5vy2

Crystal structure of the F36A mutant of HsNUDT16

Method: X-RAY DIFFRACTION Dmax: 77.7 Å Quality: GOOD

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

U8 snoRNA-decapping enzyme

Homo sapiens

UniProt Q96DE0

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–195 Chain B; UniProt 1–195 Mutation:A22V, F36A NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 9.5;293 K;PEG 8000, CHES Resolution 2.30 Å R-free 0.253

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.

10 other PDB entries and 13 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NUD16_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–195; UniProt 1–195 Author chain B; PDBConstruct 1–195; UniProt 1–195

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 5vy2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5vy2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5vy2
Deposition date deposition_date2017-05-24
Structure title titleCrystal structure of the F36A mutant of HsNUDT16
Keywords keywords;nudix, nudix hydrolase, decapping enzyme, demodification of parylation, demodification of marylation, ADPribose, di-ADPribose, HYDROLASE ;; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.55
Radius of gyration Rg (electron density) rg_electron21.24
Forward intensity I(0) i026636800.00
Molecular weight molecular_weight39216.0 kDa
Excluded volume excluded_volume49109 ų
Envelope volume envelope_volume59083 ų
Hydration-shell volume shell_volume23373 ų
Envelope diameter envelope_diameter77.3
Shell Rg shell_rg28.21
Envelope Rg envelope_rg21.57
Shape Rg shape_rg21.24
Total Rg total_rg22.17
Total atoms total_atoms2766
Residues n_residues357
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 dmax77.7
Rg (real space) rg_real22.55
Rg uncertainty (real space) rg_real_error0.46
I(0) (real space) i0_real2.6640e+07
I(0) uncertainty (real space) i0_real_error3.4220e+05
Rg (reciprocal space) rg_reciprocal22.55
I(0) (reciprocal space) i0_reciprocal26640000.0000
Solution quality estimate total_estimate0.8626
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.9
Skewness Skewness skewness0.416
Kurtosis Kurtosis kurtosis-0.123
Angular range angular_range— – 0.3500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6117000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.746; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.991; Smooth: 0.980

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id5vy2A00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology79 — Nucleoside Triphosphate Pyrophosphohydrolase
Homologous superfamily homologous superfamily10 — Nucleoside Triphosphate Pyrophosphohydrolase
Domain ID domain_id5vy2B00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology79 — Nucleoside Triphosphate Pyrophosphohydrolase
Homologous superfamily homologous superfamily10 — Nucleoside Triphosphate Pyrophosphohydrolase

8. Citations (1)

9. Files and Curves (10)