2kyk

The sandwich region between two LMP2A PY motif regulates the interaction between AIP4WW2domain and PY motif

Method: SOLUTION NMR Dmax: 32.2 Å Quality: REASONABLE

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

E3 ubiquitin-protein ligase Itchy homolog

Homo sapiens

UniProt Q96J02

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 359–392 Fragment:WW 2 domain No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6;303 K;Pressure ambient NMR sample composition:0.01% [U-95% 13C; U-95% 15N] sodium phosphate-1, 90% H2O/10% D2O | 90% H2O/10% D2O 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.

11 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ITCH_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 6–39; UniProt 359–392

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 2kyk

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2kyk
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2kyk
Deposition date deposition_date2010-05-28
Structure title titleThe sandwich region between two LMP2A PY motif regulates the interaction between AIP4WW2domain and PY motif
Keywords keywordsLMP2A, PY motif, Ubiquitin-protein ligase, WW domain, LIGASE; LIGASE
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier12.37
Radius of gyration Rg (electron density) rg_electron12.27
Forward intensity I(0) i0135533000.00
Molecular weight molecular_weight93286.0 kDa
Excluded volume excluded_volume115110 ų
Envelope volume envelope_volume20669 ų
Hydration-shell volume shell_volume11486 ų
Envelope diameter envelope_diameter56.7
Shell Rg shell_rg20.88
Envelope Rg envelope_rg16.72
Shape Rg shape_rg12.15
Total Rg total_rg12.98
Total atoms total_atoms12940
Residues n_residues780
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 dmax32.2
Rg (real space) rg_real11.72
Rg uncertainty (real space) rg_real_error0.05
I(0) (real space) i0_real1.2950e+08
I(0) uncertainty (real space) i0_real_error1.0190e+06
Rg (reciprocal space) rg_reciprocal12.48
I(0) (reciprocal space) i0_reciprocal135500000.0000
Solution quality estimate total_estimate0.6756
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks0
Primary peak position r_peak_primary
Skewness Skewness skewness0.162
Kurtosis Kurtosis kurtosis-0.759
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha6.0400
Highest regularization parameter α highest_alpha22150.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.001; Oscil: 0.993; Stabil: 0.966; Sysdev: 0.000; Positv: 1.000; Valcen: 0.910; 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 (2 domains)

Domain ID domain_idd2kyka1
Class classb — All beta proteins
Fold Fold foldb.72 — WW domain-like
Superfamily Superfamily superfamilyb.72.1 — WW domain
Family Family familyb.72.1.1 — WW domain
Domain ID domain_idd2kyka2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

8. Citations (1)

9. Files and Curves (10)