5l21

Crystal structure of BoNT/A receptor binding domain in complex with VHH C2

Method: X-RAY DIFFRACTION Dmax: 83.8 Å Quality: EXCELLENT

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

Botulinum neurotoxin type A

Clostridium botulinum (strain Hall / ATCC 3502 / NCTC 13319 / Type A)

UniProt A5HZZ9

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 872–1296 Mutation:T1158A VHH-C2 × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;291 K;18% polyethylene glycol 6,000; 100 mM Sodium Acetate, pH 5.0 Resolution 1.68 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.

22 other PDB entries and 25 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BXA1_CLOBH
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–428; UniProt 872–1296

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 5l21

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5l21
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5l21
Deposition date deposition_date2016-07-29
Structure title titleCrystal structure of BoNT/A receptor binding domain in complex with VHH C2
Keywords keywordsNeutralizing antibody; VHH; Botulinum neurotoxin; BoNT-A-VHH complex, TOXIN; TOXIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.50
Radius of gyration Rg (electron density) rg_electron25.25
Forward intensity I(0) i064590700.00
Molecular weight molecular_weight62897.0 kDa
Excluded volume excluded_volume78801 ų
Envelope volume envelope_volume93356 ų
Hydration-shell volume shell_volume30819 ų
Envelope diameter envelope_diameter86.7
Shell Rg shell_rg32.59
Envelope Rg envelope_rg25.46
Shape Rg shape_rg25.20
Total Rg total_rg26.17
Total atoms total_atoms4437
Residues n_residues544
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 dmax83.8
Rg (real space) rg_real26.43
Rg uncertainty (real space) rg_real_error0.54
I(0) (real space) i0_real6.4590e+07
I(0) uncertainty (real space) i0_real_error9.3580e+05
Rg (reciprocal space) rg_reciprocal26.45
I(0) (reciprocal space) i0_reciprocal64590000.0000
Solution quality estimate total_estimate0.9063
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary29.3
Skewness Skewness skewness0.232
Kurtosis Kurtosis kurtosis-0.527
Angular range angular_range— – 0.3000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha14810000.0000
Real-space data points n_real_points61
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.930; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.988

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 7 domains

SCOP 2.08 (4 domains)

Domain ID domain_idd5l21a1
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_idd5l21a2
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_idd5l21a3
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags
Domain ID domain_idd5l21b_
Class classb — All beta proteins
Fold Fold foldb.1 — Immunoglobulin-like beta-sandwich
Superfamily Superfamily superfamilyb.1.1 — Immunoglobulin
Family Family familyb.1.1.1 — V set domains (antibody variable domain-like)

CATH v4.4 (3 domains)

Domain ID domain_id5l21A01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily200
Domain ID domain_id5l21A02
Class class2 — Mainly Beta
Architecture architecture80 — Trefoil
Topology topology10 — Trefoil (Acidic Fibroblast Growth Factor, subunit A)
Homologous superfamily homologous superfamily50
Domain ID domain_id5l21B00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins

8. Citations (1)

9. Files and Curves (10)