7mev

Human Apex/Ref1 monomer with C138A mutation

Method: X-RAY DIFFRACTION Dmax: 55.0 Å Quality: GOOD

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

DNA-(apurinic or apyrimidinic site) endonuclease, mitochondrial

Homo sapiens

UniProt P27695

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 44–318 Mutation:C138A MG MAGNESIUM ION × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8;277.15 K;20 %w/v PEG 3350, 200 mM Sodium nitrate Resolution 1.60 Å R-free 0.196

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.

66 other PDB entries and 123 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name APEX1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–276; UniProt 44–318

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 7mev

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id7mev
Deposition date deposition_date2021-04-07
Structure title titleHuman Apex/Ref1 monomer with C138A mutation
Keywords keywordsHuman Apex/Ref1, DNA BINDING PROTEIN, DNase I, metal ion binding; DNA BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.56
Radius of gyration Rg (electron density) rg_electron17.38
Forward intensity I(0) i016653400.00
Molecular weight molecular_weight31254.0 kDa
Excluded volume excluded_volume39285 ų
Envelope volume envelope_volume43371 ų
Hydration-shell volume shell_volume20055 ų
Envelope diameter envelope_diameter55.8
Shell Rg shell_rg24.38
Envelope Rg envelope_rg17.73
Shape Rg shape_rg17.34
Total Rg total_rg18.49
Total atoms total_atoms2205
Residues n_residues275
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 dmax55.0
Rg (real space) rg_real18.40
Rg uncertainty (real space) rg_real_error0.20
I(0) (real space) i0_real1.6650e+07
I(0) uncertainty (real space) i0_real_error1.7220e+05
Rg (reciprocal space) rg_reciprocal18.42
I(0) (reciprocal space) i0_reciprocal16650000.0000
Solution quality estimate total_estimate0.8986
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary54.2
Skewness Skewness skewness0.041
Kurtosis Kurtosis kurtosis-0.508
Angular range angular_range— – 0.4300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4366000.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.932; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.967; Smooth: 0.914

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)