9au5

Ternary complex of human DNA polymerase theta polymerase domain with a cognate C:G base pair

Method: ELECTRON MICROSCOPY Dmax: 91.5 Å Quality: GOOD

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

DNA polymerase theta

Homo sapiens

UniProt O75417

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–DNA Monomer Protein × 1 DNA 2 PDB declaration: trimeric(3) Consistent with all polymer counts Chain A; UniProt 1792–2590 Not recorded ;DNA (5'-D(*AP*GP*CP*TP*CP*TP*AP*CP*GP*GP*AP*TP*GP*C)-3') ; × 1 ;DNA (5'-D(P*GP*CP*AP*TP*CP*CP*GP*TP*AP*GP*(2DA))-3') ; × 1 DGT 2'-DEOXYGUANOSINE-5'-TRIPHOSPHATE × 1 MG MAGNESIUM ION × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.6 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.11 Å

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.

32 other PDB entries and 57 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DPOLQ_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–799; UniProt 1792–2590

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 9au5

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9au5
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9au5
Deposition date deposition_date2024-02-28
Structure title titleTernary complex of human DNA polymerase theta polymerase domain with a cognate C:G base pair
Keywords keywordsDNA translesion synthesis, theta-mediated end joining, A-family DNA polymerase, DNA BINDING PROTEIN-DNA complex; DNA BINDING PROTEIN/DNA
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier27.54
Radius of gyration Rg (electron density) rg_electron27.01
Forward intensity I(0) i0114865000.00
Molecular weight molecular_weight79848.0 kDa
Excluded volume excluded_volume97938 ų
Envelope volume envelope_volume120540 ų
Hydration-shell volume shell_volume36455 ų
Envelope diameter envelope_diameter98.0
Shell Rg shell_rg35.07
Envelope Rg envelope_rg27.16
Shape Rg shape_rg27.02
Total Rg total_rg27.72
Total atoms total_atoms5577
Residues n_residues665
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 dmax91.5
Rg (real space) rg_real27.46
Rg uncertainty (real space) rg_real_error0.65
I(0) (real space) i0_real1.1490e+08
I(0) uncertainty (real space) i0_real_error1.7770e+06
Rg (reciprocal space) rg_reciprocal27.49
I(0) (reciprocal space) i0_reciprocal114900000.0000
Solution quality estimate total_estimate0.8827
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary33.1
Skewness Skewness skewness0.304
Kurtosis Kurtosis kurtosis-0.276
Angular range angular_range— – 0.2900 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha19540000.0000
Real-space data points n_real_points59
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.831; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.978

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)