5ypo

Crystal structure of PSD-95 GK domain in complex with phospho-SAPAP peptide

Method: X-RAY DIFFRACTION Dmax: 85.0 Å Quality: REASONABLE

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

Disks large homolog 4

Rattus norvegicus

UniProt P31016

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 531–713 Not recorded SAPAP × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 5.5;289 K;Condition: 0.1 M Ammonium acetate, 0.1 M BIS-TRIS pH 5.5, 17% w/v Polyethylene glycol 10000 Resolution 2.29 Å R-free 0.226
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 531–713 Not recorded SAPAP × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 5.5;289 K;Condition: 0.1 M Ammonium acetate, 0.1 M BIS-TRIS pH 5.5, 17% w/v Polyethylene glycol 10000 Resolution 2.29 Å R-free 0.226

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.

40 other PDB entries and 57 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DLG4_RAT
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 7–189; UniProt 531–713 Author chain B; PDBConstruct 7–189; UniProt 531–713

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 5ypo

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5ypo
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5ypo
Deposition date deposition_date2017-11-02
Structure title titleCrystal structure of PSD-95 GK domain in complex with phospho-SAPAP peptide
Keywords keywordsPSD-95 SAPAP phosphorylation Synapse, PROTEIN BINDING; PROTEIN BINDING
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.96
Radius of gyration Rg (electron density) rg_electron25.25
Forward intensity I(0) i035469800.00
Molecular weight molecular_weight44386.0 kDa
Excluded volume excluded_volume55001 ų
Envelope volume envelope_volume69295 ų
Hydration-shell volume shell_volume24191 ų
Envelope diameter envelope_diameter87.3
Shell Rg shell_rg31.00
Envelope Rg envelope_rg25.05
Shape Rg shape_rg25.27
Total Rg total_rg25.86
Total atoms total_atoms3128
Residues n_residues390
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 dmax85.0
Rg (real space) rg_real26.07
Rg uncertainty (real space) rg_real_error0.53
I(0) (real space) i0_real3.5470e+07
I(0) uncertainty (real space) i0_real_error4.8520e+05
Rg (reciprocal space) rg_reciprocal26.04
I(0) (reciprocal space) i0_reciprocal35470000.0000
Solution quality estimate total_estimate0.7009
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary27.9
Skewness Skewness skewness0.462
Kurtosis Kurtosis kurtosis-0.352
Angular range angular_range— – 0.3050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6280000.0000
Real-space data points n_real_points62
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.857; Stabil: 1.000; Sysdev: 0.221; Positv: 1.000; Valcen: 0.936; Smooth: 0.939

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id5ypoA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases
Domain ID domain_id5ypoB00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases

8. Citations (1)

9. Files and Curves (10)