Discovery of Dual TAF1-ATR Inhibitors and Ligand-Induced Structural Changes of the TAF1 Tandem Bromodomain.

Karim RM, Yang L, Chen L, Bikowitz MJ, Lu J, Grassie D, Shultz ZP, Lopchuk JM, Chen J, Schönbrunn E, J Med Chem 65(5):4182-4200 (2022) Europe PMC

SASDK72 – TAF1 tandem bromodomain with inhibitor BAY299

Transcription initiation factor II D
MWexperimental 65 kDa
MWexpected 31 kDa
VPorod 106 nm3
log I(s) 3.81×100 3.81×10-1 3.81×10-2 3.81×10-3
Transcription initiation factor II D small angle scattering data  s, nm-1
ln I(s)
Transcription initiation factor II D Guinier plot ln 3.81×100 Rg: 3.6 nm 0 (3.6 nm)-2 s2
(sRg)2I(s)/I(0)
Transcription initiation factor II D Kratky plot 1.104 0 3 sRg
p(r)
Transcription initiation factor II D pair distance distribution function Rg: 3.7 nm 0 Dmax: 12.5 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of TAF1 tandem bromodomain with inhibitor BAY299 in 50 mM HEPES, 5% v/v ethylene glycol, 2.5% v/v DMSO and 2 mM DTT, pH 7.5 were collected on the BioCAT 18ID beam line at the Advanced Photon Source (APS), Argonne National Laboratory storage ring (Lemont, IL, USA) using a Pilatus3 X 1M detector at a sample-detector distance of 3.5 m and at a wavelength of λ = 0.10332 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). One solute concentration of 1.50 mg/ml was measured at 25°C. 1900 successive 0.500 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.

Experiments were conducted at room temperature in 50 mM HEPES (pH7.5), 5% v/v ethylene glycol, 2.5% v/v DMSO and 2 mM DTT. Ab initio shape models of TAF1-T were generated using DENSS for electron density map generation and bead modeling by DAMMIN. Multiple runs were performed to generate 20 starting models, and the final ab initio shape was reconstructed by averaging and refining the starting models. The low-resolution electron density maps generated by DENSS and the bead models computed by DAMFILT of the ATSAS suit are shown in the associated publication. Isolated models of BD1 and BD2 omitting flexible regions of the N- and C-termini (1371 -1376 and 1631 – 1635) served for rigid body fitting into the electron density maps using PHENIX (dock_in_map) and Chimera. The hinge region connecting the two domains was modeled using ModLoop49. Iterative refinement cycles were applied using Crysol 3.0 to achieve models that satisfied the experimental data.

Transcription initiation factor II D (TAF1)
Mol. type   Protein
Organism   Escherichia coli
Olig. state   Monomer
Mon. MW   30.9 kDa
 
UniProt   P21675 (1373-1635)
Sequence   FASTA