› 7l72

X-ray diffraction
1.5Å resolution

Crystal structure of the second bromodomain (BD2) of human BRD3 bound to Ro3280

Released:
DOI: 10.2210/pdb7l72/pdb
PDB entry 7l72 coloured by chain, front view.
PDB entry 7l72 coloured by chain, side view.
PDB entry 7l72 coloured by chain, top view.
Source organism: Homo sapiens
Primary publication:
Differential BET Bromodomain Inhibition by Dihydropteridinone and Pyrimidodiazepinone Kinase Inhibitors.
Karim RM, Bikowitz MJ, Chan A, Zhu JY, Grassie D, Becker A, Berndt N, Gunawan S, Lawrence NJ, Schönbrunn E
J Med Chem 64 15772-15786 (2021)
PMID: 34710325

Function and Biology Details

Biochemical function:
  • not assigned
Biological process:
  • not assigned
Cellular component:
  • not assigned
Sequence domains:

Structure analysis Details

Assembly composition:
monomeric (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-172178 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Bromodomain-containing protein 3 Chain: A
Molecule details ›
Chain: A
Length: 113 amino acids
Theoretical weight: 13.31 KDa
Source organism: Homo sapiens
Expression system: Escherichia coli
UniProt:
  • Canonical: Q15059 (Residues: 306-416; Coverage: 15%)
Gene names: BRD3, KIAA0043, RING3L
Sequence domains: Bromodomain

Ligands and Environments

1 bound ligand:
Ligand 79C 1 x 79C
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: RIGAKU MICROMAX-007 HF
Spacegroup: C2
Unit cell:
a: 55.58Å b: 63.27Å c: 40.04Å
α: 90° β: 109.99° γ: 90°
R-values:
R R work R free
0.153 0.152 0.182
Expression system: Escherichia coli

Quick links

Citations

3 citation in other articles

1,4-Dihydropyridinebutyrolactone-derived ring-opened ester and amide analogs targeting BET bromodomains.
Jiang et al. (2022)
2 more