2pv9

Crystal structure of murine thrombin in complex with the extracellular fragment of murine PAR4

Method: X-RAY DIFFRACTION Dmax: 66.4 Å Quality: REASONABLE

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

Thrombin light chain

Mus musculus

UniProt P19221

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 317–360 Chain B; UniProt 361–618 Mutation:S195A Proteinase-activated receptor 4 × 1 (O88634) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.9;295 K;20% PEG 3350, 200 mM MgSO4, pH 5.9, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 3.50 Å R-free 0.319
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 317–360 Chain B; UniProt 361–618 Mutation:S195A Proteinase-activated receptor 4 × 1 (O88634) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.9;295 K;20% PEG 3350, 200 mM MgSO4, pH 5.9, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 3.50 Å R-free 0.319

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.

6 other PDB entries and 11 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name THRB_MOUSE
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–44; UniProt 317–360 Author chain B; PDBConstruct 1–258; UniProt 361–618

Proteinase-activated receptor 4

OrganismNot specified

UniProt O88634

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 51–76 Not recorded Thrombin light chain × 1 (P19221) Thrombin heavy chain × 1 (P19221) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.9;295 K;20% PEG 3350, 200 mM MgSO4, pH 5.9, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 3.50 Å R-free 0.319
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 51–76 Not recorded Thrombin light chain × 1 (P19221) Thrombin heavy chain × 1 (P19221) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.9;295 K;20% PEG 3350, 200 mM MgSO4, pH 5.9, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 3.50 Å R-free 0.319

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 PAR4_MOUSE
Isoform
PDB entities 3
Chains and sequence ranges Author chain C; PDBConstruct 1–26; UniProt 51–76

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 2pv9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2pv9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2pv9
Deposition date deposition_date2007-05-09
Structure title titleCrystal structure of murine thrombin in complex with the extracellular fragment of murine PAR4
Keywords keywordsSerine protease, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier20.09
Radius of gyration Rg (electron density) rg_electron18.93
Forward intensity I(0) i024198300.00
Molecular weight molecular_weight38021.0 kDa
Excluded volume excluded_volume47770 ų
Envelope volume envelope_volume54722 ų
Hydration-shell volume shell_volume23062 ų
Envelope diameter envelope_diameter69.4
Shell Rg shell_rg26.52
Envelope Rg envelope_rg19.61
Shape Rg shape_rg18.91
Total Rg total_rg20.01
Total atoms total_atoms2679
Residues n_residues270
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 dmax66.4
Rg (real space) rg_real19.97
Rg uncertainty (real space) rg_real_error0.36
I(0) (real space) i0_real2.4200e+07
I(0) uncertainty (real space) i0_real_error2.7650e+05
Rg (reciprocal space) rg_reciprocal20.00
I(0) (reciprocal space) i0_reciprocal24200000.0000
Solution quality estimate total_estimate0.6528
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary25.6
Skewness Skewness skewness0.205
Kurtosis Kurtosis kurtosis-0.215
Angular range angular_range— – 0.3950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha11690000.0000
Real-space data points n_real_points71
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.758; Stabil: 1.000; Sysdev: 0.406; Positv: 1.000; Valcen: 0.991; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 3 domains

CATH v4.4 (3 domains)

Domain ID domain_id2pv9A00
Class class4 — Few Secondary Structures
Architecture architecture10 — Irregular
Topology topology140 — Epsilon-Thrombin; Chain L
Homologous superfamily homologous superfamily10 — Thrombin light chain domain
Domain ID domain_id2pv9B01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases
Domain ID domain_id2pv9B02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases

8. Citations (3)

9. Files and Curves (10)