9ct1

Complex between the porcine trypsin and M271 a Kunitz-STI from Solanum tuberosum

Method: X-RAY DIFFRACTION Dmax: 103.9 Å Quality: GOOD

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

Trypsin

OrganismNot specified

UniProt P00761

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–231 Not recorded KTI-A protein × 1 (A0A097H115) CA CALCIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:BATCH MODE;pH 4.6;293 K;0.085 M Sodium acetate trihydrate pH 4.6, 0.17 M Ammonium acetate, 25.5% w/v Polyethylene glycol 4,000, 15% v/v Glycerol Resolution 2.42 Å R-free 0.244
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 1–231 Not recorded KTI-A protein × 1 (A0A097H115) CA CALCIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:BATCH MODE;pH 4.6;293 K;0.085 M Sodium acetate trihydrate pH 4.6, 0.17 M Ammonium acetate, 25.5% w/v Polyethylene glycol 4,000, 15% v/v Glycerol Resolution 2.42 Å R-free 0.244

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.

44 other PDB entries and 53 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TRYP_PIG
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–231; UniProt 1–231 Author chain C; PDBConstruct 1–231; UniProt 1–231

KTI-A protein

Solanum tuberosum

UniProt A0A097H115

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 33–221 Not recorded Trypsin × 1 (P00761) CA CALCIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:BATCH MODE;pH 4.6;293 K;0.085 M Sodium acetate trihydrate pH 4.6, 0.17 M Ammonium acetate, 25.5% w/v Polyethylene glycol 4,000, 15% v/v Glycerol Resolution 2.42 Å R-free 0.244
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 33–221 Not recorded Trypsin × 1 (P00761) CA CALCIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:BATCH MODE;pH 4.6;293 K;0.085 M Sodium acetate trihydrate pH 4.6, 0.17 M Ammonium acetate, 25.5% w/v Polyethylene glycol 4,000, 15% v/v Glycerol Resolution 2.42 Å R-free 0.244

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.

1 other PDB entries and 1 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A097H115_SOLTU
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–189; UniProt 33–221 Author chain D; PDBConstruct 1–189; UniProt 33–221

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 9ct1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9ct1
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9ct1
Deposition date deposition_date2024-07-24
Structure title titleComplex between the porcine trypsin and M271 a Kunitz-STI from Solanum tuberosum
Keywords keywordsKunitz, Serine Proteases, Serine Proteinase Inhibitors, Soybean Trypsin Inhibitor, Trypsin Inhibitor, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier31.27
Radius of gyration Rg (electron density) rg_electron30.94
Forward intensity I(0) i0112578000.00
Molecular weight molecular_weight83776.0 kDa
Excluded volume excluded_volume104800 ų
Envelope volume envelope_volume131500 ų
Hydration-shell volume shell_volume35824 ų
Envelope diameter envelope_diameter114.9
Shell Rg shell_rg37.49
Envelope Rg envelope_rg30.80
Shape Rg shape_rg30.93
Total Rg total_rg31.57
Total atoms total_atoms5878
Residues n_residues782
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 dmax103.9
Rg (real space) rg_real31.26
Rg uncertainty (real space) rg_real_error0.64
I(0) (real space) i0_real1.1260e+08
I(0) uncertainty (real space) i0_real_error1.4620e+06
Rg (reciprocal space) rg_reciprocal31.27
I(0) (reciprocal space) i0_reciprocal112600000.0000
Solution quality estimate total_estimate0.8876
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary32.6
Skewness Skewness skewness0.283
Kurtosis Kurtosis kurtosis-0.484
Angular range angular_range— – 0.2550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha70900000.0000
Real-space data points n_real_points52
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.886; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.936; Smooth: 0.942

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)