1xtc

CHOLERA TOXIN

Method: X-RAY DIFFRACTION Dmax: 88.1 Å Quality: GOOD

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

CHOLERA TOXIN

OrganismNot specified

UniProt P01555

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 heterocomplex Heteromer Protein × 7 PDB declaration: heptameric(7) Consistent with protein copy count Chain A; UniProt 19–212 Chain C; UniProt 213–258 Not recorded CHOLERA TOXIN × 5 (P01556) X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.40 Å

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.

11 other PDB entries and 15 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CHTA_VIBCH
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–194; UniProt 19–212 Author chain C; PDBConstruct 1–46; UniProt 213–258

CHOLERA TOXIN

OrganismNot specified

UniProt P01556

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 heterocomplex Heteromer Protein × 7 PDB declaration: heptameric(7) Consistent with protein copy count Chain D; UniProt 22–124 Chain E; UniProt 22–124 Chain F; UniProt 22–124 Chain G; UniProt 22–124 Chain H; UniProt 22–124 Not recorded CHOLERA TOXIN × 1 (P01555) CHOLERA TOXIN × 1 (P01555) X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.40 Å

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 35 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CHTB_VIBCH
Isoform
PDB entities 3
Chains and sequence ranges Author chain D; PDBConstruct 1–103; UniProt 22–124 Author chain E; PDBConstruct 1–103; UniProt 22–124 Author chain F; PDBConstruct 1–103; UniProt 22–124 Author chain G; PDBConstruct 1–103; UniProt 22–124 Author chain H; PDBConstruct 1–103; UniProt 22–124

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 1xtc

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1xtc
Deposition date deposition_date1996-01-10
Structure title titleCHOLERA TOXIN
Keywords keywordsENTEROTOXIN, TOXIN; TOXIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.18
Radius of gyration Rg (electron density) rg_electron26.87
Forward intensity I(0) i0120871000.00
Molecular weight molecular_weight85276.0 kDa
Excluded volume excluded_volume106180 ų
Envelope volume envelope_volume125030 ų
Hydration-shell volume shell_volume37813 ų
Envelope diameter envelope_diameter92.4
Shell Rg shell_rg34.97
Envelope Rg envelope_rg26.98
Shape Rg shape_rg26.90
Total Rg total_rg27.55
Total atoms total_atoms5997
Residues n_residues752
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 dmax88.1
Rg (real space) rg_real28.01
Rg uncertainty (real space) rg_real_error0.64
I(0) (real space) i0_real1.2090e+08
I(0) uncertainty (real space) i0_real_error1.7220e+06
Rg (reciprocal space) rg_reciprocal28.06
I(0) (reciprocal space) i0_reciprocal120900000.0000
Solution quality estimate total_estimate0.8269
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary36.2
Skewness Skewness skewness0.151
Kurtosis Kurtosis kurtosis-0.514
Angular range angular_range— – 0.2800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha50540000.0000
Real-space data points n_real_points57
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.919; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.996; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 13 domains

SCOP 2.08 (6 domains)

Domain ID domain_idd1xtc.1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.166 — ADP-ribosylation
Superfamily Superfamily superfamilyd.166.1 — ADP-ribosylation
Family Family familyd.166.1.1 — ADP-ribosylating toxins
Domain ID domain_idd1xtcd_
Class classb — All beta proteins
Fold Fold foldb.40 — OB-fold
Superfamily Superfamily superfamilyb.40.2 — Bacterial enterotoxins
Family Family familyb.40.2.1 — Bacterial AB5 toxins, B-subunits
Domain ID domain_idd1xtce_
Class classb — All beta proteins
Fold Fold foldb.40 — OB-fold
Superfamily Superfamily superfamilyb.40.2 — Bacterial enterotoxins
Family Family familyb.40.2.1 — Bacterial AB5 toxins, B-subunits
Domain ID domain_idd1xtcf_
Class classb — All beta proteins
Fold Fold foldb.40 — OB-fold
Superfamily Superfamily superfamilyb.40.2 — Bacterial enterotoxins
Family Family familyb.40.2.1 — Bacterial AB5 toxins, B-subunits
Domain ID domain_idd1xtcg_
Class classb — All beta proteins
Fold Fold foldb.40 — OB-fold
Superfamily Superfamily superfamilyb.40.2 — Bacterial enterotoxins
Family Family familyb.40.2.1 — Bacterial AB5 toxins, B-subunits
Domain ID domain_idd1xtch_
Class classb — All beta proteins
Fold Fold foldb.40 — OB-fold
Superfamily Superfamily superfamilyb.40.2 — Bacterial enterotoxins
Family Family familyb.40.2.1 — Bacterial AB5 toxins, B-subunits

CATH v4.4 (7 domains)

Domain ID domain_id1xtcA00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology210 — Heat-Labile Enterotoxin; Chain A
Homologous superfamily homologous superfamily10 — Heat-Labile Enterotoxin, subunit A
Domain ID domain_id1xtcC00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology5 — Single alpha-helices involved in coiled-coils or other helix-helix interfaces
Homologous superfamily homologous superfamily240
Domain ID domain_id1xtcD00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily110
Domain ID domain_id1xtcE00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily110
Domain ID domain_id1xtcF00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily110
Domain ID domain_id1xtcG00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily110
Domain ID domain_id1xtcH00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily110

8. Citations (2)

9. Files and Curves (10)