Bromodomain of EP300 liganded with BMS-536924. Determined by X-ray diffraction at 2.0 Å resolution. Released 12 Apr 2023.
Explore 7UGI in 3D Show helices and sheets RCSB PDB PDBe
7UGI contains 13 α-helices and 0 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 1051-1066 | 16 | |
| α-helix | 1073-1075 | 3 | |
| α-helix | 1081-1084 | 4 | |
| α-helix | 1089-1092 | 4 | |
| α-helix | 1099-1107 | 9 | |
| α-helix | 1114-1131 | 18 | |
| α-helix | 1137-1160 | 24 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 1051-1066 | 16 | |
| α-helix | 1073-1075 | 3 | |
| α-helix | 1089-1092 | 4 | |
| α-helix | 1099-1108 | 10 | |
| α-helix | 1114-1131 | 18 | |
| α-helix | 1137-1160 | 24 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone acetyltransferase p300 | A, B | protein | 116 | Homo sapiens | Q09472 (AlphaFold model) |
>7UGI_1 Histone acetyltransferase p300 (chains A, B) SMIFKPEELRQALMPTLEALYRQDPESLPFRQPVDPQLLGIPDYFDIVKSPMDLSTIKRK LDTGQYQEPWQYVDDIWLMFNNAWLYNRKTSRVYKYCSKLSEVFEQEIDPVMQSLG
| ID | Name | Formula | Copies |
|---|---|---|---|
| PE5 | 3,6,9,12,15,18,21,24-octaoxahexacosan-1-ol | C18 H38 O9 | 1 |
| N6I | (3M)-4-{[(2S)-2-(3-chlorophenyl)-2-hydroxyethyl]amino}-3-[4-methyl-6-(morpholin… | C25 H26 Cl N5 O3 | 2 |
Water and common crystallization additives (EDO) are not listed.
Structural basis of CBP and EP300 interaction with kinase inhibitors. Schonbrunn, E., Bikowitz, M. To be published.
Other PDB entries of the same protein (UniProt Q09472 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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