8d4s

Crystal Structure of Cathepsin G Inhibited by Eap1 from S. aureus

Method: X-RAY DIFFRACTION Dmax: 139.2 Å Quality: GOOD

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

Cathepsin G, C-terminal truncated form

OrganismNot specified

UniProt P08311

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 21–243 Not recorded Extracellular Adherence Protein × 1 (Q99QS1) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;0.1M BisTris (pH 5.5), 0.2M Magnesium Chloride, 25% (w/v) PEG-3350 Resolution 1.95 Å R-free 0.261
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 21–243 Not recorded Extracellular Adherence Protein × 1 (Q99QS1) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;0.1M BisTris (pH 5.5), 0.2M Magnesium Chloride, 25% (w/v) PEG-3350 Resolution 1.95 Å R-free 0.261
3 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain E; UniProt 21–243 Not recorded Extracellular Adherence Protein × 1 (Q99QS1) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;0.1M BisTris (pH 5.5), 0.2M Magnesium Chloride, 25% (w/v) PEG-3350 Resolution 1.95 Å R-free 0.261
4 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain G; UniProt 21–243 Not recorded Extracellular Adherence Protein × 1 (Q99QS1) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;0.1M BisTris (pH 5.5), 0.2M Magnesium Chloride, 25% (w/v) PEG-3350 Resolution 1.95 Å R-free 0.261

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.

15 other PDB entries and 34 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CATG_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–223; UniProt 21–243 Author chain C; PDBConstruct 1–223; UniProt 21–243 Author chain E; PDBConstruct 1–223; UniProt 21–243 Author chain G; PDBConstruct 1–223; UniProt 21–243

Extracellular Adherence Protein

Staphylococcus aureus subsp. aureus Mu50

UniProt Q99QS1

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 B; UniProt 49–145 Not recorded Cathepsin G, C-terminal truncated form × 1 (P08311) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;0.1M BisTris (pH 5.5), 0.2M Magnesium Chloride, 25% (w/v) PEG-3350 Resolution 1.95 Å R-free 0.261
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 49–145 Not recorded Cathepsin G, C-terminal truncated form × 1 (P08311) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;0.1M BisTris (pH 5.5), 0.2M Magnesium Chloride, 25% (w/v) PEG-3350 Resolution 1.95 Å R-free 0.261
3 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain F; UniProt 49–145 Not recorded Cathepsin G, C-terminal truncated form × 1 (P08311) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;0.1M BisTris (pH 5.5), 0.2M Magnesium Chloride, 25% (w/v) PEG-3350 Resolution 1.95 Å R-free 0.261
4 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain H; UniProt 49–145 Not recorded Cathepsin G, C-terminal truncated form × 1 (P08311) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;0.1M BisTris (pH 5.5), 0.2M Magnesium Chloride, 25% (w/v) PEG-3350 Resolution 1.95 Å R-free 0.261

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.

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

View Construct and Data Evidence
UniProt name MAP_STAAM
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 4–100; UniProt 49–145 Author chain D; PDBConstruct 4–100; UniProt 49–145 Author chain F; PDBConstruct 4–100; UniProt 49–145 Author chain H; PDBConstruct 4–100; UniProt 49–145

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 8d4s

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8d4s
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8d4s
Deposition date deposition_date2022-06-02
Structure title titleCrystal Structure of Cathepsin G Inhibited by Eap1 from S. aureus
Keywords keywordsProtease Inhibitor, Immune Evasion, Neutrophil, S. aureus, PROTEIN BINDING; PROTEIN BINDING
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier43.32
Radius of gyration Rg (electron density) rg_electron43.11
Forward intensity I(0) i0338072000.00
Molecular weight molecular_weight144640.0 kDa
Excluded volume excluded_volume179240 ų
Envelope volume envelope_volume258980 ų
Hydration-shell volume shell_volume50602 ų
Envelope diameter envelope_diameter140.1
Shell Rg shell_rg47.77
Envelope Rg envelope_rg41.71
Shape Rg shape_rg43.09
Total Rg total_rg43.39
Total atoms total_atoms10164
Residues n_residues1268
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 dmax139.2
Rg (real space) rg_real43.24
Rg uncertainty (real space) rg_real_error1.13
I(0) (real space) i0_real3.3810e+08
I(0) uncertainty (real space) i0_real_error5.8770e+06
Rg (reciprocal space) rg_reciprocal43.32
I(0) (reciprocal space) i0_reciprocal338100000.0000
Solution quality estimate total_estimate0.8680
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary61.9
Skewness Skewness skewness0.108
Kurtosis Kurtosis kurtosis-0.662
Angular range angular_range— – 0.1800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha28870000.0000
Real-space data points n_real_points37
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.857; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.972; Smooth: 0.736

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)