7lb4

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

Method: X-RAY DIFFRACTION Dmax: 60.9 Å Quality: EXCELLENT

1. Protein Identity and Related Structures Protein Identity & Related Structures

Bromodomain-containing protein 3

Homo sapiens

UniProt Q15059

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 306–416 Not recorded BMF Bromosporine × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M HEPES pH 7.5, 10 % w/v Polyethylene glycol 6,000, 5 % v/v (+/-)-2-Methyl-2,4-pentanediol Resolution 2.00 Å R-free 0.229
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 306–416 Not recorded BMF Bromosporine × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M HEPES pH 7.5, 10 % w/v Polyethylene glycol 6,000, 5 % v/v (+/-)-2-Methyl-2,4-pentanediol Resolution 2.00 Å R-free 0.229

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

47 other PDB entries and 100 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BRD3_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–113; UniProt 306–416 Author chain B; PDBConstruct 3–113; UniProt 306–416

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 7lb4

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7lb4
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7lb4
Deposition date deposition_date2021-01-07
Structure title titleCrystal structure of the second bromodomain (BD2) of human BRD3 bound to bromosporine
Keywords keywordsBET, ERK5, dual BRD-kinase inhibitor, GENE REGULATION, GENE REGULATION-INHIBITOR complex; GENE REGULATION/INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier19.65
Radius of gyration Rg (electron density) rg_electron18.71
Forward intensity I(0) i012793700.00
Molecular weight molecular_weight26342.0 kDa
Excluded volume excluded_volume32745 ų
Envelope volume envelope_volume39288 ų
Hydration-shell volume shell_volume17855 ų
Envelope diameter envelope_diameter61.8
Shell Rg shell_rg24.45
Envelope Rg envelope_rg18.64
Shape Rg shape_rg18.71
Total Rg total_rg19.58
Total atoms total_atoms1848
Residues n_residues216
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax60.9
Rg (real space) rg_real19.53
Rg uncertainty (real space) rg_real_error0.34
I(0) (real space) i0_real1.2790e+07
I(0) uncertainty (real space) i0_real_error1.4670e+05
Rg (reciprocal space) rg_reciprocal19.55
I(0) (reciprocal space) i0_reciprocal12790000.0000
Solution quality estimate total_estimate0.9077
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.9
Skewness Skewness skewness0.126
Kurtosis Kurtosis kurtosis-0.581
Angular range angular_range— – 0.4050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4149000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.937; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.986

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd7lb4a_
Class classa — All alpha proteins
Fold Fold folda.29 — Bromodomain-like
Superfamily Superfamily superfamilya.29.2 — Bromodomain
Family Family familya.29.2.0 — automated matches
Domain ID domain_idd7lb4b_
Class classa — All alpha proteins
Fold Fold folda.29 — Bromodomain-like
Superfamily Superfamily superfamilya.29.2 — Bromodomain
Family Family familya.29.2.0 — automated matches

8. Citations (1)

9. Files and Curves (10)