PDB-7jjg: Crystal structure of the second bromodomain (BD2) of human TAF1 bound to ATR kinase inhibitor AZ20 Method: X-RAY DIFFRACTION / Resolution: 1.6 Å
PDB-7jjh: Crystal structure of the unliganded tandem bromodomain (BD1, BD2) of human TAF1 Method: X-RAY DIFFRACTION / Resolution: 2.1 Å
PDB-7jsp: Crystal structure of the second bromodomain (BD2) of human TAF1 bound to ATR kinase inhibitor AZD6738 Method: X-RAY DIFFRACTION / Resolution: 1.7 Å
PDB-7k03: Crystal structure of the tandem bromodomain (BD1 and BD2) of human TAF1 bound to ATR kinase inhibitor AZD6738 Method: X-RAY DIFFRACTION / Resolution: 1.6 Å
PDB-7k0d: Crystal structure of the tandem bromodomain (BD1, BD2) of human TAF1 bound to mTORC1/2 inhibitor AZD3147 Method: X-RAY DIFFRACTION / Resolution: 2.2 Å
PDB-7k0u: Crystal structure of the second bromodomain (BD2) of human TAF1 bound to PLK1 kinase inhibitor BI2536 Method: X-RAY DIFFRACTION / Resolution: 2.52 Å
PDB-7k1p: Crystal structure of the second bromodomain (BD2) of human TAF1 bound to bromosporine Method: X-RAY DIFFRACTION / Resolution: 2.45 Å
PDB-7k27: Crystal structure of the tandem bromodomain (BD1, BD2) of human TAF1 bound to ATR inhibitor AZ20 Method: X-RAY DIFFRACTION / Resolution: 1.5 Å
PDB-7k3o: Crystal structure of the unliganded second bromodomain (BD2) of human TAF1 Method: X-RAY DIFFRACTION / Resolution: 1.7 Å
PDB-7k42: Crystal structure of the second bromodomain (BD2) of human TAF1 bound to dioxane Method: X-RAY DIFFRACTION / Resolution: 1.7 Å
PDB-7k6f: Crystal structure of the tandem bromodomain (BD1, BD2) of human TAF1 in complex with MES (2-(N-morpholino)ethanesulfonic acid) Method: X-RAY DIFFRACTION / Resolution: 1.86 Å
PDB-7l6x: Crystal structure of the tandem bromodomain (BD1, BD2) of human TAF1 bound to GNE-371 Method: X-RAY DIFFRACTION / Resolution: 2.75 Å
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