1wrt

NMR STUDY OF APO TRP REPRESSOR

Method: SOLUTION NMR Dmax: 54.5 Å Quality: REASONABLE

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

APO TRP REPRESSOR

OrganismNot specified

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 3–107 Chain S; UniProt 3–107 Not recorded No other associated polymer SOLUTION NMR mmCIF provides none of the parsed experimental conditions 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.

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 1–105; UniProt 3–107 Author chain S; PDBConstruct 1–105; UniProt 3–107

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 1wrt

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1wrt
Deposition date deposition_date1995-05-12
Structure title titleNMR STUDY OF APO TRP REPRESSOR
Keywords keywordsOPERON REPRESSOR, TRANSCRIPTION REGULATION, DNA-BINDING; OPERON REPRESSOR
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier20.57
Radius of gyration Rg (electron density) rg_electron19.93
Forward intensity I(0) i01805970000.00
Molecular weight molecular_weight356720.0 kDa
Excluded volume excluded_volume446660 ų
Envelope volume envelope_volume103100 ų
Hydration-shell volume shell_volume32709 ų
Envelope diameter envelope_diameter98.4
Shell Rg shell_rg33.91
Envelope Rg envelope_rg26.52
Shape Rg shape_rg19.88
Total Rg total_rg20.44
Total atoms total_atoms50700
Residues n_residues3120
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 dmax54.5
Rg (real space) rg_real19.70
Rg uncertainty (real space) rg_real_error0.07
I(0) (real space) i0_real1.7230e+09
I(0) uncertainty (real space) i0_real_error1.5610e+07
Rg (reciprocal space) rg_reciprocal20.59
I(0) (reciprocal space) i0_reciprocal1806000000.0000
Solution quality estimate total_estimate0.6807
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary22.9
Skewness Skewness skewness0.263
Kurtosis Kurtosis kurtosis-0.429
Angular range angular_range— – 0.3850 −1
Current regularization parameter α current_alpha3.8080
Highest regularization parameter α highest_alpha2753000.0000
Real-space data points n_real_points70
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.001; Oscil: 0.983; Stabil: 0.968; Sysdev: 0.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1wrtr_
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_idd1wrts_
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_id1wrtR00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1270 — Trp Operon Repressor; Chain A
Homologous superfamily homologous superfamily10 — TrpR-like
Domain ID domain_id1wrtS00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1270 — Trp Operon Repressor; Chain A
Homologous superfamily homologous superfamily10 — TrpR-like

8. Citations (6)

9. Files and Curves (10)