1omu

SOLUTION STRUCTURE OF OVOMUCOID (THIRD DOMAIN) FROM DOMESTIC TURKEY (298K, PH 4.1) (NMR, 50 STRUCTURES) (REFINED MODEL USING NETWORK EDITING ANALYSIS)

Method: SOLUTION NMR Dmax: 30.2 Å Quality: GOOD

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

OVOMUCOID (THIRD DOMAIN)

Meleagris gallopavo

UniProt P68390

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 130–185 Not recorded No other associated polymer SOLUTION NMR mmCIF provides none of the parsed experimental conditions Resolution not provided

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.

36 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name IOVO_MELGA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–56; UniProt 130–185

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 1omu

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1omu
Deposition date deposition_date1995-10-11
Structure title titleSOLUTION STRUCTURE OF OVOMUCOID (THIRD DOMAIN) FROM DOMESTIC TURKEY (298K, PH 4.1) (NMR, 50 STRUCTURES) (REFINED MODEL USING NETWORK EDITING ANALYSIS)
Keywords keywordsSPIN DIFFUSION, NETWORK EDITING, BD-NOESY, CBD-NOESY, SERINE PROTEINASE INHIBITOR; SERINE PROTEINASE INHIBITOR
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier10.05
Radius of gyration Rg (electron density) rg_electron10.36
Forward intensity I(0) i01406130000.00
Molecular weight molecular_weight301040.0 kDa
Excluded volume excluded_volume368790 ų
Envelope volume envelope_volume15916 ų
Hydration-shell volume shell_volume10553 ų
Envelope diameter envelope_diameter41.5
Shell Rg shell_rg18.55
Envelope Rg envelope_rg13.53
Shape Rg shape_rg10.34
Total Rg total_rg10.52
Total atoms total_atoms40700
Residues n_residues2800
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 dmax30.2
Rg (real space) rg_real9.97
Rg uncertainty (real space) rg_real_error0.25
I(0) (real space) i0_real1.4060e+09
I(0) uncertainty (real space) i0_real_error1.3300e+07
Rg (reciprocal space) rg_reciprocal9.97
I(0) (reciprocal space) i0_reciprocal1406000000.0000
Solution quality estimate total_estimate0.8355
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary13.4
Skewness Skewness skewness-0.079
Kurtosis Kurtosis kurtosis-0.721
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha22720.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.953; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1omua_
Class classg — Small proteins
Fold Fold foldg.68 — Kazal-type serine protease inhibitors
Superfamily Superfamily superfamilyg.68.1 — Kazal-type serine protease inhibitors
Family Family familyg.68.1.1 — Ovomucoid domain III-like

CATH v4.4 (1 domains)

Domain ID domain_id1omuA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology60 — Wheat Germ Agglutinin (Isolectin 2); domain 1
Homologous superfamily homologous superfamily30

8. Citations (3)

9. Files and Curves (10)