6gls

Crystal structure of hMTH1 N33G in complex with TH scaffold 1 in the absence of acetate

Method: X-RAY DIFFRACTION Dmax: 72.6 Å Quality: GOOD

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

7,8-dihydro-8-oxoguanine triphosphatase

Homo sapiens

UniProt P36639

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 42–197 Not recorded F3E 4-phenylpyrimidin-2-amine × 2 SO4 SULFATE ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.5;293 K;crystallized in: 23-27% PEG3350, 0.2 M LiSO4, 0.1 M sodium acetate pH 4.5 soaked in: 0.27 M ammonium sulfate, 17% glycerol, 27% PEG4000, 50 mM compound Resolution 1.50 Å R-free 0.199
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 42–197 Not recorded F3E 4-phenylpyrimidin-2-amine × 1 SO4 SULFATE ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.5;293 K;crystallized in: 23-27% PEG3350, 0.2 M LiSO4, 0.1 M sodium acetate pH 4.5 soaked in: 0.27 M ammonium sulfate, 17% glycerol, 27% PEG4000, 50 mM compound Resolution 1.50 Å R-free 0.199

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.

123 other PDB entries and 204 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name 8ODP_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 27–182; UniProt 42–197 Author chain B; PDBConstruct 27–182; UniProt 42–197

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 6gls

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6gls
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6gls
Deposition date deposition_date2018-05-23
Structure title titleCrystal structure of hMTH1 N33G in complex with TH scaffold 1 in the absence of acetate
Keywords keywordsInhibitor, Complex, Hydrolase, DNA repair, Fragment; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.93
Radius of gyration Rg (electron density) rg_electron21.26
Forward intensity I(0) i021918700.00
Molecular weight molecular_weight35521.0 kDa
Excluded volume excluded_volume44251 ų
Envelope volume envelope_volume52195 ų
Hydration-shell volume shell_volume21220 ų
Envelope diameter envelope_diameter74.3
Shell Rg shell_rg26.96
Envelope Rg envelope_rg21.32
Shape Rg shape_rg21.24
Total Rg total_rg22.07
Total atoms total_atoms2500
Residues n_residues314
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 dmax72.6
Rg (real space) rg_real21.98
Rg uncertainty (real space) rg_real_error0.45
I(0) (real space) i0_real2.1920e+07
I(0) uncertainty (real space) i0_real_error2.8990e+05
Rg (reciprocal space) rg_reciprocal21.97
I(0) (reciprocal space) i0_reciprocal21920000.0000
Solution quality estimate total_estimate0.8710
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary23.8
Skewness Skewness skewness0.466
Kurtosis Kurtosis kurtosis-0.202
Angular range angular_range— – 0.3600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8423000.0000
Real-space data points n_real_points68
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.791; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.967; Smooth: 0.979

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (4 domains)

Domain ID domain_idd6glsa1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.113 — Nudix
Superfamily Superfamily superfamilyd.113.1 — Nudix
Family Family familyd.113.1.1 — MutT-like
Domain ID domain_idd6glsa2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags
Domain ID domain_idd6glsb1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.113 — Nudix
Superfamily Superfamily superfamilyd.113.1 — Nudix
Family Family familyd.113.1.1 — MutT-like
Domain ID domain_idd6glsb2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (2 domains)

Domain ID domain_id6glsA00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology79 — Nucleoside Triphosphate Pyrophosphohydrolase
Homologous superfamily homologous superfamily10 — Nucleoside Triphosphate Pyrophosphohydrolase
Domain ID domain_id6glsB00
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)