6g3p

X-ray structure of seleno-methionine labelled NSD3-PWWP1

Method: X-RAY DIFFRACTION Dmax: 94.4 Å Quality: REASONABLE

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

Histone-lysine N-methyltransferase NSD3

Homo sapiens

UniProt Q9BZ95

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 247–398 Fragment:UNP residues 247-398 Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;293 K;50 mM TRIS pH 9.0, 23% PEG3350 Resolution 2.80 Å R-free 0.262
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 247–398 Fragment:UNP residues 247-398 Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;293 K;50 mM TRIS pH 9.0, 23% PEG3350 Resolution 2.80 Å R-free 0.262
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 247–398 Fragment:UNP residues 247-398 Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;293 K;50 mM TRIS pH 9.0, 23% PEG3350 Resolution 2.80 Å R-free 0.262
4 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain D; UniProt 247–398 Fragment:UNP residues 247-398 Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;293 K;50 mM TRIS pH 9.0, 23% PEG3350 Resolution 2.80 Å R-free 0.262

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.

24 other PDB entries and 29 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NSD3_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–153; UniProt 247–398 Author chain B; PDBConstruct 2–153; UniProt 247–398 Author chain C; PDBConstruct 2–153; UniProt 247–398 Author chain D; PDBConstruct 2–153; UniProt 247–398

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 6g3p

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6g3p
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6g3p
Deposition date deposition_date2018-03-26
Structure title titleX-ray structure of seleno-methionine labelled NSD3-PWWP1
Keywords keywordsInhibitor, PWWP domain, ONCOPROTEIN; ONCOPROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.42
Radius of gyration Rg (electron density) rg_electron27.74
Forward intensity I(0) i055670400.00
Molecular weight molecular_weight57082.0 kDa
Excluded volume excluded_volume70854 ų
Envelope volume envelope_volume93454 ų
Hydration-shell volume shell_volume28635 ų
Envelope diameter envelope_diameter99.9
Shell Rg shell_rg34.32
Envelope Rg envelope_rg27.81
Shape Rg shape_rg27.71
Total Rg total_rg28.51
Total atoms total_atoms4014
Residues n_residues465
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 dmax94.4
Rg (real space) rg_real28.45
Rg uncertainty (real space) rg_real_error0.71
I(0) (real space) i0_real5.5670e+07
I(0) uncertainty (real space) i0_real_error9.0800e+05
Rg (reciprocal space) rg_reciprocal28.44
I(0) (reciprocal space) i0_reciprocal55670000.0000
Solution quality estimate total_estimate0.7171
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.7
Skewness Skewness skewness0.299
Kurtosis Kurtosis kurtosis-0.508
Angular range angular_range— – 0.2800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha11840000.0000
Real-space data points n_real_points57
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.901; Stabil: 1.000; Sysdev: 0.242; Positv: 1.000; Valcen: 0.934; Smooth: 0.953

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)