1wrs

NMR STUDY OF HOLO TRP REPRESSOR

Method: SOLUTION NMR Dmax: 77.3 Å Quality: REASONABLE

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

HOLO 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 TRP TRYPTOPHAN × 2 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 1wrs

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1wrs
Deposition date deposition_date1995-05-12
Structure title titleNMR STUDY OF HOLO TRP REPRESSOR
Keywords keywordsOPERON REPRESSOR, TRANSCRIPTION REGULATION, DNA-BINDING, COMPLEX (OPERON REPRESSOR-PEPTIDE) COMPLEX; COMPLEX (OPERON REPRESSOR/PEPTIDE)
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier20.08
Radius of gyration Rg (electron density) rg_electron19.53
Forward intensity I(0) i01855430000.00
Molecular weight molecular_weight362850.0 kDa
Excluded volume excluded_volume454650 ų
Envelope volume envelope_volume98203 ų
Hydration-shell volume shell_volume32120 ų
Envelope diameter envelope_diameter86.7
Shell Rg shell_rg32.95
Envelope Rg envelope_rg25.38
Shape Rg shape_rg19.47
Total Rg total_rg20.04
Total atoms total_atoms51480
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 dmax77.3
Rg (real space) rg_real20.06
Rg uncertainty (real space) rg_real_error0.65
I(0) (real space) i0_real1.8550e+09
I(0) uncertainty (real space) i0_real_error2.6890e+07
Rg (reciprocal space) rg_reciprocal20.07
I(0) (reciprocal space) i0_reciprocal1855000000.0000
Solution quality estimate total_estimate0.7231
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary23.2
Skewness Skewness skewness0.353
Kurtosis Kurtosis kurtosis-0.226
Angular range angular_range— – 0.3950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2845000.0000
Real-space data points n_real_points71
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.511; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.863; 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_idd1wrsr_
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_idd1wrss_
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_id1wrsR00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1270 — Trp Operon Repressor; Chain A
Homologous superfamily homologous superfamily10 — TrpR-like
Domain ID domain_id1wrsS00
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)