8rzu

Structure of human SETD2 L1609P mutant in complex with SAM and H3K36M peptide

Method: X-RAY DIFFRACTION Dmax: 71.6 Å Quality: GOOD

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

Histone-lysine N-methyltransferase SETD2

Homo sapiens

UniProt Q9BYW2

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1433–1711 Mutation:L1609P Histone H3 × 1 (B2R6Y1) ZN ZINC ION × 3 SAM S-ADENOSYLMETHIONINE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;293 K;32% w/v PEG 4K, 100mM Tris, 800mM LiCl, pH 8.5 Resolution 2.19 Å R-free 0.264

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.

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

View Construct and Data Evidence
UniProt name SETD2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 17–295; UniProt 1433–1711

Histone H3

OrganismNot specified

UniProt B2R6Y1

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 30–43 Not recorded Histone-lysine N-methyltransferase SETD2 × 1 (Q9BYW2) ZN ZINC ION × 3 SAM S-ADENOSYLMETHIONINE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;293 K;32% w/v PEG 4K, 100mM Tris, 800mM LiCl, pH 8.5 Resolution 2.19 Å R-free 0.264

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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name B2R6Y1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–14; UniProt 30–43

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 8rzu

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8rzu
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8rzu
Deposition date deposition_date2024-02-13
Structure title titleStructure of human SETD2 L1609P mutant in complex with SAM and H3K36M peptide
Keywords keywordsHistone methyl-transferase, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier20.60
Radius of gyration Rg (electron density) rg_electron19.55
Forward intensity I(0) i018554800.00
Molecular weight molecular_weight30408.0 kDa
Excluded volume excluded_volume37143 ų
Envelope volume envelope_volume45328 ų
Hydration-shell volume shell_volume19630 ų
Envelope diameter envelope_diameter72.1
Shell Rg shell_rg25.90
Envelope Rg envelope_rg20.11
Shape Rg shape_rg19.49
Total Rg total_rg20.59
Total atoms total_atoms2109
Residues n_residues261
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 dmax71.6
Rg (real space) rg_real20.56
Rg uncertainty (real space) rg_real_error0.46
I(0) (real space) i0_real1.8550e+07
I(0) uncertainty (real space) i0_real_error2.2760e+05
Rg (reciprocal space) rg_reciprocal20.57
I(0) (reciprocal space) i0_reciprocal18550000.0000
Solution quality estimate total_estimate0.8726
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.9
Skewness Skewness skewness0.296
Kurtosis Kurtosis kurtosis-0.289
Angular range angular_range— – 0.3850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3213000.0000
Real-space data points n_real_points70
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.795; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.974; Smooth: 0.981

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (2)

9. Files and Curves (10)