2jvx

Solution Structure of human NEMO zinc finger

Method: SOLUTION NMR Dmax: 35.3 Å Quality: GOOD

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

NF-kappa-B essential modulator

OrganismNot specified

UniProt Q9Y6K9

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 394–419 Fragment:zinc finger domain ZN ZINC ION × 1 SOLUTION NMR NMR measurement conditions:pH 7.3;298 K;Ionic strength (raw mmCIF value) 0;Pressure ambient NMR sample composition:1 mM NEMO ZF, 2 mM ZnS04, 2 mM TCEP, 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.

11 other PDB entries and 20 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NEMO_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–28; UniProt 394–419

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 2jvx

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2jvx
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id2jvx
Deposition date deposition_date2007-09-28
Structure title titleSolution Structure of human NEMO zinc finger
Keywords keywords;CCHC classical zinc finger, NEMO zinc finger, beta-beta-alpha fold, Coiled coil, Cytoplasm, Disease mutation, Ectodermal dysplasia, Host-virus interaction, Nucleus, Transcription, Transcription regulation, METAL BINDING PROTEIN ;; METAL BINDING PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier8.58
Radius of gyration Rg (electron density) rg_electron8.59
Forward intensity I(0) i020616800.00
Molecular weight molecular_weight32970.0 kDa
Excluded volume excluded_volume39290 ų
Envelope volume envelope_volume7155 ų
Hydration-shell volume shell_volume6444 ų
Envelope diameter envelope_diameter35.2
Shell Rg shell_rg14.98
Envelope Rg envelope_rg10.51
Shape Rg shape_rg8.59
Total Rg total_rg8.98
Total atoms total_atoms4230
Residues n_residues280
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 dmax35.3
Rg (real space) rg_real8.61
Rg uncertainty (real space) rg_real_error0.58
I(0) (real space) i0_real2.0620e+07
I(0) uncertainty (real space) i0_real_error2.3130e+05
Rg (reciprocal space) rg_reciprocal8.61
I(0) (reciprocal space) i0_reciprocal20620000.0000
Solution quality estimate total_estimate0.7696
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary11.2
Skewness Skewness skewness0.368
Kurtosis Kurtosis kurtosis-0.061
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7960.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.518; Stabil: 0.995; Sysdev: 1.000; Positv: 1.000; Valcen: 0.483; Smooth: 0.977

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)