4ee2

Crystal Structure of Anthrax Protective Antigen K446M Mutant to 1.91-A Resolution

Method: X-RAY DIFFRACTION Dmax: 115.4 Å Quality: GOOD

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

Protective antigen

Bacillus anthracis

UniProt P13423

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 30–764 Fragment:Protective antigen Mutation:K446M CA CALCIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8;292 K;0.1M tris, 20% peg2k-MME, 0.2M TMAO, pH 8, VAPOR DIFFUSION, HANGING DROP, temperature 292K Resolution 1.91 Å R-free 0.265

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.

28 other PDB entries and 42 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PAG_BACAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–736; UniProt 30–764

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 4ee2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4ee2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4ee2
Deposition date deposition_date2012-03-28
Structure title titleCrystal Structure of Anthrax Protective Antigen K446M Mutant to 1.91-A Resolution
Keywords keywordsAnthrax Toxin, Cell-binding, Assembly, Channel formation, Protein translocation, TOXIN, TRANSPORT PROTEIN; TOXIN, TRANSPORT PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier33.20
Radius of gyration Rg (electron density) rg_electron32.92
Forward intensity I(0) i0101582000.00
Molecular weight molecular_weight78949.0 kDa
Excluded volume excluded_volume98314 ų
Envelope volume envelope_volume129370 ų
Hydration-shell volume shell_volume34468 ų
Envelope diameter envelope_diameter118.7
Shell Rg shell_rg37.53
Envelope Rg envelope_rg33.12
Shape Rg shape_rg32.93
Total Rg total_rg33.29
Total atoms total_atoms5562
Residues n_residues701
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 dmax115.4
Rg (real space) rg_real33.50
Rg uncertainty (real space) rg_real_error1.17
I(0) (real space) i0_real1.0160e+08
I(0) uncertainty (real space) i0_real_error1.8220e+06
Rg (reciprocal space) rg_reciprocal33.38
I(0) (reciprocal space) i0_reciprocal101600000.0000
Solution quality estimate total_estimate0.8461
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary31.3
Skewness Skewness skewness0.501
Kurtosis Kurtosis kurtosis-0.335
Angular range angular_range— – 0.2400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha32840000.0000
Real-space data points n_real_points49
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.770; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.762; Smooth: 0.923

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd4ee2a1
Class classf — Membrane and cell surface proteins and peptides
Fold Fold foldf.60 — Anthrax protective antigen C-terminal-like
Superfamily Superfamily superfamilyf.60.1 — Anthrax protective antigen C-terminal-like
Family Family familyf.60.1.1 — Anthrax protective antigen C-terminal-like
Domain ID domain_idd4ee2a2
Class classb — All beta proteins
Fold Fold foldb.179 — Anthrax protective antigen N-terminal-like
Superfamily Superfamily superfamilyb.179.1 — PA14-like
Family Family familyb.179.1.1 — PA14

CATH v4.4 (4 domains)

Domain ID domain_id4ee2A01
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology182 — Toxin - Anthrax Protective Antigen; domain 1
Homologous superfamily homologous superfamily10 — Toxin - Anthrax Protective Antigen;domain 1
Domain ID domain_id4ee2A02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily240 — Protective antigen, heptamerisation domain
Domain ID domain_id4ee2A03
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily110
Domain ID domain_id4ee2A04
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily810

8. Citations (1)

9. Files and Curves (10)