7o45

Crystal structure of ADD domain of the human DNMT3B methyltransferase

Method: X-RAY DIFFRACTION Dmax: 74.9 Å Quality: EXCELLENT

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

Isoform 6 of DNA (cytosine-5)-methyltransferase 3B

Homo sapiens

UniProt Q9UBC3

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 404–546 Chain B; UniProt 404–546 Chain C; UniProt 404–546 Not recorded ZN ZINC ION × 9 BR BROMIDE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;288 K;0.2M NaBr; 0.1M bis-tris-propane pH 7.5; 20% PEG 3350 Resolution 2.10 Å R-free 0.228
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain D; UniProt 404–546 Not recorded ZN ZINC ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;288 K;0.2M NaBr; 0.1M bis-tris-propane pH 7.5; 20% PEG 3350 Resolution 2.10 Å R-free 0.228

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.

45 other PDB entries and 54 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DNM3B_HUMAN
Isoform Q9UBC3-6
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–146; UniProt 404–546 Author chain B; PDBConstruct 4–146; UniProt 404–546 Author chain C; PDBConstruct 4–146; UniProt 404–546 Author chain D; PDBConstruct 4–146; UniProt 404–546

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 7o45

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7o45
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7o45
Deposition date deposition_date2021-04-05
Structure title titleCrystal structure of ADD domain of the human DNMT3B methyltransferase
Keywords keywordsMethyltransferase 3B, DNA methylation, DNMT3B, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.18
Radius of gyration Rg (electron density) rg_electron24.04
Forward intensity I(0) i066859100.00
Molecular weight molecular_weight57305.0 kDa
Excluded volume excluded_volume68834 ų
Envelope volume envelope_volume88226 ų
Hydration-shell volume shell_volume30030 ų
Envelope diameter envelope_diameter76.5
Shell Rg shell_rg31.88
Envelope Rg envelope_rg24.13
Shape Rg shape_rg24.03
Total Rg total_rg24.91
Total atoms total_atoms3912
Residues n_residues507
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 dmax74.9
Rg (real space) rg_real25.02
Rg uncertainty (real space) rg_real_error0.33
I(0) (real space) i0_real6.6860e+07
I(0) uncertainty (real space) i0_real_error8.3520e+05
Rg (reciprocal space) rg_reciprocal25.07
I(0) (reciprocal space) i0_reciprocal66860000.0000
Solution quality estimate total_estimate0.9110
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary34.5
Skewness Skewness skewness0.038
Kurtosis Kurtosis kurtosis-0.615
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha12740000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.961; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.991; Smooth: 0.966

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)