2dpd

Crystal structure of the Replication Termination Protein in complex with a pseudosymmetric B-site

Method: X-RAY DIFFRACTION Dmax: 80.9 Å Quality: GOOD

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

Replication termination protein

Bacillus subtilis

UniProt P68732

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 Homooligomer Protein × 2 DNA 2 PDB declaration: tetrameric(4) Consistent with all polymer counts Chain A; UniProt 1–122 Chain B; UniProt 1–122 Mutation:C110S 5'-D(*CP*TP*AP*TP*GP*AP*AP*CP*AP*TP*AP*AP*TP*GP*TP*TP*CP*AP*TP*AP*G)-3' × 1 5'-D(*CP*TP*AP*TP*GP*AP*AP*CP*AP*TP*TP*AP*TP*GP*TP*TP*CP*AP*TP*AP*G)-3' × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.6;298 K;25% MPD, 75mM sodium acetate pH 4.6, 20mM calcium chloride, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 3.17 Å R-free 0.278

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.

6 other PDB entries and 10 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RTP_BACSU
Isoform
PDB entities 3
Chains and sequence ranges Author chain A; PDBConstruct 1–122; UniProt 1–122 Author chain B; PDBConstruct 1–122; UniProt 1–122

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 2dpd

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2dpd
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id2dpd
Deposition date deposition_date2006-05-09
Structure title titleCrystal structure of the Replication Termination Protein in complex with a pseudosymmetric B-site
Keywords keywordswinged-helix protein-DNA complex, Replication Termination, Fork Arrest Mechanism, DNA BINDING PROTEIN-DNA COMPLEX; DNA BINDING PROTEIN/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.47
Radius of gyration Rg (electron density) rg_electron22.92
Forward intensity I(0) i035909200.00
Molecular weight molecular_weight40370.0 kDa
Excluded volume excluded_volume47985 ų
Envelope volume envelope_volume59116 ų
Hydration-shell volume shell_volume22304 ų
Envelope diameter envelope_diameter85.2
Shell Rg shell_rg28.92
Envelope Rg envelope_rg23.12
Shape Rg shape_rg22.88
Total Rg total_rg23.68
Total atoms total_atoms2794
Residues n_residues274
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 dmax80.9
Rg (real space) rg_real23.54
Rg uncertainty (real space) rg_real_error0.71
I(0) (real space) i0_real3.5910e+07
I(0) uncertainty (real space) i0_real_error5.4470e+05
Rg (reciprocal space) rg_reciprocal23.52
I(0) (reciprocal space) i0_reciprocal35910000.0000
Solution quality estimate total_estimate0.7909
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary26.1
Skewness Skewness skewness0.438
Kurtosis Kurtosis kurtosis-0.223
Angular range angular_range— – 0.3400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4177000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.785; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.928; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd2dpda_
Class classa — All alpha proteins
Fold Fold folda.4 — DNA/RNA-binding 3-helical bundle
Superfamily Superfamily superfamilya.4.5 — 'Winged helix' DNA-binding domain
Family Family familya.4.5.7 — Replication terminator protein (RTP)
Domain ID domain_idd2dpdb_
Class classa — All alpha proteins
Fold Fold folda.4 — DNA/RNA-binding 3-helical bundle
Superfamily Superfamily superfamilya.4.5 — 'Winged helix' DNA-binding domain
Family Family familya.4.5.7 — Replication terminator protein (RTP)

CATH v4.4 (2 domains)

Domain ID domain_id2dpdA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily10 — Winged helix-like DNA-binding domain superfamily/Winged helix DNA-binding domain
Domain ID domain_id2dpdB00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology10 — Arc Repressor Mutant, subunit A
Homologous superfamily homologous superfamily10 — Winged helix-like DNA-binding domain superfamily/Winged helix DNA-binding domain

8. Citations (1)

9. Files and Curves (10)