1mi7

Crystal Structure of Domain Swapped trp Aporepressor in 30%(v/v) Isopropanol

Method: X-RAY DIFFRACTION Dmax: 99.0 Å Quality: REASONABLE

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 R; UniProt 1–107 Not recorded IPA ISOPROPYL ALCOHOL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;295 K;100 mM Na HEPES, 100 mM sodium chloride, 30%(v/v) isopropanol, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 2.50 Å R-free 0.288

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 R; PDBConstruct 1–107; UniProt 1–107

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 1mi7

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1mi7
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1mi7
Deposition date deposition_date2002-08-22
Structure title titleCrystal Structure of Domain Swapped trp Aporepressor in 30%(v/v) Isopropanol
Keywords keywordsDOMAIN SWAPPING, DNA BINDING PROTEIN, ALCOHOL INDUCED CONFORMATIONAL REARRANGEMENT, TRANSCRIPTION; TRANSCRIPTION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier29.53
Radius of gyration Rg (electron density) rg_electron30.39
Forward intensity I(0) i02621450.00
Molecular weight molecular_weight11863.0 kDa
Excluded volume excluded_volume14860 ų
Envelope volume envelope_volume27168 ų
Hydration-shell volume shell_volume9104 ų
Envelope diameter envelope_diameter95.8
Shell Rg shell_rg30.80
Envelope Rg envelope_rg29.43
Shape Rg shape_rg30.42
Total Rg total_rg30.34
Total atoms total_atoms834
Residues n_residues103
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 dmax99.0
Rg (real space) rg_real30.08
Rg uncertainty (real space) rg_real_error1.07
I(0) (real space) i0_real2.6210e+06
I(0) uncertainty (real space) i0_real_error3.9860e+04
Rg (reciprocal space) rg_reciprocal29.85
I(0) (reciprocal space) i0_reciprocal2621000.0000
Solution quality estimate total_estimate0.6114
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary27.5
Skewness Skewness skewness0.459
Kurtosis Kurtosis kurtosis-0.758
Angular range angular_range— – 0.2700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha92120.0000
Real-space data points n_real_points55
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.248; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.201; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1mi7r_
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 (1 domains)

Domain ID domain_id1mi7R00
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)