5ep6

The crystal structure of NAP1 in complex with TBK1

Method: X-RAY DIFFRACTION Dmax: 66.3 Å Quality: GOOD

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

5-azacytidine-induced protein 2

Homo sapiens

UniProt Q9H6S1

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 215–255 Fragment:UNP RESIDUES 215-255 Serine/threonine-protein kinase TBK1 × 1 (Q9UHD2) GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;291.15 K;1% w/v Tryptone, 0.05 M HEPES sodium (pH 7.0), 12% w/v PEG 3350 Resolution 1.45 Å R-free 0.217
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 215–255 Fragment:UNP RESIDUES 215-255 Serine/threonine-protein kinase TBK1 × 1 (Q9UHD2) GOL GLYCEROL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;291.15 K;1% w/v Tryptone, 0.05 M HEPES sodium (pH 7.0), 12% w/v PEG 3350 Resolution 1.45 Å R-free 0.217

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.

3 other PDB entries and 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name AZI2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–41; UniProt 215–255 Author chain C; PDBConstruct 1–41; UniProt 215–255

Serine/threonine-protein kinase TBK1

Homo sapiens

UniProt Q9UHD2

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 677–729 Fragment:UNP RESIDUES 677-729 5-azacytidine-induced protein 2 × 1 (Q9H6S1) GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;291.15 K;1% w/v Tryptone, 0.05 M HEPES sodium (pH 7.0), 12% w/v PEG 3350 Resolution 1.45 Å R-free 0.217
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 677–729 Fragment:UNP RESIDUES 677-729 5-azacytidine-induced protein 2 × 1 (Q9H6S1) GOL GLYCEROL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;291.15 K;1% w/v Tryptone, 0.05 M HEPES sodium (pH 7.0), 12% w/v PEG 3350 Resolution 1.45 Å R-free 0.217

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.

24 other PDB entries and 27 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TBK1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 6–58; UniProt 677–729 Author chain D; PDBConstruct 6–58; UniProt 677–729

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 5ep6

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5ep6
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5ep6
Deposition date deposition_date2015-11-11
Structure title titleThe crystal structure of NAP1 in complex with TBK1
Keywords keywordsNAP1, TBK1, CALCOCO2, PROTEIN BINDING-TRANSFERASE complex; PROTEIN BINDING/TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.40
Radius of gyration Rg (electron density) rg_electron18.65
Forward intensity I(0) i07130480.00
Molecular weight molecular_weight19105.0 kDa
Excluded volume excluded_volume23807 ų
Envelope volume envelope_volume28476 ų
Hydration-shell volume shell_volume13882 ų
Envelope diameter envelope_diameter64.9
Shell Rg shell_rg23.25
Envelope Rg envelope_rg19.17
Shape Rg shape_rg18.63
Total Rg total_rg19.46
Total atoms total_atoms1329
Residues n_residues163
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 dmax66.3
Rg (real space) rg_real19.61
Rg uncertainty (real space) rg_real_error0.51
I(0) (real space) i0_real7.1300e+06
I(0) uncertainty (real space) i0_real_error9.0170e+04
Rg (reciprocal space) rg_reciprocal19.58
I(0) (reciprocal space) i0_reciprocal7130000.0000
Solution quality estimate total_estimate0.7979
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary17.7
Skewness Skewness skewness0.581
Kurtosis Kurtosis kurtosis-0.250
Angular range angular_range— – 0.4100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3466000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.615; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.688; Smooth: 0.838

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)