5f2p

Crystal structure of the BRD9 bromodomain in complex with compound 3.

Method: X-RAY DIFFRACTION Dmax: 85.9 Å Quality: REASONABLE

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

BRD9

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 14–134 Fragment:bromodomain 5TY 2-(dimethylamino)-6-methyl-pyrido[4,3-d]pyrimidin-5-one × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.3;277 K;glycerol ethoxylate, Tris Resolution 1.80 Å R-free 0.220
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 14–134 Fragment:bromodomain 5TY 2-(dimethylamino)-6-methyl-pyrido[4,3-d]pyrimidin-5-one × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.3;277 K;glycerol ethoxylate, Tris Resolution 1.80 Å R-free 0.220

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 72 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BRD9_HUMAN
Isoform Q9H8M2-1
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–123; UniProt 14–134 Author chain B; PDBConstruct 3–123; UniProt 14–134

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 5f2p

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5f2p
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5f2p
Deposition date deposition_date2015-12-02
Structure title titleCrystal structure of the BRD9 bromodomain in complex with compound 3.
Keywords keywordsBromodomain, Inhibitor, REGULATORY PROTEINS, transcription; TRANSCRIPTION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.23
Radius of gyration Rg (electron density) rg_electron23.05
Forward intensity I(0) i011775300.00
Molecular weight molecular_weight26517.0 kDa
Excluded volume excluded_volume33614 ų
Envelope volume envelope_volume40718 ų
Hydration-shell volume shell_volume16602 ų
Envelope diameter envelope_diameter87.2
Shell Rg shell_rg27.43
Envelope Rg envelope_rg23.46
Shape Rg shape_rg23.08
Total Rg total_rg23.64
Total atoms total_atoms1860
Residues n_residues226
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 dmax85.9
Rg (real space) rg_real23.58
Rg uncertainty (real space) rg_real_error0.85
I(0) (real space) i0_real1.1780e+07
I(0) uncertainty (real space) i0_real_error1.7350e+05
Rg (reciprocal space) rg_reciprocal23.50
I(0) (reciprocal space) i0_reciprocal11770000.0000
Solution quality estimate total_estimate0.7388
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary19.8
Skewness Skewness skewness0.669
Kurtosis Kurtosis kurtosis-0.088
Angular range angular_range— – 0.3400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4945000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.452; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.346; Smooth: 0.897

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd5f2pa_
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_idd5f2pb_
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 (2 domains)

Domain ID domain_id5f2pA00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology920 — Histone Acetyltransferase; Chain A
Homologous superfamily homologous superfamily10 — Bromodomain-like
Domain ID domain_id5f2pB00
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)