2pux

Crystal structure of murine thrombin in complex with the extracellular fragment of murine PAR3

Method: X-RAY DIFFRACTION Dmax: 59.9 Å Quality: EXCELLENT

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 Not recorded Proteinase-activated receptor 3 × 1 (O08675) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;295 K;20% PEG 10000, 100 mM HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 2.00 Å R-free 0.225

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 12 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 3

OrganismNot specified

UniProt O08675

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 44–56 Not recorded Thrombin light chain × 1 (P19221) Thrombin heavy chain × 1 (P19221) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;295 K;20% PEG 10000, 100 mM HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 2.00 Å R-free 0.225

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 PAR3_MOUSE
Isoform
PDB entities 3
Chains and sequence ranges Author chain C; PDBConstruct 1–13; UniProt 44–56

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 2pux

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2pux
Deposition date deposition_date2007-05-09
Structure title titleCrystal structure of murine thrombin in complex with the extracellular fragment of murine PAR3
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_guinier19.82
Radius of gyration Rg (electron density) rg_electron18.55
Forward intensity I(0) i022245300.00
Molecular weight molecular_weight36544.0 kDa
Excluded volume excluded_volume45975 ų
Envelope volume envelope_volume51965 ų
Hydration-shell volume shell_volume22418 ų
Envelope diameter envelope_diameter61.6
Shell Rg shell_rg25.84
Envelope Rg envelope_rg18.87
Shape Rg shape_rg18.54
Total Rg total_rg19.59
Total atoms total_atoms2577
Residues n_residues257
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 dmax59.9
Rg (real space) rg_real19.63
Rg uncertainty (real space) rg_real_error0.23
I(0) (real space) i0_real2.2250e+07
I(0) uncertainty (real space) i0_real_error2.6480e+05
Rg (reciprocal space) rg_reciprocal19.66
I(0) (reciprocal space) i0_reciprocal22250000.0000
Solution quality estimate total_estimate0.9003
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.2
Skewness Skewness skewness0.055
Kurtosis Kurtosis kurtosis-0.491
Angular range angular_range— – 0.4000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7168000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.910; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.977; Smooth: 0.992

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 3 domains

CATH v4.4 (3 domains)

Domain ID domain_id2puxA00
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_id2puxB01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases
Domain ID domain_id2puxB02
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)