of BAP1 L49V
Mol. type   Protein
Olig. state   Monomer
Mon. MW   27.2 kDa
 
UniProt   Q92560 (1-238)
Sequence   FASTA