7y0e

Crystal structure of TMPRSS2 in complex with Camostat

Method: X-RAY DIFFRACTION Dmax: 106.0 Å Quality: GOOD

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

Transmembrane protease serine 2 catalytic chain

Homo sapiens

UniProt O15393

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 109–254 Chain C; UniProt 256–492 Mutation:Residues 250-255 SSRQSR were replaced with DDDDK. NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 CA CALCIUM ION × 1 GBS 4-carbamimidamidobenzoic acid × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;0.1M acetic acid/sodium acetate, pH 5.0, 16% w/v PEG 8000 Resolution 2.39 Å R-free 0.239
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 109–254 Chain D; UniProt 256–492 Mutation:Residues 250-255 SSRQSR were replaced with DDDDK. NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 CA CALCIUM ION × 1 GBS 4-carbamimidamidobenzoic acid × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;0.1M acetic acid/sodium acetate, pH 5.0, 16% w/v PEG 8000 Resolution 2.39 Å R-free 0.239

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.

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

View Construct and Data Evidence
UniProt name TMPS2_HUMAN
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–146; UniProt 109–254 Author chain B; PDBConstruct 1–146; UniProt 109–254 Author chain C; PDBConstruct 1–237; UniProt 256–492 Author chain D; PDBConstruct 1–237; UniProt 256–492

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 7y0e

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7y0e
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7y0e
Deposition date deposition_date2022-06-04
Structure title titleCrystal structure of TMPRSS2 in complex with Camostat
Keywords keywordsInhibitor, Complex, Host, Antiviral, ANTIVIRAL PROTEIN, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.37
Radius of gyration Rg (electron density) rg_electron31.40
Forward intensity I(0) i0109254000.00
Molecular weight molecular_weight80372.0 kDa
Excluded volume excluded_volume99191 ų
Envelope volume envelope_volume125150 ų
Hydration-shell volume shell_volume33972 ų
Envelope diameter envelope_diameter112.8
Shell Rg shell_rg37.29
Envelope Rg envelope_rg31.54
Shape Rg shape_rg31.36
Total Rg total_rg32.01
Total atoms total_atoms5636
Residues n_residues740
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 dmax106.0
Rg (real space) rg_real32.50
Rg uncertainty (real space) rg_real_error0.77
I(0) (real space) i0_real1.0930e+08
I(0) uncertainty (real space) i0_real_error1.8780e+06
Rg (reciprocal space) rg_reciprocal32.45
I(0) (reciprocal space) i0_reciprocal109200000.0000
Solution quality estimate total_estimate0.8845
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary103.8
Skewness Skewness skewness0.366
Kurtosis Kurtosis kurtosis-0.529
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha15300000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.911; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.927; Smooth: 0.836

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)