1qlc

Solution structure of the second PDZ domain of Postsynaptic Density-95

Method: SOLUTION NMR Dmax: 46.3 Å Quality: GOOD

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

POSTSYNAPTIC DENSITY PROTEIN 95

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 155–249 Fragment:THE SECOND PDZ DOMAIN No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6;303 K;Ionic strength (raw mmCIF value) 100;Pressure 1 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 SP90_RAT
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–95; UniProt 155–249

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 1qlc

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1qlc
Deposition date deposition_date1999-08-25
Structure title titleSolution structure of the second PDZ domain of Postsynaptic Density-95
Keywords keywordsPEPTIDE RECOGNITION, PDZ DOMAIN, NEURONAL NITRIC OXIDE SYNTHASE, NMDA RECEPTOR BINDING; PEPTIDE RECOGNITION
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier12.99
Radius of gyration Rg (electron density) rg_electron12.54
Forward intensity I(0) i0524094000.00
Molecular weight molecular_weight199370.0 kDa
Excluded volume excluded_volume252330 ų
Envelope volume envelope_volume20764 ų
Hydration-shell volume shell_volume12469 ų
Envelope diameter envelope_diameter48.5
Shell Rg shell_rg19.94
Envelope Rg envelope_rg14.64
Shape Rg shape_rg12.52
Total Rg total_rg12.76
Total atoms total_atoms28560
Residues n_residues1900
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 dmax46.3
Rg (real space) rg_real12.91
Rg uncertainty (real space) rg_real_error0.39
I(0) (real space) i0_real5.2410e+08
I(0) uncertainty (real space) i0_real_error6.2420e+06
Rg (reciprocal space) rg_reciprocal12.91
I(0) (reciprocal space) i0_reciprocal524100000.0000
Solution quality estimate total_estimate0.8563
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary17.0
Skewness Skewness skewness0.054
Kurtosis Kurtosis kurtosis-0.427
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha118000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.716; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.981; Smooth: 0.999

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_idd1qlca_
Class classb — All beta proteins
Fold Fold foldb.36 — PDZ domain-like
Superfamily Superfamily superfamilyb.36.1 — PDZ domain-like
Family Family familyb.36.1.1 — PDZ domain

CATH v4.4 (1 domains)

Domain ID domain_id1qlcA00
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)