3ssw

E. coli trp aporepressor

Method: X-RAY DIFFRACTION Dmax: 62.3 Å Quality: GOOD

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

Trp operon repressor

Escherichia coli

UniProt P0A881

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain N; UniProt 2–108 Chain R; UniProt 2–108 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.5;294 K;Hampton Research Crystal Screen condition #6: 30% (w/v) PEG 4000, 200 mM MgCl2, 100 mM Tris HCl pH 8.5, VAPOR DIFFUSION, HANGING DROP, temperature 294K Resolution 1.67 Å R-free 0.219

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.

26 other PDB entries and 34 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TRPR_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain N; PDBConstruct 1–107; UniProt 2–108 Author chain R; PDBConstruct 1–107; UniProt 2–108

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 3ssw

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3ssw
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3ssw
Deposition date deposition_date2011-07-08
Structure title titleE. coli trp aporepressor
Keywords keywordsHelix-turn-Helix motif, DNA binding, trp operator, DNA BINDING PROTEIN; DNA BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.40
Radius of gyration Rg (electron density) rg_electron18.10
Forward intensity I(0) i09606240.00
Molecular weight molecular_weight22684.0 kDa
Excluded volume excluded_volume28416 ų
Envelope volume envelope_volume34616 ų
Hydration-shell volume shell_volume16496 ų
Envelope diameter envelope_diameter63.8
Shell Rg shell_rg23.69
Envelope Rg envelope_rg18.37
Shape Rg shape_rg18.07
Total Rg total_rg19.10
Total atoms total_atoms1596
Residues n_residues199
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 dmax62.3
Rg (real space) rg_real19.33
Rg uncertainty (real space) rg_real_error0.38
I(0) (real space) i0_real9.6060e+06
I(0) uncertainty (real space) i0_real_error1.1920e+05
Rg (reciprocal space) rg_reciprocal19.34
I(0) (reciprocal space) i0_reciprocal9606000.0000
Solution quality estimate total_estimate0.8073
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.6
Skewness Skewness skewness0.249
Kurtosis Kurtosis kurtosis-0.373
Angular range angular_range— – 0.4100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1565000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.832; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3sswn_
Class classa — All alpha proteins
Fold Fold folda.4 — DNA/RNA-binding 3-helical bundle
Superfamily Superfamily superfamilya.4.12 — TrpR-like
Family Family familya.4.12.1 — Trp repressor, TrpR
Domain ID domain_idd3sswr_
Class classa — All alpha proteins
Fold Fold folda.4 — DNA/RNA-binding 3-helical bundle
Superfamily Superfamily superfamilya.4.12 — TrpR-like
Family Family familya.4.12.1 — Trp repressor, TrpR

CATH v4.4 (2 domains)

Domain ID domain_id3sswN00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1270 — Trp Operon Repressor; Chain A
Homologous superfamily homologous superfamily10 — TrpR-like
Domain ID domain_id3sswR00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1270 — Trp Operon Repressor; Chain A
Homologous superfamily homologous superfamily10 — TrpR-like

8. Citations (1)

9. Files and Curves (10)