9xyl

Human prolyl endopeptidase (PREP) - complex with S17092

Method: X-RAY DIFFRACTION Dmax: 235.2 Å Quality: REASONABLE

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

Prolyl endopeptidase

Homo sapiens

UniProt P48147

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–710 Not recorded A1CRK {(2S,3aS,7aS)-1-[(1R,2R)-2-phenylcyclopropane-1-carbonyl]octahydro-1H-indol-2-yl}(1,3-thiazolidin-3-yl)methanone × 1 GOL GLYCEROL × 4 SCN THIOCYANATE ION × 1 PEG DI(HYDROXYETHYL)ETHER × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;277 K;25-30% PEG 3350, 200 mM KSCN and 100 mM bis-tris propane pH 7.5 Resolution 1.81 Å R-free 0.249
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 1–710 Not recorded A1CRK {(2S,3aS,7aS)-1-[(1R,2R)-2-phenylcyclopropane-1-carbonyl]octahydro-1H-indol-2-yl}(1,3-thiazolidin-3-yl)methanone × 1 GOL GLYCEROL × 3 SCN THIOCYANATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;277 K;25-30% PEG 3350, 200 mM KSCN and 100 mM bis-tris propane pH 7.5 Resolution 1.81 Å R-free 0.249
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 1–710 Not recorded A1CRK {(2S,3aS,7aS)-1-[(1R,2R)-2-phenylcyclopropane-1-carbonyl]octahydro-1H-indol-2-yl}(1,3-thiazolidin-3-yl)methanone × 1 GOL GLYCEROL × 2 SCN THIOCYANATE ION × 2 B3P 2-[3-(2-HYDROXY-1,1-DIHYDROXYMETHYL-ETHYLAMINO)-PROPYLAMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;277 K;25-30% PEG 3350, 200 mM KSCN and 100 mM bis-tris propane pH 7.5 Resolution 1.81 Å R-free 0.249
4 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain D; UniProt 1–710 Not recorded A1CRK {(2S,3aS,7aS)-1-[(1R,2R)-2-phenylcyclopropane-1-carbonyl]octahydro-1H-indol-2-yl}(1,3-thiazolidin-3-yl)methanone × 1 GOL GLYCEROL × 1 SCN THIOCYANATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;277 K;25-30% PEG 3350, 200 mM KSCN and 100 mM bis-tris propane pH 7.5 Resolution 1.81 Å R-free 0.249
5 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain E; UniProt 1–710 Not recorded A1CRK {(2S,3aS,7aS)-1-[(1R,2R)-2-phenylcyclopropane-1-carbonyl]octahydro-1H-indol-2-yl}(1,3-thiazolidin-3-yl)methanone × 1 GOL GLYCEROL × 2 SCN THIOCYANATE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;277 K;25-30% PEG 3350, 200 mM KSCN and 100 mM bis-tris propane pH 7.5 Resolution 1.81 Å R-free 0.249
6 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain F; UniProt 1–710 Not recorded A1CRK {(2S,3aS,7aS)-1-[(1R,2R)-2-phenylcyclopropane-1-carbonyl]octahydro-1H-indol-2-yl}(1,3-thiazolidin-3-yl)methanone × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;277 K;25-30% PEG 3350, 200 mM KSCN and 100 mM bis-tris propane pH 7.5 Resolution 1.81 Å R-free 0.249

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 43 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PPCE_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–711; UniProt 1–710 Author chain B; PDBConstruct 2–711; UniProt 1–710 Author chain C; PDBConstruct 2–711; UniProt 1–710 Author chain D; PDBConstruct 2–711; UniProt 1–710 Author chain E; PDBConstruct 2–711; UniProt 1–710 Author chain F; PDBConstruct 2–711; UniProt 1–710

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 9xyl

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9xyl
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9xyl
Deposition date deposition_date2025-08-26
Structure title titleHuman prolyl endopeptidase (PREP) - complex with S17092
Keywords keywordsinhibitor-bound, peptide cleavage, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier72.91
Radius of gyration Rg (electron density) rg_electron73.73
Forward intensity I(0) i03168360000.00
Molecular weight molecular_weight486410.0 kDa
Excluded volume excluded_volume612120 ų
Envelope volume envelope_volume881170 ų
Hydration-shell volume shell_volume111240 ų
Envelope diameter envelope_diameter270.5
Shell Rg shell_rg61.23
Envelope Rg envelope_rg72.82
Shape Rg shape_rg73.69
Total Rg total_rg73.66
Total atoms total_atoms67703
Residues n_residues4242
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 dmax235.2
Rg (real space) rg_real72.53
Rg uncertainty (real space) rg_real_error1.75
I(0) (real space) i0_real3.1500e+09
I(0) uncertainty (real space) i0_real_error6.3730e+07
Rg (reciprocal space) rg_reciprocal70.26
I(0) (reciprocal space) i0_reciprocal3148000000.0000
Solution quality estimate total_estimate0.6497
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary67.2
Skewness Skewness skewness0.640
Kurtosis Kurtosis kurtosis-0.048
Angular range angular_range— – 0.1050 −1
Current regularization parameter α current_alpha0.0707
Highest regularization parameter α highest_alpha100500000.0000
Real-space data points n_real_points22
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.848; Stabil: 0.996; Sysdev: 0.020; Positv: 1.000; Valcen: 0.991; Smooth: 0.837

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)