1pn5

NMR structure of the NALP1 Pyrin domain (PYD)

Method: SOLUTION NMR Dmax: 50.9 Å Quality: REASONABLE

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

NACHT-, LRR- and PYD-containing protein 2

Homo sapiens

UniProt P06654

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 228–282 Fragment:Pyrin domain (PYD) No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.5;293 K;Pressure 1 NMR sample composition:1mM NALP1 PYD U-15N,13C; 50mM Na / PO4 - Buffer; 50mM NaCl; 1mM CHAPS; 20mM DTT (D10); 0.02% NaN3; 0.1mM EDTA; protease inhibitor cocktail (Complete, Roche); 95% H2O, 5% D2O | 95% H2O/5% 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.

48 other PDB entries and 54 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SPG1_STRSG
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–56; UniProt 228–282

NACHT-, LRR- and PYD-containing protein 2

Homo sapiens

UniProt Q9C000

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–93 Fragment:Pyrin domain (PYD) No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.5;293 K;Pressure 1 NMR sample composition:1mM NALP1 PYD U-15N,13C; 50mM Na / PO4 - Buffer; 50mM NaCl; 1mM CHAPS; 20mM DTT (D10); 0.02% NaN3; 0.1mM EDTA; protease inhibitor cocktail (Complete, Roche); 95% H2O, 5% D2O | 95% H2O/5% 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 18 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NAL1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 59–151; UniProt 1–93

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 1pn5

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1pn5
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1pn5
Deposition date deposition_date2003-06-12
Structure title titleNMR structure of the NALP1 Pyrin domain (PYD)
Keywords keywords5 ALPHA-HELIX BUNDLE, APOPTOSIS; APOPTOSIS
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier13.84
Radius of gyration Rg (electron density) rg_electron13.13
Forward intensity I(0) i0629460000.00
Molecular weight molecular_weight204470.0 kDa
Excluded volume excluded_volume252580 ų
Envelope volume envelope_volume32713 ų
Hydration-shell volume shell_volume16432 ų
Envelope diameter envelope_diameter56.8
Shell Rg shell_rg22.82
Envelope Rg envelope_rg17.12
Shape Rg shape_rg13.10
Total Rg total_rg13.47
Total atoms total_atoms28220
Residues n_residues1860
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 dmax50.9
Rg (real space) rg_real13.79
Rg uncertainty (real space) rg_real_error0.48
I(0) (real space) i0_real6.2950e+08
I(0) uncertainty (real space) i0_real_error7.7960e+06
Rg (reciprocal space) rg_reciprocal13.80
I(0) (reciprocal space) i0_reciprocal629500000.0000
Solution quality estimate total_estimate0.7186
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary18.0
Skewness Skewness skewness0.309
Kurtosis Kurtosis kurtosis0.126
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha541800.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.456; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.972; 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_idd1pn5a1
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.5 — Pyrin domain, PYD

CATH v4.4 (1 domains)

Domain ID domain_id1pn5A00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas

8. Citations (1)

9. Files and Curves (10)