BET BRD3-BD1 in complex with peptide 7.2. Determined by X-ray diffraction at 1.37 Å resolution. Released 11 Feb 2026.
Explore 9NN4 in 3D Show helices and sheets RCSB PDB PDBe
9NN4 contains 19 α-helices and 4 β-strands across 4 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 |
|---|---|---|---|
| β-strand | 36 | 1 | 1 |
| α-helix | 37-41 | 5 | |
| α-helix | 42-47 | 6 | |
| α-helix | 48-51 | 4 | |
| α-helix | 54-59 | 6 | |
| α-helix | 73-76 | 4 | |
| α-helix | 83-91 | 9 | |
| α-helix | 98-115 | 18 | |
| α-helix | 121-138 | 18 | |
| β-strand | 146 | 1 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 36 | 1 | 2 |
| α-helix | 37-41 | 5 | |
| α-helix | 42-47 | 6 | |
| α-helix | 48-51 | 4 | |
| α-helix | 54-59 | 6 | |
| α-helix | 65-68 | 4 | |
| α-helix | 73-76 | 4 | |
| α-helix | 83-91 | 9 | |
| α-helix | 98-115 | 18 | |
| α-helix | 121-139 | 19 | |
| β-strand | 146 | 1 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 89-91 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 7-9 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Bromodomain-containing protein 3 | A, B | protein | 120 | Homo sapiens | Q15059 (AlphaFold model) |
| peptide 7.2 | D, E | protein | 11 | synthetic construct |
>9NN4_1 Bromodomain-containing protein 3 (chains A, B) NPSKPGRKTNQLQYMQNVVVKTLWKHQFAWPFYQPVDAIKLNLPDYHKIIKNPMDMGTIK KRLENNYYWSASECMQDFNTMFTNCYIYNKPTDDIVLMAQALEKIFLQKVAQMPQEEVEL
>9NN4_2 peptide 7.2 (chains D, E) XYQRKPRKLCX
The effect of peptide size on target affinity in mRNA display-derived macrocyclic peptides. Jing, X., Suh, J., Maxwell, J. et al. Chem Commun (Camb) (2026) 62:4028-4031. DOI 10.1039/d5cc06167a · PubMed
Other PDB entries of the same protein (UniProt Q15059 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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