1dk2

REFINED SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA

Method: SOLUTION NMR Dmax: 37.0 Å Quality: REASONABLE

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

DNA POLYMERASE BETA

Rattus norvegicus

UniProt P06766

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 1–86 Fragment:N-TERMINAL DOMAIN, RESIDUES 1-87 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.7;300 K;Ionic strength (raw mmCIF value) 400 mM NACL;Pressure AMBIENT NMR measurement conditions:pH 6.8;298 K;Ionic strength (raw mmCIF value) 100 mM NACL;Pressure AMBIENT NMR sample composition:2.8 MM RAT DNA POLYMERASE BETA N-TERMINAL DOMAIN (2-87) U-15N,13C; 5MM TRIS- D11; 400MM NACL NMR sample composition:2 MM RAT DNA POLYMERASE BETA N-TERMINAL DOMAIN (2-87) U-15N; 5MM TRIS-D11; 100MM NACL NMR sample composition:4 MM RAT DNA POLYMERASE BETA N-TERMINAL DOMAIN (2-87) U-15N; 5MM TRIS-D11; 400MM NACL NMR sample composition:2.8 MM RAT DNA POLYMERASE BETA N-TERMINAL DOMAIN (2-87) U-15N,13C; 5MM TRIS- D11; 400MM NACL NMR sample composition:1.4 MM RAT DNA POLYMERASE BETA N-TERMINAL DOMAIN (2-87); 5MM TRIS-D11; 400MM NACL Resolution not provided

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.

30 other PDB entries and 37 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DPOB_RAT
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–86; UniProt 1–86

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 1dk2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1dk2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1dk2
Deposition date deposition_date1999-12-06
Structure title titleREFINED SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA
Keywords keywords;DNA-BINDING, DEOXYRIBOSE 5'-PHOSPHATE LYASE, NUCLEOTIDYLTRANSFERASE, TRANSFERASE ;; TRANSFERASE
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier14.37
Radius of gyration Rg (electron density) rg_electron14.25
Forward intensity I(0) i0715700000.00
Molecular weight molecular_weight236830.0 kDa
Excluded volume excluded_volume302200 ų
Envelope volume envelope_volume45949 ų
Hydration-shell volume shell_volume19599 ų
Envelope diameter envelope_diameter71.3
Shell Rg shell_rg26.39
Envelope Rg envelope_rg20.59
Shape Rg shape_rg14.19
Total Rg total_rg14.78
Total atoms total_atoms34500
Residues n_residues2150
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 dmax37.0
Rg (real space) rg_real13.64
Rg uncertainty (real space) rg_real_error0.04
I(0) (real space) i0_real6.8240e+08
I(0) uncertainty (real space) i0_real_error4.8460e+06
Rg (reciprocal space) rg_reciprocal14.42
I(0) (reciprocal space) i0_reciprocal715700000.0000
Solution quality estimate total_estimate0.6854
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary15.9
Skewness Skewness skewness0.117
Kurtosis Kurtosis kurtosis-0.547
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha5.3860
Highest regularization parameter α highest_alpha92930.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.003; Oscil: 1.000; Stabil: 0.970; Sysdev: 0.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1dk2a_
Class classa — All alpha proteins
Fold Fold folda.60 — SAM domain-like
Superfamily Superfamily superfamilya.60.6 — DNA polymerase beta, N-terminal domain-like
Family Family familya.60.6.1 — DNA polymerase beta, N-terminal domain-like

CATH v4.4 (1 domains)

Domain ID domain_id1dk2A00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology150 — DNA polymerase; domain 1
Homologous superfamily homologous superfamily110 — DNA polymerase beta, N-terminal domain-like

8. Citations (3)

9. Files and Curves (10)