8s0m

Crystal structure of the HKU1 receptor binding domain in complex with TMPRSS2 and the nanobody A01

Method: X-RAY DIFFRACTION Dmax: 164.0 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 Other combination Heteromer Protein × 3 其他Polymer 1 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 107–492 Not recorded Nanobody A01 × 1 Spike protein S1 × 1 (Q0ZME7) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 3 PO4 PHOSPHATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;277 K;0.35 M NaH2PO4, 0.65 M K2HPO4 Resolution 3.55 Å R-free 0.221
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain E; UniProt 107–492 Not recorded Nanobody A01 × 1 Spike protein S1 × 1 (Q0ZME7) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 PO4 PHOSPHATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;277 K;0.35 M NaH2PO4, 0.65 M K2HPO4 Resolution 3.55 Å R-free 0.221

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
Chains and sequence ranges Author chain B; PDBConstruct 1–386; UniProt 107–492 Author chain E; PDBConstruct 1–386; UniProt 107–492

Spike protein S1

Human coronavirus HKU1 (isolate N5)

UniProt Q0ZME7

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 × 3 其他Polymer 1 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 307–672 Not recorded Transmembrane protease serine 2 × 1 (O15393) Nanobody A01 × 1 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 3 PO4 PHOSPHATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;277 K;0.35 M NaH2PO4, 0.65 M K2HPO4 Resolution 3.55 Å R-free 0.221
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain D; UniProt 307–672 Not recorded Transmembrane protease serine 2 × 1 (O15393) Nanobody A01 × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 PO4 PHOSPHATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;277 K;0.35 M NaH2PO4, 0.65 M K2HPO4 Resolution 3.55 Å R-free 0.221

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 15 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SPIKE_CVHN5
Isoform
PDB entities 3
Chains and sequence ranges Author chain A; PDBConstruct 1–366; UniProt 307–672 Author chain D; PDBConstruct 1–366; UniProt 307–672

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 8s0m

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8s0m
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8s0m
Deposition date deposition_date2024-02-14
Structure title titleCrystal structure of the HKU1 receptor binding domain in complex with TMPRSS2 and the nanobody A01
Keywords keywordscoronavirus receptor, VIRAL PROTEIN, PROTEASE, NANOBODY, VIRAL PROTEIN-RECEPTOR complex; VIRAL PROTEIN/RECEPTOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier48.93
Radius of gyration Rg (electron density) rg_electron49.28
Forward intensity I(0) i0506018000.00
Molecular weight molecular_weight180480.0 kDa
Excluded volume excluded_volume223140 ų
Envelope volume envelope_volume328960 ų
Hydration-shell volume shell_volume57839 ų
Envelope diameter envelope_diameter171.9
Shell Rg shell_rg50.50
Envelope Rg envelope_rg48.53
Shape Rg shape_rg49.29
Total Rg total_rg49.27
Total atoms total_atoms12661
Residues n_residues1626
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 dmax164.0
Rg (real space) rg_real48.94
Rg uncertainty (real space) rg_real_error1.78
I(0) (real space) i0_real5.0600e+08
I(0) uncertainty (real space) i0_real_error9.3800e+06
Rg (reciprocal space) rg_reciprocal48.93
I(0) (reciprocal space) i0_reciprocal506000000.0000
Solution quality estimate total_estimate0.8941
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary61.5
Skewness Skewness skewness0.187
Kurtosis Kurtosis kurtosis-0.616
Angular range angular_range— – 0.1600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha14600000.0000
Real-space data points n_real_points33
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.925; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.979; Smooth: 0.867

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (2)

9. Files and Curves (10)