3qw6

Crystal structure of the protease domain of Botulinum Neurotoxin Serotype A with a peptide inhibitor RYGC

Method: X-RAY DIFFRACTION Dmax: 71.2 Å Quality: EXCELLENT

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

Botulinum neurotoxin type A

Clostridium botulinum

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 1–424 Fragment:light chain (UNP residues 1-424) inhibitory peptide RYGC × 1 ZN ZINC ION × 1 SO4 SULFATE ION × 3 NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.9;293 K;22% PEG3350, 0.3 M ammonium sulfate, pH 6.9, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 1.60 Å R-free 0.222

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 1–424; UniProt 1–424

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 3qw6

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3qw6
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id3qw6
Deposition date deposition_date2011-02-26
Structure title titleCrystal structure of the protease domain of Botulinum Neurotoxin Serotype A with a peptide inhibitor RYGC
Keywords keywords;endopeptidase, syntaxin, bio-warfare agent, membrane, metal-binding, metalloprotease, protease, secreted, transmembrane, SNAP25, HYDROLASE-HYDROLASE INHIBITOR complex ;; HYDROLASE/HYDROLASE INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.77
Radius of gyration Rg (electron density) rg_electron21.71
Forward intensity I(0) i038628200.00
Molecular weight molecular_weight49128.0 kDa
Excluded volume excluded_volume61876 ų
Envelope volume envelope_volume71395 ų
Hydration-shell volume shell_volume26703 ų
Envelope diameter envelope_diameter73.2
Shell Rg shell_rg29.21
Envelope Rg envelope_rg22.04
Shape Rg shape_rg21.68
Total Rg total_rg22.70
Total atoms total_atoms3466
Residues n_residues426
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 dmax71.2
Rg (real space) rg_real22.66
Rg uncertainty (real space) rg_real_error0.38
I(0) (real space) i0_real3.8630e+07
I(0) uncertainty (real space) i0_real_error5.0400e+05
Rg (reciprocal space) rg_reciprocal22.69
I(0) (reciprocal space) i0_reciprocal38630000.0000
Solution quality estimate total_estimate0.9001
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.0
Skewness Skewness skewness0.214
Kurtosis Kurtosis kurtosis-0.384
Angular range angular_range— – 0.3500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8710000.0000
Real-space data points n_real_points67
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: 0.990; Smooth: 0.981

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_idd3qw6a_
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_id3qw6A00
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)