6g5k

Crystal structure of the binding domain of Botulinum Neurotoxin type B in complex with human synaptotagmin 1

Method: X-RAY DIFFRACTION Dmax: 137.4 Å Quality: REASONABLE

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

Botulinum neurotoxin type B

Clostridium botulinum

UniProt P10844

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 857–1291 Not recorded Synaptotagmin-1 × 1 (P21579) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;294 K;0.1 M Amino acids 0.1 M Buffer System 2 7.5 50 % v/v Precipitant Mix 1 Resolution 2.00 Å R-free 0.235
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 857–1291 Not recorded Synaptotagmin-1 × 1 (P21579) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;294 K;0.1 M Amino acids 0.1 M Buffer System 2 7.5 50 % v/v Precipitant Mix 1 Resolution 2.00 Å R-free 0.235

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.

33 other PDB entries and 45 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BXB_CLOBO
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 25–459; UniProt 857–1291 Author chain B; PDBConstruct 25–459; UniProt 857–1291

Synaptotagmin-1

OrganismNot specified

UniProt P21579

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 C; UniProt 33–53 Not recorded Botulinum neurotoxin type B × 1 (P10844) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;294 K;0.1 M Amino acids 0.1 M Buffer System 2 7.5 50 % v/v Precipitant Mix 1 Resolution 2.00 Å R-free 0.235
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain 33; UniProt 33–53 Not recorded Botulinum neurotoxin type B × 1 (P10844) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;294 K;0.1 M Amino acids 0.1 M Buffer System 2 7.5 50 % v/v Precipitant Mix 1 Resolution 2.00 Å R-free 0.235

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.

21 other PDB entries and 30 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SYT1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain 33; PDBConstruct 1–21; UniProt 33–53 Author chain C; PDBConstruct 1–21; UniProt 33–53

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 6g5k

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6g5k
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6g5k
Deposition date deposition_date2018-03-29
Structure title titleCrystal structure of the binding domain of Botulinum Neurotoxin type B in complex with human synaptotagmin 1
Keywords keywordsbotulinum toxin, neurotoxin, protein engineering, receptor binding, TOXIN; TOXIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier38.66
Radius of gyration Rg (electron density) rg_electron39.13
Forward intensity I(0) i0156831000.00
Molecular weight molecular_weight105260.0 kDa
Excluded volume excluded_volume133130 ų
Envelope volume envelope_volume172280 ų
Hydration-shell volume shell_volume39342 ų
Envelope diameter envelope_diameter143.8
Shell Rg shell_rg41.30
Envelope Rg envelope_rg39.05
Shape Rg shape_rg39.13
Total Rg total_rg39.27
Total atoms total_atoms7455
Residues n_residues876
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 dmax137.4
Rg (real space) rg_real39.19
Rg uncertainty (real space) rg_real_error1.55
I(0) (real space) i0_real1.5680e+08
I(0) uncertainty (real space) i0_real_error2.9820e+06
Rg (reciprocal space) rg_reciprocal38.87
I(0) (reciprocal space) i0_reciprocal156800000.0000
Solution quality estimate total_estimate0.5948
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.1
Skewness Skewness skewness0.587
Kurtosis Kurtosis kurtosis-0.198
Angular range angular_range— – 0.2050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha48990000.0000
Real-space data points n_real_points42
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.682; Stabil: 1.000; Sysdev: 0.132; Positv: 1.000; Valcen: 0.667; Smooth: 0.620

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)