1mkx

THE CO-CRYSTAL STRUCTURE OF UNLIGANDED BOVINE ALPHA-THROMBIN AND PRETHROMBIN-2: MOVEMENT OF THE YPPW SEGMENT AND ACTIVE SITE RESIDUES UPON LIGAND BINDING

Method: X-RAY DIFFRACTION Dmax: 93.2 Å Quality: GOOD

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

ALPHA-THROMBIN

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 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain H; UniProt 367–625 Chain L; UniProt 318–366 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.8;38% AMMONIUM SULFATE, 0.25M AMMONIUM PHOSPHATE, PH 5.8, 1% POLYETHYLENE GLYCOL 4000 (DROP ONLY). Resolution 2.20 Å R-free 0.255
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain K; UniProt 318–625 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.8;38% AMMONIUM SULFATE, 0.25M AMMONIUM PHOSPHATE, PH 5.8, 1% POLYETHYLENE GLYCOL 4000 (DROP ONLY). Resolution 2.20 Å R-free 0.255
3 Protein homooligomer Homooligomer Protein × 6 PDB declaration: hexameric(6) Consistent with protein copy count Chain H; UniProt 367–625 Chain K; UniProt 318–625 Chain L; UniProt 318–366 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.8;38% AMMONIUM SULFATE, 0.25M AMMONIUM PHOSPHATE, PH 5.8, 1% POLYETHYLENE GLYCOL 4000 (DROP ONLY). Resolution 2.20 Å R-free 0.255
4 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain K; UniProt 318–625 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.8;38% AMMONIUM SULFATE, 0.25M AMMONIUM PHOSPHATE, PH 5.8, 1% POLYETHYLENE GLYCOL 4000 (DROP ONLY). Resolution 2.20 Å R-free 0.255
5 Protein homooligomer Homooligomer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain H; UniProt 367–625 Chain K; UniProt 318–625 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.8;38% AMMONIUM SULFATE, 0.25M AMMONIUM PHOSPHATE, PH 5.8, 1% POLYETHYLENE GLYCOL 4000 (DROP ONLY). Resolution 2.20 Å R-free 0.255
6 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain L; UniProt 318–366 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.8;38% AMMONIUM SULFATE, 0.25M AMMONIUM PHOSPHATE, PH 5.8, 1% POLYETHYLENE GLYCOL 4000 (DROP ONLY). Resolution 2.20 Å R-free 0.255

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 50 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name THRB_BOVIN
Isoform
PDB entities 1, 2, 3
Chains and sequence ranges Author chain L; PDBConstruct 1–49; UniProt 318–366 Author chain H; PDBConstruct 1–259; UniProt 367–625 Author chain K; PDBConstruct 1–308; UniProt 318–625

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 1mkx

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1mkx
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1mkx
Deposition date deposition_date1997-03-13
Structure title titleTHE CO-CRYSTAL STRUCTURE OF UNLIGANDED BOVINE ALPHA-THROMBIN AND PRETHROMBIN-2: MOVEMENT OF THE YPPW SEGMENT AND ACTIVE SITE RESIDUES UPON LIGAND BINDING
Keywords keywords;COMPLEX (BLOOD COAGULATION-PROENZYME), THROMBIN, PRETHROMBIN-2, PLASMA, SERINE PROTEASE, COMPLEX (BLOOD COAGULATION-PROENZYME) complex ;; COMPLEX (BLOOD COAGULATION/PROENZYME)
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.73
Radius of gyration Rg (electron density) rg_electron28.45
Forward intensity I(0) i069230300.00
Molecular weight molecular_weight65788.0 kDa
Excluded volume excluded_volume82635 ų
Envelope volume envelope_volume101890 ų
Hydration-shell volume shell_volume30804 ų
Envelope diameter envelope_diameter99.5
Shell Rg shell_rg34.81
Envelope Rg envelope_rg28.24
Shape Rg shape_rg28.44
Total Rg total_rg29.15
Total atoms total_atoms4633
Residues n_residues483
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 dmax93.2
Rg (real space) rg_real28.85
Rg uncertainty (real space) rg_real_error0.69
I(0) (real space) i0_real6.9230e+07
I(0) uncertainty (real space) i0_real_error1.1190e+06
Rg (reciprocal space) rg_reciprocal28.80
I(0) (reciprocal space) i0_reciprocal69230000.0000
Solution quality estimate total_estimate0.8631
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.1
Skewness Skewness skewness0.444
Kurtosis Kurtosis kurtosis-0.505
Angular range angular_range— – 0.2750 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha56560000.0000
Real-space data points n_real_points56
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.798; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.888; Smooth: 0.933

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1mkx.1
Class classb — All beta proteins
Fold Fold foldb.47 — Trypsin-like serine proteases
Superfamily Superfamily superfamilyb.47.1 — Trypsin-like serine proteases
Family Family familyb.47.1.2 — Eukaryotic proteases
Domain ID domain_idd1mkxk_
Class classb — All beta proteins
Fold Fold foldb.47 — Trypsin-like serine proteases
Superfamily Superfamily superfamilyb.47.1 — Trypsin-like serine proteases
Family Family familyb.47.1.2 — Eukaryotic proteases

CATH v4.4 (4 domains)

Domain ID domain_id1mkxH01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases
Domain ID domain_id1mkxH02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases
Domain ID domain_id1mkxK01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases
Domain ID domain_id1mkxK02
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)