1yme

STRUCTURE OF CARBOXYPEPTIDASE

Method: X-RAY DIFFRACTION Dmax: 63.8 Å Quality: REASONABLE

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

CARBOXYPEPTIDASE A ALPHA

OrganismNot specified

UniProt P00730

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 111–419 Not recorded ZN ZINC ION × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 1.53 Å

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.

29 other PDB entries and 45 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CBPA1_BOVIN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–309; UniProt 111–419

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 1yme

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1yme
Deposition date deposition_date1996-07-15
Structure title titleSTRUCTURE OF CARBOXYPEPTIDASE
Keywords keywordsCARBOXYPEPTIDASE, METALLOPROTEINASE, METALLOEXOPROTEINASE; CARBOXYPEPTIDASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.41
Radius of gyration Rg (electron density) rg_electron18.07
Forward intensity I(0) i019907700.00
Molecular weight molecular_weight34457.0 kDa
Excluded volume excluded_volume43192 ų
Envelope volume envelope_volume46977 ų
Hydration-shell volume shell_volume21042 ų
Envelope diameter envelope_diameter61.8
Shell Rg shell_rg25.14
Envelope Rg envelope_rg18.35
Shape Rg shape_rg18.04
Total Rg total_rg19.12
Total atoms total_atoms2437
Residues n_residues307
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 dmax63.8
Rg (real space) rg_real19.55
Rg uncertainty (real space) rg_real_error0.14
I(0) (real space) i0_real1.9520e+07
I(0) uncertainty (real space) i0_real_error1.7890e+05
Rg (reciprocal space) rg_reciprocal19.27
I(0) (reciprocal space) i0_reciprocal19910000.0000
Solution quality estimate total_estimate0.6780
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.1
Skewness Skewness skewness0.212
Kurtosis Kurtosis kurtosis-0.114
Angular range angular_range— – 0.4100 −1
Current regularization parameter α current_alpha7.2170
Highest regularization parameter α highest_alpha7019000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.800; Stabil: 0.932; Sysdev: 0.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.645

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1ymea_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.56 — Phosphorylase/hydrolase-like
Superfamily Superfamily superfamilyc.56.5 — Zn-dependent exopeptidases
Family Family familyc.56.5.1 — Pancreatic carboxypeptidases

CATH v4.4 (1 domains)

Domain ID domain_id1ymeA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology630 — Aminopeptidase
Homologous superfamily homologous superfamily10 — Zn peptidases

8. Citations (1)

9. Files and Curves (10)