1crz

CRYSTAL STRUCTURE OF THE E. COLI TOLB PROTEIN

Method: X-RAY DIFFRACTION Dmax: 79.1 Å Quality: REASONABLE

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

TOLB PROTEIN

Escherichia coli

UniProt P0A855

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 28–430 Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;PEG 8000, SODIUM CHLORIDE, TRIS, TCEP, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 293.0K Resolution 1.95 Å R-free 0.238

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.

5 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TOLB_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–403; UniProt 28–430

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 1crz

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1crz
Deposition date deposition_date1999-08-16
Structure title titleCRYSTAL STRUCTURE OF THE E. COLI TOLB PROTEIN
Keywords keywordsTWO DOMAINS: BETA PROPELLER AND ALPHA/BETA FOLD, TOXIN BINDING PROTEIN; TOXIN BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.18
Radius of gyration Rg (electron density) rg_electron22.29
Forward intensity I(0) i033805700.00
Molecular weight molecular_weight43177.0 kDa
Excluded volume excluded_volume53281 ų
Envelope volume envelope_volume61303 ų
Hydration-shell volume shell_volume23412 ų
Envelope diameter envelope_diameter80.7
Shell Rg shell_rg28.87
Envelope Rg envelope_rg22.53
Shape Rg shape_rg22.29
Total Rg total_rg23.07
Total atoms total_atoms3030
Residues n_residues397
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 dmax79.1
Rg (real space) rg_real23.18
Rg uncertainty (real space) rg_real_error0.51
I(0) (real space) i0_real3.3810e+07
I(0) uncertainty (real space) i0_real_error4.4720e+05
Rg (reciprocal space) rg_reciprocal23.18
I(0) (reciprocal space) i0_reciprocal33810000.0000
Solution quality estimate total_estimate0.7131
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.8
Skewness Skewness skewness0.384
Kurtosis Kurtosis kurtosis-0.296
Angular range angular_range— – 0.3450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8096000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.799; Stabil: 1.000; Sysdev: 0.307; Positv: 1.000; Valcen: 0.972; Smooth: 0.977

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_idd1crza1
Class classb — All beta proteins
Fold Fold foldb.68 — 6-bladed beta-propeller
Superfamily Superfamily superfamilyb.68.4 — TolB, C-terminal domain
Family Family familyb.68.4.1 — TolB, C-terminal domain
Domain ID domain_idd1crza2
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.51 — Anticodon-binding domain-like
Superfamily Superfamily superfamilyc.51.2 — TolB, N-terminal domain
Family Family familyc.51.2.1 — TolB, N-terminal domain

CATH v4.4 (2 domains)

Domain ID domain_id1crzA01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily10070 — TolB, N-terminal domain
Domain ID domain_id1crzA02
Class class2 — Mainly Beta
Architecture architecture120 — 6 Propeller
Topology topology10 — Neuraminidase
Homologous superfamily homologous superfamily30 — TolB, C-terminal domain

8. Citations (2)

9. Files and Curves (10)