7a0d

The Crystal Structure of Bovine Thrombin in complex with Hirudin (C16U/C28U) at 1.6 Angstroms Resolution

Method: X-RAY DIFFRACTION Dmax: 67.0 Å Quality: REASONABLE

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

Prothrombin

OrganismNot specified

UniProt P00735

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 HHH; UniProt 367–625 Chain LLL; UniProt 318–366 Not recorded Hirudin variant-1 × 1 (P01050) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.7;297 K;38% PEG 4000, 0.1 M sodium phosphate (pH= 4.7), 0.2 M NaCl Resolution 1.60 Å R-free 0.215

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.

30 other PDB entries and 55 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name THRB_BOVIN
Isoform
PDB entities 1, 3
Chains and sequence ranges Author chain HHH; PDBConstruct 1–259; UniProt 367–625 Author chain LLL; PDBConstruct 1–49; UniProt 318–366

Hirudin variant-1

OrganismNot specified

UniProt P01050

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 III; UniProt 1–65 Mutation:C16U/C28U Prothrombin × 1 (P00735) Prothrombin × 1 (P00735) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.7;297 K;38% PEG 4000, 0.1 M sodium phosphate (pH= 4.7), 0.2 M NaCl Resolution 1.60 Å R-free 0.215

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.

48 other PDB entries and 48 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name HIRV1_HIRME
Isoform
PDB entities 2
Chains and sequence ranges Author chain III; PDBConstruct 1–65; UniProt 1–65

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 7a0d

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7a0d
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7a0d
Deposition date deposition_date2020-08-07
Structure title titleThe Crystal Structure of Bovine Thrombin in complex with Hirudin (C16U/C28U) at 1.6 Angstroms Resolution
Keywords keywordsHydrolase, Inhibitor, Hirudin, Thrombin, Selenocysteine, Derivative; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier20.95
Radius of gyration Rg (electron density) rg_electron19.73
Forward intensity I(0) i028718200.00
Molecular weight molecular_weight40391.0 kDa
Excluded volume excluded_volume50214 ų
Envelope volume envelope_volume58783 ų
Hydration-shell volume shell_volume24068 ų
Envelope diameter envelope_diameter69.0
Shell Rg shell_rg27.20
Envelope Rg envelope_rg20.16
Shape Rg shape_rg19.69
Total Rg total_rg20.80
Total atoms total_atoms2830
Residues n_residues356
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 dmax67.0
Rg (real space) rg_real20.83
Rg uncertainty (real space) rg_real_error0.35
I(0) (real space) i0_real2.8720e+07
I(0) uncertainty (real space) i0_real_error3.8740e+05
Rg (reciprocal space) rg_reciprocal20.85
I(0) (reciprocal space) i0_reciprocal28720000.0000
Solution quality estimate total_estimate0.6960
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.2
Skewness Skewness skewness0.202
Kurtosis Kurtosis kurtosis-0.314
Angular range angular_range— – 0.3800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6716000.0000
Real-space data points n_real_points70
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.856; Stabil: 1.000; Sysdev: 0.177; Positv: 1.000; Valcen: 0.991; Smooth: 0.953

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)