2vet

CRYSTAL STRUCTURE OF THE THYMIDYLATE SYNTHASE K48Q COMPLEXED WITH DUMP

Method: X-RAY DIFFRACTION Dmax: 59.9 Å Quality: EXCELLENT

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

THYMIDYLATE SYNTHASE

ESCHERICHIA COLI

UniProt P0A884

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 1–264 Mutation:YES Non-standard monomer:Yes (specific site not provided by mmCIF) UMP 2'-DEOXYURIDINE 5'-MONOPHOSPHATE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7.5;20 MM POTASSIUM PHOSPHATE BUFFER, 4 MM DTT AND INCREMENTS IN AMMONIUM SULFATE FROM 2.05 TO 2.6 M, PH 7.5 TO 8 Resolution 2.20 Å R-free 0.205

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.

56 other PDB entries and 63 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TYSY_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–264; UniProt 1–264

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 2vet

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2vet
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2vet
Deposition date deposition_date2007-10-26
Structure title titleCRYSTAL STRUCTURE OF THE THYMIDYLATE SYNTHASE K48Q COMPLEXED WITH DUMP
Keywords keywords;REPRESSOR, CYTOPLASM, RNA-BINDING, TRANSFERASE, NUCLEOTIDE BIOSYNTHESIS, DUMP SUBSTRATE, METHYLTRANSFERASE, THYMIDYLATE SYNTHASE, TRANSLATION REGULATION ;; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.82
Radius of gyration Rg (electron density) rg_electron18.31
Forward intensity I(0) i016920100.00
Molecular weight molecular_weight30806.0 kDa
Excluded volume excluded_volume38384 ų
Envelope volume envelope_volume44730 ų
Hydration-shell volume shell_volume20101 ų
Envelope diameter envelope_diameter59.8
Shell Rg shell_rg24.92
Envelope Rg envelope_rg18.49
Shape Rg shape_rg18.30
Total Rg total_rg19.29
Total atoms total_atoms2172
Residues n_residues263
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 dmax59.9
Rg (real space) rg_real19.65
Rg uncertainty (real space) rg_real_error0.29
I(0) (real space) i0_real1.6920e+07
I(0) uncertainty (real space) i0_real_error1.9180e+05
Rg (reciprocal space) rg_reciprocal19.68
I(0) (reciprocal space) i0_reciprocal16920000.0000
Solution quality estimate total_estimate0.9065
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.2
Skewness Skewness skewness0.068
Kurtosis Kurtosis kurtosis-0.494
Angular range angular_range— – 0.4000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2903000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.932; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.986; Smooth: 0.998

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 1 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2veta_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.117 — Thymidylate synthase/dCMP hydroxymethylase
Superfamily Superfamily superfamilyd.117.1 — Thymidylate synthase/dCMP hydroxymethylase
Family Family familyd.117.1.1 — Thymidylate synthase/dCMP hydroxymethylase

8. Citations (1)

9. Files and Curves (10)