5BT3: EP300 bromodomain

Crystal structure of EP300 bromodomain in complex with SGC-CBP30 chemical probe. Determined by X-ray diffraction at 1.05 Å resolution. Released 1 Jul 2015.

Method
X-ray diffraction
Resolution
1.05 Å
Organism
Homo sapiens
Chains
1
Atoms
1,205
Mol. weight
14.4 kDa
Ligands
2LO, IPA
Released
1 Jul 2015

Explore 5BT3 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5BT3 contains 7 α-helices and 0 β-strands across 1 chain. 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.

Chain A: 7 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix1051-106616
α-helix1073-10753
α-helix1081-10844
α-helix1089-10924
α-helix1099-11079
α-helix1114-113118
α-helix1137-116024

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone acetyltransferase p300Aprotein116Homo sapiensQ09472 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5BT3_1 Histone acetyltransferase p300 (chains A)
SMIFKPEELRQALMPTLEALYRQDPESLPFRQPVDPQLLGIPDYFDIVKSPMDLSTIKRK
LDTGQYQEPWQYVDDIWLMFNNAWLYNRKTSRVYKYCSKLSEVFEQEIDPVMQSLG

Ligands and cofactors

IDNameFormulaCopies
2LO2-[2-(3-chloro-4-methoxyphenyl)ethyl]-5-(3,5-dimethyl-1,2-oxazol-4-yl)-1-[(2S)-…C28 H33 Cl N4 O31
IPAIsopropyl alcoholC3 H8 O1

Primary citation

Crystal structure of EP300 bromodomain in complex with a 3,5-dimethylisoxazol ligand. Tallant, C., Hay, D., Krojer, T. et al. To be published.

Other PDB entries of the same protein (UniProt Q09472 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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