1v6d

The crystal structure of the trypsin complex with synthetic heterochiral peptide

Method: X-RAY DIFFRACTION Dmax: 55.5 Å Quality: REASONABLE

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 9–231 Not recorded PD(AIB)L(AIB)LA × 1 CA CALCIUM ION × 1 ACT ACETATE ION × 1 TBF TERT-BUTYL FORMATE × 1 NME METHYLAMINE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.4;293 K;2M ammonium sulphate, pH 6.4, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 1.90 Å R-free 0.178

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 54 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 1–223; UniProt 9–231

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 1v6d

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1v6d
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1v6d
Deposition date deposition_date2003-11-28
Structure title titleThe crystal structure of the trypsin complex with synthetic heterochiral peptide
Keywords keywordsTrypsin complex, synthetic peptide, hydrolase; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier17.44
Radius of gyration Rg (electron density) rg_electron16.44
Forward intensity I(0) i011334700.00
Molecular weight molecular_weight24393.0 kDa
Excluded volume excluded_volume30231 ų
Envelope volume envelope_volume33565 ų
Hydration-shell volume shell_volume16880 ų
Envelope diameter envelope_diameter56.1
Shell Rg shell_rg22.76
Envelope Rg envelope_rg16.70
Shape Rg shape_rg16.43
Total Rg total_rg17.44
Total atoms total_atoms1704
Residues n_residues225
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 dmax55.5
Rg (real space) rg_real17.31
Rg uncertainty (real space) rg_real_error0.35
I(0) (real space) i0_real1.1330e+07
I(0) uncertainty (real space) i0_real_error1.3420e+05
Rg (reciprocal space) rg_reciprocal17.33
I(0) (reciprocal space) i0_reciprocal11330000.0000
Solution quality estimate total_estimate0.6348
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary22.2
Skewness Skewness skewness0.123
Kurtosis Kurtosis kurtosis-0.439
Angular range angular_range— – 0.4550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2949000.0000
Real-space data points n_real_points76
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.846; Stabil: 0.995; Sysdev: 0.242; Positv: 1.000; Valcen: 0.997; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1v6da_
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 (2 domains)

Domain ID domain_id1v6dA01
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases
Domain ID domain_id1v6dA02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology10 — Thrombin, subunit H
Homologous superfamily homologous superfamily10 — Trypsin-like serine proteases

8. Citations (1)

9. Files and Curves (10)