9NN4: BET BRD3-BD1

BET BRD3-BD1 in complex with peptide 7.2. Determined by X-ray diffraction at 1.37 Å resolution. Released 11 Feb 2026.

Method
X-ray diffraction
Resolution
1.37 Å
Organisms
Homo sapiens, synthetic construct
Chains
4
Atoms
2,533
Mol. weight
31.2 kDa
Released
11 Feb 2026

Explore 9NN4 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 8 helices, 2 β-strands

ElementResiduesLengthSheet
β-strand3611
α-helix37-415
α-helix42-476
α-helix48-514
α-helix54-596
α-helix73-764
α-helix83-919
α-helix98-11518
α-helix121-13818
β-strand14611
Chain B: 9 helices, 2 β-strands
ElementResiduesLengthSheet
β-strand3612
α-helix37-415
α-helix42-476
α-helix48-514
α-helix54-596
α-helix65-684
α-helix73-764
α-helix83-919
α-helix98-11518
α-helix121-13919
β-strand14612
Chain D: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix89-913
Chain E: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix7-93

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Bromodomain-containing protein 3A, Bprotein120Homo sapiensQ15059 (AlphaFold model)
peptide 7.2D, Eprotein11synthetic construct
Sequence of entity 1 (A, B), FASTA
>9NN4_1 Bromodomain-containing protein 3 (chains A, B)
NPSKPGRKTNQLQYMQNVVVKTLWKHQFAWPFYQPVDAIKLNLPDYHKIIKNPMDMGTIK
KRLENNYYWSASECMQDFNTMFTNCYIYNKPTDDIVLMAQALEKIFLQKVAQMPQEEVEL
Sequence of entity 2 (D, E), FASTA
>9NN4_2 peptide 7.2 (chains D, E)
XYQRKPRKLCX

Primary citation

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:

Browse structure collections

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