9mpk

BRD3-BD1 in complex with cyclic peptide 2.1C-Y5A

Method: X-RAY DIFFRACTION Dmax: 114.9 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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 2.1C-Y5A × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M Sodium citrate pH 5.5, 20 % w/v PEG 3000 Resolution 2.70 Å R-free 0.295
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 2.1C-Y5A × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M Sodium citrate pH 5.5, 20 % w/v PEG 3000 Resolution 2.70 Å R-free 0.295
3 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 2.1C-Y5A × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M Sodium citrate pH 5.5, 20 % w/v PEG 3000 Resolution 2.70 Å R-free 0.295
4 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 2.1C-Y5A × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M Sodium citrate pH 5.5, 20 % w/v PEG 3000 Resolution 2.70 Å R-free 0.295
5 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain E; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 2.1C-Y5A × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M Sodium citrate pH 5.5, 20 % w/v PEG 3000 Resolution 2.70 Å R-free 0.295
6 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain F; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 2.1C-Y5A × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.1 M Sodium citrate pH 5.5, 20 % w/v PEG 3000 Resolution 2.70 Å R-free 0.295

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 96 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 C; PDBConstruct 6–128; UniProt 25–147 Author chain D; PDBConstruct 6–128; UniProt 25–147 Author chain E; PDBConstruct 6–128; UniProt 25–147 Author chain F; 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 9mpk

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9mpk
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9mpk
Deposition date deposition_date2024-12-30
最后修订 last_revision2026-04-08
Structure title titleBRD3-BD1 in complex with cyclic peptide 2.1C-Y5A
Keywords keywordsBRD2, BRD3, cyclic peptide, GENE REGULATION; GENE REGULATION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier34.77
Radius of gyration Rg (electron density) rg_electron34.34
Forward intensity I(0) i0124770000.00
Molecular weight molecular_weight92189.0 kDa
Excluded volume excluded_volume116600 ų
Envelope volume envelope_volume163620 ų
Hydration-shell volume shell_volume41352 ų
Envelope diameter envelope_diameter119.8
Shell Rg shell_rg39.30
Envelope Rg envelope_rg33.73
Shape Rg shape_rg34.32
Total Rg total_rg34.82
Total atoms total_atoms6483
Residues n_residues760
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 dmax114.9
Rg (real space) rg_real34.75
Rg uncertainty (real space) rg_real_error1.25
I(0) (real space) i0_real1.2480e+08
I(0) uncertainty (real space) i0_real_error2.2550e+06
Rg (reciprocal space) rg_reciprocal34.77
I(0) (reciprocal space) i0_reciprocal124800000.0000
Solution quality estimate total_estimate0.8840
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary42.5
Skewness Skewness skewness0.305
Kurtosis Kurtosis kurtosis-0.274
Angular range angular_range— – 0.2300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6596000.0000
Real-space data points n_real_points47
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.860; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.907

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)