9mph

BRD3-BD1 in complex with cyclic peptide 4.1D

Method: X-RAY DIFFRACTION Dmax: 92.5 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 D; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 4.1D × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.2 M lithium chloride pH 6.8, 20% (w/v) PEG3350 Resolution 2.25 Å R-free 0.249
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 25–147 Chain C; UniProt 25–147 Fragment:BD1 (UNP residues 25-147) 4.1D × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;291 K;0.2 M lithium chloride pH 6.8, 20% (w/v) PEG3350 Resolution 2.25 Å R-free 0.249

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 C; PDBConstruct 6–128; UniProt 25–147 Author chain D; 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 9mph

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9mph
Deposition date deposition_date2024-12-30
最后修订 last_revision2026-04-08
Structure title titleBRD3-BD1 in complex with cyclic peptide 4.1D
Keywords keywordsBRD3, 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_guinier27.18
Radius of gyration Rg (electron density) rg_electron26.67
Forward intensity I(0) i055995300.00
Molecular weight molecular_weight60407.0 kDa
Excluded volume excluded_volume76428 ų
Envelope volume envelope_volume93269 ų
Hydration-shell volume shell_volume29842 ų
Envelope diameter envelope_diameter101.1
Shell Rg shell_rg33.00
Envelope Rg envelope_rg27.00
Shape Rg shape_rg26.67
Total Rg total_rg27.35
Total atoms total_atoms4243
Residues n_residues500
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 dmax92.5
Rg (real space) rg_real27.26
Rg uncertainty (real space) rg_real_error0.72
I(0) (real space) i0_real5.6000e+07
I(0) uncertainty (real space) i0_real_error8.1560e+05
Rg (reciprocal space) rg_reciprocal27.24
I(0) (reciprocal space) i0_reciprocal55990000.0000
Solution quality estimate total_estimate0.7981
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary30.3
Skewness Skewness skewness0.441
Kurtosis Kurtosis kurtosis-0.219
Angular range angular_range— – 0.2900 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha15750000.0000
Real-space data points n_real_points59
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.804; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.960; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)