3km9

Structure of complement C5 in complex with the C-terminal beta-grasp domain of SSL7

Method: X-RAY DIFFRACTION Dmax: 168.7 Å Quality: GOOD

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

Complement C5

OrganismNot specified

UniProt P01031

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Heteromer Protein × 2 其他Polymer 1 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–1676 Not recorded Staphylococcal enterotoxin-like toxin × 1 (A6QE84) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 CD CADMIUM ION × 3 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 6.2;277 K;Reservoir contains 50mM MgAc2, 50mM MES pH 6.2. Mixed 1:1 with concentrated protein, VAPOR DIFFUSION, temperature 277K Resolution 4.20 Å R-free 0.297
2 Other combination Heteromer Protein × 2 其他Polymer 1 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 1–1676 Not recorded Staphylococcal enterotoxin-like toxin × 1 (A6QE84) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 CD CADMIUM ION × 2 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 6.2;277 K;Reservoir contains 50mM MgAc2, 50mM MES pH 6.2. Mixed 1:1 with concentrated protein, VAPOR DIFFUSION, temperature 277K Resolution 4.20 Å R-free 0.297

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.

41 other PDB entries and 62 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CO5_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–1676; UniProt 1–1676 Author chain B; PDBConstruct 1–1676; UniProt 1–1676

Staphylococcal enterotoxin-like toxin

Staphylococcus aureus subsp. aureus

UniProt A6QE84

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Heteromer Protein × 2 其他Polymer 1 PDB declaration: dimeric(2) Consistent with protein copy count Chain X; UniProt 129–231 Fragment:C-terminal beta-grasp domain, residues 129-231 Complement C5 × 1 (P01031) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 CD CADMIUM ION × 3 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 6.2;277 K;Reservoir contains 50mM MgAc2, 50mM MES pH 6.2. Mixed 1:1 with concentrated protein, VAPOR DIFFUSION, temperature 277K Resolution 4.20 Å R-free 0.297
2 Other combination Heteromer Protein × 2 其他Polymer 1 PDB declaration: dimeric(2) Consistent with protein copy count Chain Y; UniProt 129–231 Fragment:C-terminal beta-grasp domain, residues 129-231 Complement C5 × 1 (P01031) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 CD CADMIUM ION × 2 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 6.2;277 K;Reservoir contains 50mM MgAc2, 50mM MES pH 6.2. Mixed 1:1 with concentrated protein, VAPOR DIFFUSION, temperature 277K Resolution 4.20 Å R-free 0.297

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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name A6QE84_STAAE
Isoform
PDB entities 2
Chains and sequence ranges Author chain X; PDBConstruct 1–103; UniProt 129–231 Author chain Y; PDBConstruct 1–103; UniProt 129–231

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 3km9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3km9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3km9
Deposition date deposition_date2009-11-10
Structure title titleStructure of complement C5 in complex with the C-terminal beta-grasp domain of SSL7
Keywords keywords;OB-fold, beta-grasp domain, FN3 domain, Cleavage on pair of basic residues, Complement alternate pathway, Complement pathway, Cytolysis, Disulfide bond, Glycoprotein, Immune response, Inflammatory response, Innate immunity, Membrane attack complex, Secreted, IMMUNE SYSTEM ;; IMMUNE SYSTEM
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier58.19
Radius of gyration Rg (electron density) rg_electron58.17
Forward intensity I(0) i01668960000.00
Molecular weight molecular_weight352360.0 kDa
Excluded volume excluded_volume444700 ų
Envelope volume envelope_volume657440 ų
Hydration-shell volume shell_volume95648 ų
Envelope diameter envelope_diameter180.0
Shell Rg shell_rg59.03
Envelope Rg envelope_rg56.03
Shape Rg shape_rg58.20
Total Rg total_rg58.08
Total atoms total_atoms24809
Residues n_residues3122
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 dmax168.7
Rg (real space) rg_real58.14
Rg uncertainty (real space) rg_real_error1.26
I(0) (real space) i0_real1.6690e+09
I(0) uncertainty (real space) i0_real_error3.0210e+07
Rg (reciprocal space) rg_reciprocal58.19
I(0) (reciprocal space) i0_reciprocal1669000000.0000
Solution quality estimate total_estimate0.8464
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary75.0
Skewness Skewness skewness0.192
Kurtosis Kurtosis kurtosis-0.690
Angular range angular_range— – 0.1350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha151500000.0000
Real-space data points n_real_points28
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 1.000; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)