9k3t

Cryo-EM structure of TMPRSS2 in complex with Fab fragments of 752 mAb and 2228 mAb

Method: ELECTRON MICROSCOPY Dmax: 125.1 Å Quality: GOOD

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

Transmembrane protease serine 2

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 heterocomplex Heteromer Protein × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain A; UniProt 109–492 Mutation:250SSRQSR255 replaced with DDDDDK Fab 752 light chain × 1 Fab 752 heavy chain × 1 Fab 2228 light chain × 1 Fab 2228 heavy chain × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.15 Å

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 42 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TMPS2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–385; UniProt 109–492

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 9k3t

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9k3t
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9k3t
Deposition date deposition_date2024-10-20
Structure title titleCryo-EM structure of TMPRSS2 in complex with Fab fragments of 752 mAb and 2228 mAb
Keywords keywordsHYDROLASE, IMMUNE SYSTEM, MEMBRANE PROTEIN; MEMBRANE PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier37.33
Radius of gyration Rg (electron density) rg_electron37.05
Forward intensity I(0) i0174251000.00
Molecular weight molecular_weight105580.0 kDa
Excluded volume excluded_volume131570 ų
Envelope volume envelope_volume176720 ų
Hydration-shell volume shell_volume40665 ų
Envelope diameter envelope_diameter124.3
Shell Rg shell_rg41.77
Envelope Rg envelope_rg37.08
Shape Rg shape_rg37.01
Total Rg total_rg37.52
Total atoms total_atoms14609
Residues n_residues967
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 dmax125.1
Rg (real space) rg_real37.48
Rg uncertainty (real space) rg_real_error0.91
I(0) (real space) i0_real1.7430e+08
I(0) uncertainty (real space) i0_real_error2.9010e+06
Rg (reciprocal space) rg_reciprocal37.39
I(0) (reciprocal space) i0_reciprocal174200000.0000
Solution quality estimate total_estimate0.8828
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary35.7
Skewness Skewness skewness0.337
Kurtosis Kurtosis kurtosis-0.632
Angular range angular_range— – 0.2100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha17720000.0000
Real-space data points n_real_points43
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.877; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.929; Smooth: 0.913

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)