21hj

Solution structures of BRD9 bromodomain in complex with histone H3 lactyl-lysine 18 (H3K18la) peptide

Method: SOLUTION NMR Dmax: 69.0 Å Quality: REASONABLE

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

Bromodomain-containing protein 9

Homo sapiens

UniProt Q9H8M2

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 134–250 Not recorded Histone H3.3C × 1 (Q6NXT2) SOLUTION NMR NMR measurement conditions:pH 7.4;298 K;Ionic strength (raw mmCIF value) null;Pressure 1 NMR sample composition:500 mM sodium chloride, 2.7 mM potassium chloride, 10 mM sodium phosphate, 1.8 mM potassium phosphate, 2 mM DTT, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:500 mM sodium chloride, 2.7 mM potassium chloride, 10 mM sodium phosphate, 1.8 mM potassium phosphate, 2 mM DTT, 100% D2O | 100% D2O Resolution not provided

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.

50 other PDB entries and 73 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BRD9_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–117; UniProt 134–250

Histone H3.3C

OrganismNot specified

UniProt Q6NXT2

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 B; UniProt 12–26 Non-standard monomer:Yes (specific site not provided by mmCIF) Bromodomain-containing protein 9 × 1 (Q9H8M2) SOLUTION NMR NMR measurement conditions:pH 7.4;298 K;Ionic strength (raw mmCIF value) null;Pressure 1 NMR sample composition:500 mM sodium chloride, 2.7 mM potassium chloride, 10 mM sodium phosphate, 1.8 mM potassium phosphate, 2 mM DTT, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:500 mM sodium chloride, 2.7 mM potassium chloride, 10 mM sodium phosphate, 1.8 mM potassium phosphate, 2 mM DTT, 100% D2O | 100% D2O Resolution not provided

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.

22 other PDB entries and 26 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name H3C_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–15; UniProt 12–26

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 21hj

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 21hj
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id21hj
Deposition date deposition_date2025-12-12
最后修订 last_revision2026-03-11
Structure title titleSolution structures of BRD9 bromodomain in complex with histone H3 lactyl-lysine 18 (H3K18la) peptide
Keywords keywords;histone lactylation, BRD9, chromatin remodeling, chromatin accessibility, transcription regulation, hepatocellular carcinoma, PROTEIN BINDING ;; PROTEIN BINDING
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier17.08
Radius of gyration Rg (electron density) rg_electron16.60
Forward intensity I(0) i01173550000.00
Molecular weight molecular_weight298870.0 kDa
Excluded volume excluded_volume377590 ų
Envelope volume envelope_volume48556 ų
Hydration-shell volume shell_volume19658 ų
Envelope diameter envelope_diameter76.1
Shell Rg shell_rg27.49
Envelope Rg envelope_rg21.98
Shape Rg shape_rg16.59
Total Rg total_rg16.87
Total atoms total_atoms42200
Residues n_residues2620
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 dmax69.0
Rg (real space) rg_real17.21
Rg uncertainty (real space) rg_real_error0.67
I(0) (real space) i0_real1.1740e+09
I(0) uncertainty (real space) i0_real_error1.4470e+07
Rg (reciprocal space) rg_reciprocal17.20
I(0) (reciprocal space) i0_reciprocal1174000000.0000
Solution quality estimate total_estimate0.6493
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary17.2
Skewness Skewness skewness0.606
Kurtosis Kurtosis kurtosis0.216
Angular range angular_range— – 0.4650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha655000.0000
Real-space data points n_real_points77
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.336; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.430; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)