2ka9

Solution structure of PSD-95 PDZ12 complexed with cypin peptide

Method: SOLUTION NMR Dmax: 79.7 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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 61–249 Fragment:N-terminal PDZ12 domain cypin peptide × 2 SOLUTION NMR NMR measurement conditions:pH 6.5;303 K;Ionic strength (raw mmCIF value) 100;Pressure ambient NMR sample composition:1mM [U-15N] PSD95 PDZ12, 1mM cypin peptide, 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.

40 other PDB entries and 58 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 1–189; UniProt 61–249

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 2ka9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2ka9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2ka9
Deposition date deposition_date2008-11-03
Structure title titleSolution structure of PSD-95 PDZ12 complexed with cypin peptide
Keywords keywords;PDZ-cypin peptide complex, tandem PDZ domain, Alternative splicing, Cell junction, Cell membrane, Lipoprotein, Membrane, Palmitate, Phosphoprotein, Postsynaptic cell membrane, SH3 domain, Synapse, CELL ADHESION ;; CELL ADHESION
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier23.59
Radius of gyration Rg (electron density) rg_electron23.71
Forward intensity I(0) i02643170000.00
Molecular weight molecular_weight439900.0 kDa
Excluded volume excluded_volume553030 ų
Envelope volume envelope_volume87915 ų
Hydration-shell volume shell_volume28548 ų
Envelope diameter envelope_diameter92.0
Shell Rg shell_rg33.16
Envelope Rg envelope_rg26.42
Shape Rg shape_rg23.71
Total Rg total_rg23.88
Total atoms total_atoms62540
Residues n_residues4140
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 dmax79.7
Rg (real space) rg_real23.79
Rg uncertainty (real space) rg_real_error0.64
I(0) (real space) i0_real2.6430e+09
I(0) uncertainty (real space) i0_real_error3.5800e+07
Rg (reciprocal space) rg_reciprocal23.74
I(0) (reciprocal space) i0_reciprocal2643000000.0000
Solution quality estimate total_estimate0.7063
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary18.7
Skewness Skewness skewness0.344
Kurtosis Kurtosis kurtosis-0.915
Angular range angular_range— – 0.3350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha40270000.0000
Real-space data points n_real_points65
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.290; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.348; Smooth: 0.960

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id2ka9A01
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology42 — Pdz3 Domain
Homologous superfamily homologous superfamily10 — PDZ domain
Domain ID domain_id2ka9A02
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology42 — Pdz3 Domain
Homologous superfamily homologous superfamily10 — PDZ domain

8. Citations (1)

9. Files and Curves (10)