1dbr

HYPOXANTHINE GUANINE XANTHINE

Method: X-RAY DIFFRACTION Dmax: 87.5 Å Quality: EXCELLENT

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

HYPOXANTHINE GUANINE XANTHINE PHOSPHORIBOSYLTRANSFERASE

Toxoplasma gondii

UniProt Q26997

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 1–230 Chain B; UniProt 1–230 Chain C; UniProt 1–230 Chain D; UniProt 1–230 Not recorded MG MAGNESIUM ION × 4 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.40 Å

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.

4 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name HGXR_TOXGO
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–230; UniProt 1–230 Author chain B; PDBConstruct 1–230; UniProt 1–230 Author chain C; PDBConstruct 1–230; UniProt 1–230 Author chain D; PDBConstruct 1–230; UniProt 1–230

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 1dbr

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1dbr
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1dbr
Deposition date deposition_date1996-02-13
Structure title titleHYPOXANTHINE GUANINE XANTHINE
Keywords keywordsTRANSFERASE, GLYCOSYLTRANSFERASE, PURINE SALVAGE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier29.15
Radius of gyration Rg (electron density) rg_electron27.75
Forward intensity I(0) i0150585000.00
Molecular weight molecular_weight100650.0 kDa
Excluded volume excluded_volume127440 ų
Envelope volume envelope_volume157310 ų
Hydration-shell volume shell_volume44737 ų
Envelope diameter envelope_diameter91.8
Shell Rg shell_rg37.18
Envelope Rg envelope_rg27.88
Shape Rg shape_rg27.73
Total Rg total_rg28.78
Total atoms total_atoms7107
Residues n_residues876
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 dmax87.5
Rg (real space) rg_real28.97
Rg uncertainty (real space) rg_real_error0.48
I(0) (real space) i0_real1.5060e+08
I(0) uncertainty (real space) i0_real_error2.2540e+06
Rg (reciprocal space) rg_reciprocal29.05
I(0) (reciprocal space) i0_reciprocal150600000.0000
Solution quality estimate total_estimate0.9017
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary38.9
Skewness Skewness skewness0.130
Kurtosis Kurtosis kurtosis-0.451
Angular range angular_range— – 0.2700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha88850000.0000
Real-space data points n_real_points55
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.930; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.972; Smooth: 0.957

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 8 domains

SCOP 2.08 (4 domains)

Domain ID domain_idd1dbra_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.61 — PRTase-like
Superfamily Superfamily superfamilyc.61.1 — PRTase-like
Family Family familyc.61.1.1 — Phosphoribosyltransferases (PRTases)
Domain ID domain_idd1dbrb_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.61 — PRTase-like
Superfamily Superfamily superfamilyc.61.1 — PRTase-like
Family Family familyc.61.1.1 — Phosphoribosyltransferases (PRTases)
Domain ID domain_idd1dbrc_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.61 — PRTase-like
Superfamily Superfamily superfamilyc.61.1 — PRTase-like
Family Family familyc.61.1.1 — Phosphoribosyltransferases (PRTases)
Domain ID domain_idd1dbrd_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.61 — PRTase-like
Superfamily Superfamily superfamilyc.61.1 — PRTase-like
Family Family familyc.61.1.1 — Phosphoribosyltransferases (PRTases)

CATH v4.4 (4 domains)

Domain ID domain_id1dbrA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily2020
Domain ID domain_id1dbrB00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily2020
Domain ID domain_id1dbrC00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily2020
Domain ID domain_id1dbrD00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily2020

8. Citations (1)

9. Files and Curves (10)