7to7

BRD3-BD1 in complex with RaPID linear peptide 1xAcK.4XE (monoAcK.4xE)

Method: X-RAY DIFFRACTION Dmax: 118.7 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 heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 25–147 Chain B; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 1xAcK.4xE (monoAcK.4xE) × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M PCTP, pH 4.0, 25% w/v PEG1500 Resolution 1.93 Å R-free 0.251
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain D; UniProt 25–147 Chain E; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 1xAcK.4xE (monoAcK.4xE) × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M PCTP, pH 4.0, 25% w/v PEG1500 Resolution 1.93 Å R-free 0.251

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 6–128; UniProt 25–147 Author chain B; PDBConstruct 6–128; UniProt 25–147 Author chain D; PDBConstruct 6–128; UniProt 25–147 Author chain E; PDBConstruct 6–128; UniProt 25–147

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 7to7

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7to7
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7to7
Deposition date deposition_date2022-01-23
Structure title titleBRD3-BD1 in complex with RaPID linear peptide 1xAcK.4XE (monoAcK.4xE)
Keywords keywordsBET, bromodomain, RaPID, BRD3, acetylated, TRANSCRIPTION; TRANSCRIPTION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.93
Radius of gyration Rg (electron density) rg_electron29.93
Forward intensity I(0) i051322200.00
Molecular weight molecular_weight58373.0 kDa
Excluded volume excluded_volume73966 ų
Envelope volume envelope_volume98548 ų
Hydration-shell volume shell_volume28138 ų
Envelope diameter envelope_diameter124.0
Shell Rg shell_rg36.06
Envelope Rg envelope_rg29.82
Shape Rg shape_rg29.92
Total Rg total_rg30.62
Total atoms total_atoms4101
Residues n_residues486
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 dmax118.7
Rg (real space) rg_real30.97
Rg uncertainty (real space) rg_real_error1.38
I(0) (real space) i0_real5.1320e+07
I(0) uncertainty (real space) i0_real_error9.0190e+05
Rg (reciprocal space) rg_reciprocal30.95
I(0) (reciprocal space) i0_reciprocal51320000.0000
Solution quality estimate total_estimate0.8057
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary41.9
Skewness Skewness skewness0.314
Kurtosis Kurtosis kurtosis-0.195
Angular range angular_range— – 0.2550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6145000.0000
Real-space data points n_real_points52
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.575; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.746; Smooth: 0.999

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

CATH v4.4 (4 domains)

Domain ID domain_id7to7A01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology920 — Histone Acetyltransferase; Chain A
Homologous superfamily homologous superfamily10 — Bromodomain-like
Domain ID domain_id7to7B01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology920 — Histone Acetyltransferase; Chain A
Homologous superfamily homologous superfamily10 — Bromodomain-like
Domain ID domain_id7to7D01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology920 — Histone Acetyltransferase; Chain A
Homologous superfamily homologous superfamily10 — Bromodomain-like
Domain ID domain_id7to7E01
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)