2naq

3D NMR solution structure of NLRP3 PYD

Method: SOLUTION NMR Dmax: 47.3 Å Quality: REASONABLE

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

NACHT, LRR and PYD domains-containing protein 3

Homo sapiens

UniProt Q96P20

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 3–93 Fragment:Pyrin domain residues 3-93 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 3.6;303 K;Ionic strength (raw mmCIF value) 0.0051;Pressure ambient NMR sample composition:100-200 uM [U-13C; U-15N] protein, 5 mM [U-2H] TCEP, 100 uM sodium azide, 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.

23 other PDB entries and 24 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NLRP3_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–91; UniProt 3–93

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 2naq

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2naq
Deposition date deposition_date2016-01-07
Structure title title3D NMR solution structure of NLRP3 PYD
Keywords keywordsDeath Domain Superfamily, APOPTOSIS; APOPTOSIS
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier13.78
Radius of gyration Rg (electron density) rg_electron13.47
Forward intensity I(0) i0625674000.00
Molecular weight molecular_weight212490.0 kDa
Excluded volume excluded_volume266270 ų
Envelope volume envelope_volume26756 ų
Hydration-shell volume shell_volume14655 ų
Envelope diameter envelope_diameter53.9
Shell Rg shell_rg21.42
Envelope Rg envelope_rg15.73
Shape Rg shape_rg13.39
Total Rg total_rg13.89
Total atoms total_atoms29820
Residues n_residues1820
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 dmax47.3
Rg (real space) rg_real13.67
Rg uncertainty (real space) rg_real_error0.29
I(0) (real space) i0_real6.2570e+08
I(0) uncertainty (real space) i0_real_error6.8220e+06
Rg (reciprocal space) rg_reciprocal13.68
I(0) (reciprocal space) i0_reciprocal625700000.0000
Solution quality estimate total_estimate0.6756
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary17.4
Skewness Skewness skewness0.005
Kurtosis Kurtosis kurtosis-0.256
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha258700.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.562; Stabil: 1.000; Sysdev: 0.368; Positv: 1.000; Valcen: 0.993; Smooth: 0.996

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_idd2naqa_
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.0 — automated matches

CATH v4.4 (1 domains)

Domain ID domain_id2naqA00
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)