2vua

Crystal Structure of the Botulinum Neurotoxin Serotype A binding domain

Method: X-RAY DIFFRACTION Dmax: 83.2 Å Quality: GOOD

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

BOTULINUM NEUROTOXIN A HEAVY CHAIN

CLOSTRIDIUM BOTULINUM

UniProt P10845

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 876–1296 Fragment:BINDING DOMAIN, RESIDUES 876-1296 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.2;18% PEG3350, 0.2 M MGCL2, 0.1 M BISTRIS PH 5.2 Resolution 1.70 Å R-free 0.205

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 41 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BXA1_CLOBO
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 23–443; UniProt 876–1296

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 2vua

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2vua
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2vua
Deposition date deposition_date2008-05-22
Structure title titleCrystal Structure of the Botulinum Neurotoxin Serotype A binding domain
Keywords keywordsGANGLIOSIDE, RECEPTOR, TOXIN, MEMBRANE, SECRETED, METAL-BINDING, HYDROLASE, METALLOPROTEASE, NEUROTOXIN, PROTEASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.06
Radius of gyration Rg (electron density) rg_electron23.92
Forward intensity I(0) i040775400.00
Molecular weight molecular_weight49558.0 kDa
Excluded volume excluded_volume62155 ų
Envelope volume envelope_volume73041 ų
Hydration-shell volume shell_volume25866 ų
Envelope diameter envelope_diameter87.1
Shell Rg shell_rg30.73
Envelope Rg envelope_rg24.11
Shape Rg shape_rg23.86
Total Rg total_rg24.93
Total atoms total_atoms3486
Residues n_residues422
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 dmax83.2
Rg (real space) rg_real25.10
Rg uncertainty (real space) rg_real_error0.64
I(0) (real space) i0_real4.0780e+07
I(0) uncertainty (real space) i0_real_error6.1030e+05
Rg (reciprocal space) rg_reciprocal25.09
I(0) (reciprocal space) i0_reciprocal40780000.0000
Solution quality estimate total_estimate0.8794
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.8
Skewness Skewness skewness0.422
Kurtosis Kurtosis kurtosis-0.318
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8405000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.830; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.948; Smooth: 0.988

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 5 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd2vuaa1
Class classb — All beta proteins
Fold Fold foldb.29 — Concanavalin A-like lectins/glucanases
Superfamily Superfamily superfamilyb.29.1 — Concanavalin A-like lectins/glucanases
Family Family familyb.29.1.6 — Clostridium neurotoxins, the second last domain
Domain ID domain_idd2vuaa2
Class classb — All beta proteins
Fold Fold foldb.42 — beta-Trefoil
Superfamily Superfamily superfamilyb.42.4 — STI-like
Family Family familyb.42.4.2 — Clostridium neurotoxins, C-terminal domain
Domain ID domain_idd2vuaa3
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (2 domains)

Domain ID domain_id2vuaA01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily200
Domain ID domain_id2vuaA02
Class class2 — Mainly Beta
Architecture architecture80 — Trefoil
Topology topology10 — Trefoil (Acidic Fibroblast Growth Factor, subunit A)
Homologous superfamily homologous superfamily50

8. Citations (1)

9. Files and Curves (10)