6elg

Tryptophan Repressor TrpR from E.coli variant M42F T44L T81I S88Y with Indole-3-acetonitrile

Method: X-RAY DIFFRACTION Dmax: 63.5 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 A; UniProt 1–108 Chain B; UniProt 1–108 Not recorded 3BO 1H-indol-3-ylacetonitrile × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;0.2 M Ammonium Formate 20% PEG 3350 Resolution 1.38 Å R-free 0.176

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 A; PDBConstruct 1–108; UniProt 1–108 Author chain B; PDBConstruct 1–108; UniProt 1–108

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 6elg

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6elg
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6elg
Deposition date deposition_date2017-09-28
Structure title titleTryptophan Repressor TrpR from E.coli variant M42F T44L T81I S88Y with Indole-3-acetonitrile
Keywords keywordsLigand Binding, TRANSCRIPTION; TRANSCRIPTION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier20.10
Radius of gyration Rg (electron density) rg_electron18.72
Forward intensity I(0) i010606400.00
Molecular weight molecular_weight24479.0 kDa
Excluded volume excluded_volume30899 ų
Envelope volume envelope_volume37981 ų
Hydration-shell volume shell_volume17380 ų
Envelope diameter envelope_diameter64.7
Shell Rg shell_rg24.49
Envelope Rg envelope_rg19.05
Shape Rg shape_rg18.66
Total Rg total_rg19.84
Total atoms total_atoms3482
Residues n_residues209
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 dmax63.5
Rg (real space) rg_real20.03
Rg uncertainty (real space) rg_real_error0.48
I(0) (real space) i0_real1.0610e+07
I(0) uncertainty (real space) i0_real_error1.4740e+05
Rg (reciprocal space) rg_reciprocal20.05
I(0) (reciprocal space) i0_reciprocal10610000.0000
Solution quality estimate total_estimate0.8166
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.5
Skewness Skewness skewness0.195
Kurtosis Kurtosis kurtosis-0.462
Angular range angular_range— – 0.3950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1372000.0000
Real-space data points n_real_points71
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.872; Stabil: 0.999; 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 (3)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd6elga_
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_idd6elgb_
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_id6elgA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1270 — Trp Operon Repressor; Chain A
Homologous superfamily homologous superfamily10 — TrpR-like
Domain ID domain_id6elgB00
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)