4el4

Crystal structure of the catalytic domain of botulinum neurotoxin BoNT/A C134S/C165S double mutant

Method: X-RAY DIFFRACTION Dmax: 71.7 Å Quality: EXCELLENT

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

Botulinum neurotoxin A light 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 1–425 Fragment:UNP residues 1-425 Mutation:C134S, C165S ZN ZINC ION × 1 GOL GLYCEROL × 2 IMD IMIDAZOLE × 2 EDO 1,2-ETHANEDIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6;293 K;reservoir: 29% MPEG2K, 0.04 M Li2SO4, 0.1 M imidazole-HCl pH 6.0, cryoprotectant: 18% MPEG2K, 22% MPD, 10% DMSO, 0.050 M bicine, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 293.0K Resolution 1.20 Å R-free 0.202

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 21–445; UniProt 1–425

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 4el4

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4el4
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4el4
Deposition date deposition_date2012-04-10
Structure title titleCrystal structure of the catalytic domain of botulinum neurotoxin BoNT/A C134S/C165S double mutant
Keywords keywordsMetalloprotease, peptidase M27 superfamily, Clostridial neurotoxin zinc protease, Human target snap-25, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.93
Radius of gyration Rg (electron density) rg_electron21.83
Forward intensity I(0) i037853900.00
Molecular weight molecular_weight49095.0 kDa
Excluded volume excluded_volume62052 ų
Envelope volume envelope_volume71791 ų
Hydration-shell volume shell_volume26780 ų
Envelope diameter envelope_diameter72.2
Shell Rg shell_rg29.24
Envelope Rg envelope_rg22.05
Shape Rg shape_rg21.79
Total Rg total_rg22.86
Total atoms total_atoms3471
Residues n_residues425
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 dmax71.7
Rg (real space) rg_real22.82
Rg uncertainty (real space) rg_real_error0.34
I(0) (real space) i0_real3.7850e+07
I(0) uncertainty (real space) i0_real_error4.9150e+05
Rg (reciprocal space) rg_reciprocal22.85
I(0) (reciprocal space) i0_reciprocal37850000.0000
Solution quality estimate total_estimate0.9014
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.7
Skewness Skewness skewness0.204
Kurtosis Kurtosis kurtosis-0.389
Angular range angular_range— – 0.3450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8239000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.909; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.992; Smooth: 0.995

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd4el4a_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.92 — Zincin-like
Superfamily Superfamily superfamilyd.92.1 — Metalloproteases ('zincins'), catalytic domain
Family Family familyd.92.1.7 — Clostridium neurotoxins, catalytic domain

CATH v4.4 (1 domains)

Domain ID domain_id4el4A00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1240 — Zincin-like
Homologous superfamily homologous superfamily10 — Metalloproteases ("zincins"), catalytic domain like

8. Citations (1)

9. Files and Curves (10)