1n6a

Structure of SET7/9

Method: X-RAY DIFFRACTION Dmax: 72.8 Å Quality: REASONABLE

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

SET domain-containing protein 7

Homo sapiens

UniProt Q8WTS6

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 108–366 Fragment:residues 108-366 Non-standard monomer:Yes (specific site not provided by mmCIF) SAM S-ADENOSYLMETHIONINE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8;277 K;PEG6000, Tris-HCl, DTT, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 277K Resolution 1.70 Å R-free 0.217

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.

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

View Construct and Data Evidence
UniProt name SET7_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–259; UniProt 108–366

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 1n6a

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1n6a
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1n6a
Deposition date deposition_date2002-11-09
Structure title titleStructure of SET7/9
Keywords keywordsPROTEIN-LIGAND COMPLEX, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.78
Radius of gyration Rg (electron density) rg_electron18.77
Forward intensity I(0) i013717300.00
Molecular weight molecular_weight26725.0 kDa
Excluded volume excluded_volume32860 ų
Envelope volume envelope_volume38571 ų
Hydration-shell volume shell_volume17624 ų
Envelope diameter envelope_diameter71.9
Shell Rg shell_rg24.84
Envelope Rg envelope_rg19.39
Shape Rg shape_rg18.78
Total Rg total_rg19.66
Total atoms total_atoms1861
Residues n_residues228
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 dmax72.8
Rg (real space) rg_real19.81
Rg uncertainty (real space) rg_real_error0.54
I(0) (real space) i0_real1.3720e+07
I(0) uncertainty (real space) i0_real_error1.6700e+05
Rg (reciprocal space) rg_reciprocal19.81
I(0) (reciprocal space) i0_reciprocal13720000.0000
Solution quality estimate total_estimate0.7467
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary71.8
Skewness Skewness skewness0.454
Kurtosis Kurtosis kurtosis-0.058
Angular range angular_range— – 0.4000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2926000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.621; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.842; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1n6aa1
Class classb — All beta proteins
Fold Fold foldb.76 — open-sided beta-meander
Superfamily Superfamily superfamilyb.76.2 — Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain
Family Family familyb.76.2.1 — Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain
Domain ID domain_idd1n6aa2
Class classb — All beta proteins
Fold Fold foldb.85 — beta-clip
Superfamily Superfamily superfamilyb.85.7 — SET domain
Family Family familyb.85.7.1 — Histone lysine methyltransferases

CATH v4.4 (2 domains)

Domain ID domain_id1n6aA01
Class class2 — Mainly Beta
Architecture architecture20 — Single Sheet
Topology topology110 — Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain
Homologous superfamily homologous superfamily10 — Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain
Domain ID domain_id1n6aA02
Class class2 — Mainly Beta
Architecture architecture170 — Beta Complex
Topology topology270 — Beta-clip-like
Homologous superfamily homologous superfamily10 — SET domain

8. Citations (1)

9. Files and Curves (10)