9klb

G9a in complex with RK-133232 (compound 16g)

Method: X-RAY DIFFRACTION Dmax: 103.9 Å Quality: GOOD

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

Histone-lysine N-methyltransferase EHMT2

Homo sapiens

UniProt Q96KQ7

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 913–1193 Chain B; UniProt 913–1193 Not recorded ZN ZINC ION × 8 SFG SINEFUNGIN × 2 A1L57 ~{N}-[(~{E},2~{S})-4-cyclopropyl-1-[(6-ethoxypyridin-3-yl)amino]-1-oxidanylidene-but-3-en-2-yl]-4-(pyridin-4-ylamino)benzamide × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;0.1M Bis-Tris propane (pH~7.5), 0.2M Sodium Formate or Fluoride, 10% Ethylene Glycol, ~25% PEG3350 Resolution 1.81 Å R-free 0.221

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.

34 other PDB entries and 55 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name EHMT2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–283; UniProt 913–1193 Author chain B; PDBConstruct 3–283; UniProt 913–1193

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 9klb

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9klb
Deposition date deposition_date2024-11-14
Structure title titleG9a in complex with RK-133232 (compound 16g)
Keywords keywordshistone lysine methyltransferase, inhibitor, protein-inhibitor complex, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.70
Radius of gyration Rg (electron density) rg_electron26.18
Forward intensity I(0) i0129588000.00
Molecular weight molecular_weight58640.0 kDa
Excluded volume excluded_volume55728 ų
Envelope volume envelope_volume95746 ų
Hydration-shell volume shell_volume30785 ų
Envelope diameter envelope_diameter110.6
Shell Rg shell_rg33.17
Envelope Rg envelope_rg26.58
Shape Rg shape_rg26.18
Total Rg total_rg26.68
Total atoms total_atoms4371
Residues n_residues532
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 dmax103.9
Rg (real space) rg_real26.79
Rg uncertainty (real space) rg_real_error0.95
I(0) (real space) i0_real1.2960e+08
I(0) uncertainty (real space) i0_real_error1.9430e+06
Rg (reciprocal space) rg_reciprocal26.76
I(0) (reciprocal space) i0_reciprocal129600000.0000
Solution quality estimate total_estimate0.7878
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary31.7
Skewness Skewness skewness0.524
Kurtosis Kurtosis kurtosis0.146
Angular range angular_range— – 0.2950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10140000.0000
Real-space data points n_real_points60
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.503; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.734; Smooth: 0.995

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)