9kn9

NSD2-PWWP1 domain bound with compound 1.

Method: X-RAY DIFFRACTION Dmax: 58.4 Å Quality: EXCELLENT

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

Histone-lysine N-methyltransferase NSD2

Homo sapiens

UniProt O96028

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 217–349 Chain B; UniProt 217–349 Not recorded SO4 SULFATE ION × 3 A1EF6 (Z)-N-methyl-3-sulfanyl-prop-2-enamide × 2 EPE 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;291.15 K;2.5 M ammonium sulfate, 0.01 M magnesium chloride, 0.1 M HEPES (pH 7.0), and 40% (v/v) tert-butanol Resolution 2.00 Å R-free 0.275

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.

21 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NSD2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–133; UniProt 217–349 Author chain B; PDBConstruct 1–133; UniProt 217–349

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 9kn9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9kn9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9kn9
Deposition date deposition_date2024-11-18
Structure title titleNSD2-PWWP1 domain bound with compound 1.
Keywords keywordsPWWP, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.48
Radius of gyration Rg (electron density) rg_electron18.56
Forward intensity I(0) i026694800.00
Molecular weight molecular_weight26983.0 kDa
Excluded volume excluded_volume26415 ų
Envelope volume envelope_volume43653 ų
Hydration-shell volume shell_volume19629 ų
Envelope diameter envelope_diameter59.6
Shell Rg shell_rg24.84
Envelope Rg envelope_rg18.64
Shape Rg shape_rg18.51
Total Rg total_rg19.34
Total atoms total_atoms2042
Residues n_residues256
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 dmax58.4
Rg (real space) rg_real19.36
Rg uncertainty (real space) rg_real_error0.26
I(0) (real space) i0_real2.6690e+07
I(0) uncertainty (real space) i0_real_error2.9940e+05
Rg (reciprocal space) rg_reciprocal19.38
I(0) (reciprocal space) i0_reciprocal26700000.0000
Solution quality estimate total_estimate0.9118
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.7
Skewness Skewness skewness0.150
Kurtosis Kurtosis kurtosis-0.530
Angular range angular_range— – 0.4100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6148000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.957; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.995; Smooth: 0.983

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)