9q6k

Human prolyl endopeptidase (PREP) - complex with JP-2-1-7

Method: X-RAY DIFFRACTION Dmax: 165.6 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 A1CQZ 4-chloro-3-methyl-N-[2-oxo-2-(pyrrolidin-1-yl)ethyl]-1-(2-phenylethyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxamide × 1 B3P 2-[3-(2-HYDROXY-1,1-DIHYDROXYMETHYL-ETHYLAMINO)-PROPYLAMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL × 2 GOL GLYCEROL × 5 PEG DI(HYDROXYETHYL)ETHER × 1 SCN THIOCYANATE ION × 9 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 1.85 Å R-free 0.272
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 1–710 Not recorded A1CQZ 4-chloro-3-methyl-N-[2-oxo-2-(pyrrolidin-1-yl)ethyl]-1-(2-phenylethyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxamide × 1 GOL GLYCEROL × 4 SCN THIOCYANATE ION × 8 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 1.85 Å R-free 0.272
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 1–710 Not recorded A1CQZ 4-chloro-3-methyl-N-[2-oxo-2-(pyrrolidin-1-yl)ethyl]-1-(2-phenylethyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxamide × 1 GOL GLYCEROL × 3 SCN THIOCYANATE ION × 3 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 1.85 Å R-free 0.272

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 46 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

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 9q6k

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9q6k
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9q6k
Deposition date deposition_date2025-08-22
Structure title titleHuman prolyl endopeptidase (PREP) - complex with JP-2-1-7
Keywords keywordsinhibitor-bound, peptide cleavage, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR complex; HYDROLASE/HYDROLASE INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier51.39
Radius of gyration Rg (electron density) rg_electron51.86
Forward intensity I(0) i0843446000.00
Molecular weight molecular_weight245210.0 kDa
Excluded volume excluded_volume307950 ų
Envelope volume envelope_volume412920 ų
Hydration-shell volume shell_volume71842 ų
Envelope diameter envelope_diameter174.0
Shell Rg shell_rg48.97
Envelope Rg envelope_rg51.30
Shape Rg shape_rg51.86
Total Rg total_rg51.75
Total atoms total_atoms34055
Residues n_residues2121
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 dmax165.6
Rg (real space) rg_real51.83
Rg uncertainty (real space) rg_real_error1.80
I(0) (real space) i0_real8.4340e+08
I(0) uncertainty (real space) i0_real_error1.6250e+07
Rg (reciprocal space) rg_reciprocal51.00
I(0) (reciprocal space) i0_reciprocal842500000.0000
Solution quality estimate total_estimate0.5469
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary42.7
Skewness Skewness skewness0.579
Kurtosis Kurtosis kurtosis-0.432
Angular range angular_range— – 0.1550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha249100000.0000
Real-space data points n_real_points32
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.744; Stabil: 0.995; Sysdev: 0.029; Positv: 1.000; Valcen: 0.790; Smooth: 0.013

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)