8d4v

Crystal Structure of Cathepsin G Inhibited by Eap2 from S. aureus

Method: X-RAY DIFFRACTION Dmax: 116.0 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) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;0.1M BisTris (pH 6.5), 0.2M Ammonium Sulfate, 25%(w/v) PEG-3350 Resolution 1.85 Å R-free 0.251
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) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;0.1M BisTris (pH 6.5), 0.2M Ammonium Sulfate, 25%(w/v) PEG-3350 Resolution 1.85 Å R-free 0.251

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 36 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

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 158–254 Not recorded Cathepsin G, C-terminal truncated form × 1 (P08311) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;0.1M BisTris (pH 6.5), 0.2M Ammonium Sulfate, 25%(w/v) PEG-3350 Resolution 1.85 Å R-free 0.251
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 158–254 Not recorded Cathepsin G, C-terminal truncated form × 1 (P08311) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;0.1M BisTris (pH 6.5), 0.2M Ammonium Sulfate, 25%(w/v) PEG-3350 Resolution 1.85 Å R-free 0.251

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 35 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 158–254 Author chain D; PDBConstruct 4–100; UniProt 158–254

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 8d4v

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8d4v
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8d4v
Deposition date deposition_date2022-06-02
Structure title titleCrystal Structure of Cathepsin G Inhibited by Eap2 from S. aureus
Keywords keywordsProtease Inhibitor, Immune Evasion, Neutrophil, S. aureus, PROTEIN BINDING, HYDROLASE-INHIBITOR, PROTEIN BINDING complex; HYDROLASE/INHIBITOR,PROTEIN BINDING
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier31.79
Radius of gyration Rg (electron density) rg_electron32.11
Forward intensity I(0) i091076200.00
Molecular weight molecular_weight72480.0 kDa
Excluded volume excluded_volume89731 ų
Envelope volume envelope_volume115320 ų
Hydration-shell volume shell_volume31840 ų
Envelope diameter envelope_diameter125.0
Shell Rg shell_rg36.23
Envelope Rg envelope_rg32.80
Shape Rg shape_rg32.10
Total Rg total_rg32.46
Total atoms total_atoms5088
Residues n_residues641
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 dmax116.0
Rg (real space) rg_real32.19
Rg uncertainty (real space) rg_real_error1.17
I(0) (real space) i0_real9.1080e+07
I(0) uncertainty (real space) i0_real_error1.4610e+06
Rg (reciprocal space) rg_reciprocal32.02
I(0) (reciprocal space) i0_reciprocal91060000.0000
Solution quality estimate total_estimate0.7886
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.8
Skewness Skewness skewness0.618
Kurtosis Kurtosis kurtosis-0.123
Angular range angular_range— – 0.2500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha34130000.0000
Real-space data points n_real_points51
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.560; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.672; Smooth: 0.896

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)