7cbk

Structure of Human Neutrophil Elastase Ecotin complex

Method: X-RAY DIFFRACTION Dmax: 110.6 Å Quality: GOOD

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

Ecotin

Escherichia coli K-12

UniProt P23827

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 × 4 其他Polymer 3 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 1–162 Chain C; UniProt 1–162 Not recorded Neutrophil elastase × 2 (P08246) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose × 3 GOL GLYCEROL × 1 SO4 SULFATE ION × 2 MG MAGNESIUM ION × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;298 K;0.2 M Ammonium sulfate, 0.1 M BIS-TRIS pH 5.5 and 25% w/v Polyethylene glycol 3,350 Resolution 2.70 Å R-free 0.266

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.

21 other PDB entries and 26 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ECOT_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–162; UniProt 1–162 Author chain C; PDBConstruct 1–162; UniProt 1–162

Neutrophil elastase

OrganismNot specified

UniProt P08246

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 × 4 其他Polymer 3 PDB declaration: tetrameric(4) Consistent with protein copy count Chain B; UniProt 1–267 Chain D; UniProt 1–267 Not recorded Ecotin × 2 (P23827) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose × 3 GOL GLYCEROL × 1 SO4 SULFATE ION × 2 MG MAGNESIUM ION × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;298 K;0.2 M Ammonium sulfate, 0.1 M BIS-TRIS pH 5.5 and 25% w/v Polyethylene glycol 3,350 Resolution 2.70 Å R-free 0.266

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.

37 other PDB entries and 70 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ELNE_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–267; UniProt 1–267 Author chain D; PDBConstruct 1–267; UniProt 1–267

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 7cbk

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7cbk
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7cbk
Deposition date deposition_date2020-06-12
Structure title titleStructure of Human Neutrophil Elastase Ecotin complex
Keywords keywordsProtease-inhibitor complex, LYASE; LYASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.22
Radius of gyration Rg (electron density) rg_electron31.74
Forward intensity I(0) i098359200.00
Molecular weight molecular_weight78082.0 kDa
Excluded volume excluded_volume97654 ų
Envelope volume envelope_volume126550 ų
Hydration-shell volume shell_volume34801 ų
Envelope diameter envelope_diameter114.6
Shell Rg shell_rg37.04
Envelope Rg envelope_rg31.24
Shape Rg shape_rg31.71
Total Rg total_rg32.29
Total atoms total_atoms5477
Residues n_residues684
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 dmax110.6
Rg (real space) rg_real32.47
Rg uncertainty (real space) rg_real_error1.02
I(0) (real space) i0_real9.8360e+07
I(0) uncertainty (real space) i0_real_error1.5890e+06
Rg (reciprocal space) rg_reciprocal32.37
I(0) (reciprocal space) i0_reciprocal98350000.0000
Solution quality estimate total_estimate0.8485
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary29.4
Skewness Skewness skewness0.492
Kurtosis Kurtosis kurtosis-0.362
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha43920000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.782; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.836; Smooth: 0.844

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

8. Citations (1)

9. Files and Curves (10)