6g5f

Crystal structure of an engineered Botulinum Neurotoxin type B mutant E1191M/S1199Y in complex with human synaptotagmin 1

Method: X-RAY DIFFRACTION Dmax: 142.6 Å Quality: GOOD

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1–1291 Chain B; UniProt 1–1291 Mutation:E231Q, H234Y Synaptotagmin-1 × 1 (P21579) GOL GLYCEROL × 3 MLI MALONATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;294 K;1.1 M sodium malonate dibasic monohydrate, HEPES pH 7.0, 0.5% v/v Jeffamine ED-2003 Resolution 2.50 Å R-free 0.232

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 46 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 1–1291; UniProt 1–1291 Author chain B; PDBConstruct 1–1291; UniProt 1–1291

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain P; UniProt 33–53 Not recorded Botulinum neurotoxin type B × 2 (P10844) GOL GLYCEROL × 3 MLI MALONATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;294 K;1.1 M sodium malonate dibasic monohydrate, HEPES pH 7.0, 0.5% v/v Jeffamine ED-2003 Resolution 2.50 Å R-free 0.232

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 31 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 P; 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 6g5f

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6g5f
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6g5f
Deposition date deposition_date2018-03-29
Structure title titleCrystal structure of an engineered Botulinum Neurotoxin type B mutant E1191M/S1199Y 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_guinier41.37
Radius of gyration Rg (electron density) rg_electron41.27
Forward intensity I(0) i0321245000.00
Molecular weight molecular_weight151570.0 kDa
Excluded volume excluded_volume191640 ų
Envelope volume envelope_volume256750 ų
Hydration-shell volume shell_volume53411 ų
Envelope diameter envelope_diameter154.0
Shell Rg shell_rg44.74
Envelope Rg envelope_rg41.12
Shape Rg shape_rg41.29
Total Rg total_rg41.43
Total atoms total_atoms10708
Residues n_residues1303
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 dmax142.6
Rg (real space) rg_real41.55
Rg uncertainty (real space) rg_real_error1.34
I(0) (real space) i0_real3.2120e+08
I(0) uncertainty (real space) i0_real_error5.7050e+06
Rg (reciprocal space) rg_reciprocal41.37
I(0) (reciprocal space) i0_reciprocal321200000.0000
Solution quality estimate total_estimate0.8583
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary41.3
Skewness Skewness skewness0.469
Kurtosis Kurtosis kurtosis-0.265
Angular range angular_range— – 0.1900 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha62120000.0000
Real-space data points n_real_points39
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.825; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.961; Smooth: 0.719

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id6g5fA00
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)