5ao4

Crystal structure of in vitro phosphorylated human SAMHD1 (amino acid residues 115-626) bound to GTP

Method: X-RAY DIFFRACTION Dmax: 114.9 Å Quality: EXCELLENT

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

DEOXYNUCLEOSIDE TRIPHOSPHATE TRIPHOSPHOHYDROLASE SAMHD1

HOMO SAPIENS

UniProt Q9Y3Z3

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 115–626 Chain B; UniProt 115–626 Chain C; UniProt 115–626 Chain D; UniProt 115–626 Fragment:RESIDUES 115-626 FE FE (III) ION × 4 GTP GUANOSINE-5'-TRIPHOSPHATE × 4 X-RAY DIFFRACTION X-ray crystallization conditions:0.2 M SODIUM FORMATE, 20% PEG 3350 Resolution 3.70 Å R-free 0.308

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.

75 other PDB entries and 105 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SAMH1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 27–538; UniProt 115–626 Author chain B; PDBConstruct 27–538; UniProt 115–626 Author chain C; PDBConstruct 27–538; UniProt 115–626 Author chain D; PDBConstruct 27–538; UniProt 115–626

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 5ao4

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5ao4
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5ao4
Deposition date deposition_date2015-09-09
Structure title titleCrystal structure of in vitro phosphorylated human SAMHD1 (amino acid residues 115-626) bound to GTP
Keywords keywordsHYDROLASE, DEOXYNUCLEOSIDE TRIPHOSPHATE TRIPHOSPHOHYDROLASE, HIV RESTRICTION FACTOR; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier36.76
Radius of gyration Rg (electron density) rg_electron36.15
Forward intensity I(0) i0473269000.00
Molecular weight molecular_weight173280.0 kDa
Excluded volume excluded_volume214580 ų
Envelope volume envelope_volume285360 ų
Hydration-shell volume shell_volume62972 ų
Envelope diameter envelope_diameter115.0
Shell Rg shell_rg44.82
Envelope Rg envelope_rg35.68
Shape Rg shape_rg36.15
Total Rg total_rg36.68
Total atoms total_atoms12222
Residues n_residues1625
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 dmax114.9
Rg (real space) rg_real36.56
Rg uncertainty (real space) rg_real_error0.80
I(0) (real space) i0_real4.7330e+08
I(0) uncertainty (real space) i0_real_error6.8280e+06
Rg (reciprocal space) rg_reciprocal36.69
I(0) (reciprocal space) i0_reciprocal473300000.0000
Solution quality estimate total_estimate0.9022
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary45.4
Skewness Skewness skewness0.151
Kurtosis Kurtosis kurtosis-0.542
Angular range angular_range— – 0.2150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha95500000.0000
Real-space data points n_real_points44
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.928; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.991; Smooth: 0.949

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 4 domains

CATH v4.4 (4 domains)

Domain ID domain_id5ao4A01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3210 — Hypothetical protein af1432
Homologous superfamily homologous superfamily10 — Hypothetical protein af1432
Domain ID domain_id5ao4B01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3210 — Hypothetical protein af1432
Homologous superfamily homologous superfamily10 — Hypothetical protein af1432
Domain ID domain_id5ao4C01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3210 — Hypothetical protein af1432
Homologous superfamily homologous superfamily10 — Hypothetical protein af1432
Domain ID domain_id5ao4D01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3210 — Hypothetical protein af1432
Homologous superfamily homologous superfamily10 — Hypothetical protein af1432

8. Citations (1)

9. Files and Curves (10)