9knb

NSD2-PWWP1 domain bound with compound 9

Method: X-RAY DIFFRACTION Dmax: 50.9 Å Quality: REASONABLE

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 217–349 Not recorded EPE 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 A1EF7 N-(2-methoxyphenyl)-2-selanyl-benzamide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;292 K;0.2 M sodium formate and 20% (m/v) PEG3350 Resolution 1.84 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

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 9knb

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9knb
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id9knb
Deposition date deposition_date2024-11-18
Structure title titleNSD2-PWWP1 domain bound with compound 9
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_guinier15.18
Radius of gyration Rg (electron density) rg_electron14.18
Forward intensity I(0) i06666700.00
Molecular weight molecular_weight13085.0 kDa
Excluded volume excluded_volume12890 ų
Envelope volume envelope_volume19752 ų
Hydration-shell volume shell_volume11976 ų
Envelope diameter envelope_diameter49.8
Shell Rg shell_rg19.84
Envelope Rg envelope_rg14.63
Shape Rg shape_rg14.19
Total Rg total_rg15.09
Total atoms total_atoms990
Residues n_residues125
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 dmax50.9
Rg (real space) rg_real15.12
Rg uncertainty (real space) rg_real_error0.30
I(0) (real space) i0_real6.6670e+06
I(0) uncertainty (real space) i0_real_error6.7950e+04
Rg (reciprocal space) rg_reciprocal15.12
I(0) (reciprocal space) i0_reciprocal6667000.0000
Solution quality estimate total_estimate0.7316
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary18.0
Skewness Skewness skewness0.261
Kurtosis Kurtosis kurtosis-0.291
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1344000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.811; Stabil: 1.000; Sysdev: 0.368; Positv: 1.000; Valcen: 0.991; Smooth: 0.978

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)