8vzm

DNA Ligase 1 captured with pre-step 3 ligation at the rA:T nicksite

Method: X-RAY DIFFRACTION Dmax: 82.9 Å Quality: EXCELLENT

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

DNA ligase 1

Homo sapiens

UniProt P18858

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 3 PDB declaration: tetrameric(4) Consistent with all polymer counts Chain A; UniProt 261–918 Not recorded ;DNA/RNA (5'-D(*GP*CP*TP*GP*AP*TP*GP*CP*GP*T)-R(P*A)-3') ; × 1 ;DNA (5'-D(*GP*TP*CP*CP*GP*AP*CP*CP*AP*CP*GP*CP*AP*TP*CP*AP*GP*C)-3') ; × 1 ;DNA (5'-D(P*GP*TP*CP*GP*GP*AP*C)-3') ; × 1 AMP ADENOSINE MONOPHOSPHATE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.7;298.1 K;100 mM MES (pH 6.7), 100 mM lithium acetate, 16% (w/v) PEG3350 Resolution 2.51 Å R-free 0.233

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.

33 other PDB entries and 35 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DNLI1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–658; UniProt 261–918

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 8vzm

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8vzm
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id8vzm
Deposition date deposition_date2024-02-11
最后修订 last_revision2024-05-22
Structure title titleDNA Ligase 1 captured with pre-step 3 ligation at the rA:T nicksite
Keywords keywordsLIG1, DNA Ligase 1, LIGASE, Ligase-DNA complex; Ligase/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.00
Radius of gyration Rg (electron density) rg_electron26.38
Forward intensity I(0) i0125343000.00
Molecular weight molecular_weight81043.0 kDa
Excluded volume excluded_volume98459 ų
Envelope volume envelope_volume122800 ų
Hydration-shell volume shell_volume37596 ų
Envelope diameter envelope_diameter87.3
Shell Rg shell_rg34.84
Envelope Rg envelope_rg26.29
Shape Rg shape_rg26.40
Total Rg total_rg27.11
Total atoms total_atoms5666
Residues n_residues682
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 dmax82.9
Rg (real space) rg_real26.82
Rg uncertainty (real space) rg_real_error0.35
I(0) (real space) i0_real1.2530e+08
I(0) uncertainty (real space) i0_real_error1.6840e+06
Rg (reciprocal space) rg_reciprocal26.88
I(0) (reciprocal space) i0_reciprocal125300000.0000
Solution quality estimate total_estimate0.9045
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary33.7
Skewness Skewness skewness0.155
Kurtosis Kurtosis kurtosis-0.467
Angular range angular_range— – 0.2950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha21880000.0000
Real-space data points n_real_points60
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.924; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.989; Smooth: 0.992

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)