5a7c

Crystal structure of the second bromodomain of human BRD3 in complex with compound

Method: X-RAY DIFFRACTION Dmax: 92.8 Å Quality: GOOD

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 Fragment:BROMO 2 DOMAIN, RESIDUES 306-416 5D4 N-(6-ACETAMIDOHEXYL)ACETAMIDE × 1 EDO 1,2-ETHANEDIOL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;19% PEG 6000, 0.1M HEPES PH 7.0 Resolution 1.90 Å R-free 0.256
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 306–416 Fragment:BROMO 2 DOMAIN, RESIDUES 306-416 5D4 N-(6-ACETAMIDOHEXYL)ACETAMIDE × 1 EDO 1,2-ETHANEDIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;19% PEG 6000, 0.1M HEPES PH 7.0 Resolution 1.90 Å R-free 0.256
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 306–416 Fragment:BROMO 2 DOMAIN, RESIDUES 306-416 5D4 N-(6-ACETAMIDOHEXYL)ACETAMIDE × 1 EDO 1,2-ETHANEDIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;19% PEG 6000, 0.1M HEPES PH 7.0 Resolution 1.90 Å R-free 0.256
4 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain D; UniProt 306–416 Fragment:BROMO 2 DOMAIN, RESIDUES 306-416 5D4 N-(6-ACETAMIDOHEXYL)ACETAMIDE × 1 EDO 1,2-ETHANEDIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;19% PEG 6000, 0.1M HEPES PH 7.0 Resolution 1.90 Å R-free 0.256

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 98 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 Author chain C; PDBConstruct 3–113; UniProt 306–416 Author chain D; 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 5a7c

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5a7c
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5a7c
Deposition date deposition_date2015-07-03
Structure title titleCrystal structure of the second bromodomain of human BRD3 in complex with compound
Keywords keywordsDNA BINDING PROTEIN, BRD3, BROMODOMAIN CONTAINING PROTEIN 3, RING3-LIKE PROTEIN, BRD3 DOMAIN 2; DNA BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.99
Radius of gyration Rg (electron density) rg_electron27.48
Forward intensity I(0) i046345800.00
Molecular weight molecular_weight53135.0 kDa
Excluded volume excluded_volume66541 ų
Envelope volume envelope_volume82610 ų
Hydration-shell volume shell_volume26389 ų
Envelope diameter envelope_diameter96.3
Shell Rg shell_rg33.18
Envelope Rg envelope_rg27.52
Shape Rg shape_rg27.48
Total Rg total_rg28.10
Total atoms total_atoms3726
Residues n_residues441
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 dmax92.8
Rg (real space) rg_real28.19
Rg uncertainty (real space) rg_real_error0.78
I(0) (real space) i0_real4.6350e+07
I(0) uncertainty (real space) i0_real_error7.0300e+05
Rg (reciprocal space) rg_reciprocal28.13
I(0) (reciprocal space) i0_reciprocal46340000.0000
Solution quality estimate total_estimate0.8671
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.7
Skewness Skewness skewness0.477
Kurtosis Kurtosis kurtosis-0.386
Angular range angular_range— – 0.2850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8255000.0000
Real-space data points n_real_points58
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.838; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.887; Smooth: 0.869

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 9 domains

SCOP 2.08 (5 domains)

Domain ID domain_idd5a7ca1
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_idd5a7ca2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags
Domain ID domain_idd5a7cb_
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_idd5a7cc_
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_idd5a7cd_
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

CATH v4.4 (4 domains)

Domain ID domain_id5a7cA00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology920 — Histone Acetyltransferase; Chain A
Homologous superfamily homologous superfamily10 — Bromodomain-like
Domain ID domain_id5a7cB00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology920 — Histone Acetyltransferase; Chain A
Homologous superfamily homologous superfamily10 — Bromodomain-like
Domain ID domain_id5a7cC00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology920 — Histone Acetyltransferase; Chain A
Homologous superfamily homologous superfamily10 — Bromodomain-like
Domain ID domain_id5a7cD00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology920 — Histone Acetyltransferase; Chain A
Homologous superfamily homologous superfamily10 — Bromodomain-like

8. Citations (1)

9. Files and Curves (10)