1bnp

NMR SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA, 55 STRUCTURES

Method: SOLUTION NMR Dmax: 41.4 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 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 2–87; 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 1bnp

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1bnp
Deposition date deposition_date1996-04-25
Structure title titleNMR SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA, 55 STRUCTURES
Keywords keywordsN-TERMINAL DOMAIN, DNA POLYMERASE BETA, SINGLE-STRANDED DNA-BINDING, NUCLEOTIDYLTRANSFERASE, NUCLEOTIDYLTRANSFERASE (DNA-BINDING); NUCLEOTIDYLTRANSFERASE (DNA-BINDING)
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier15.45
Radius of gyration Rg (electron density) rg_electron15.36
Forward intensity I(0) i03545450000.00
Molecular weight molecular_weight529180.0 kDa
Excluded volume excluded_volume674420 ų
Envelope volume envelope_volume76748 ų
Hydration-shell volume shell_volume27133 ų
Envelope diameter envelope_diameter72.7
Shell Rg shell_rg30.83
Envelope Rg envelope_rg23.95
Shape Rg shape_rg15.26
Total Rg total_rg15.99
Total atoms total_atoms77000
Residues n_residues4785
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 dmax41.4
Rg (real space) rg_real14.56
Rg uncertainty (real space) rg_real_error0.06
I(0) (real space) i0_real3.3750e+09
I(0) uncertainty (real space) i0_real_error2.7570e+07
Rg (reciprocal space) rg_reciprocal15.57
I(0) (reciprocal space) i0_reciprocal3545000000.0000
Solution quality estimate total_estimate0.6771
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary15.2
Skewness Skewness skewness0.304
Kurtosis Kurtosis kurtosis-0.447
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha4.8300
Highest regularization parameter α highest_alpha283000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.004; Oscil: 0.953; Stabil: 0.981; 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_idd1bnpa_
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_id1bnpA00
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 (2)

9. Files and Curves (10)