6cdz

E. coli thymidylate synthase mutant I264Am

Method: X-RAY DIFFRACTION Dmax: 74.6 Å Quality: REASONABLE

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 1–263 Chain B; UniProt 1–263 Fragment:residues 1-263 Non-standard monomer:Yes (specific site not provided by mmCIF) CB3 10-PROPARGYL-5,8-DIDEAZAFOLIC ACID × 2 UMP 2'-DEOXYURIDINE 5'-MONOPHOSPHATE × 1 UMC 2'-deoxy-5'-uridylic acid × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;295 K;100 mM HEPES, 200 mM NH4Ac, 5mM DTT, 32% PEG 4000 (W/V) Resolution 2.40 Å R-free 0.229

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 1–263; UniProt 1–263 Author chain B; PDBConstruct 1–263; UniProt 1–263

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 6cdz

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id6cdz
Deposition date deposition_date2018-02-09
Structure title titleE. coli thymidylate synthase mutant I264Am
Keywords keywordsTRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier24.29
Radius of gyration Rg (electron density) rg_electron22.96
Forward intensity I(0) i064691400.00
Molecular weight molecular_weight62376.0 kDa
Excluded volume excluded_volume77689 ų
Envelope volume envelope_volume88562 ų
Hydration-shell volume shell_volume30836 ų
Envelope diameter envelope_diameter74.3
Shell Rg shell_rg31.31
Envelope Rg envelope_rg23.22
Shape Rg shape_rg22.95
Total Rg total_rg23.87
Total atoms total_atoms8543
Residues n_residues524
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 dmax74.6
Rg (real space) rg_real24.13
Rg uncertainty (real space) rg_real_error0.39
I(0) (real space) i0_real6.4690e+07
I(0) uncertainty (real space) i0_real_error7.8840e+05
Rg (reciprocal space) rg_reciprocal24.17
I(0) (reciprocal space) i0_reciprocal64690000.0000
Solution quality estimate total_estimate0.7173
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.8
Skewness Skewness skewness0.179
Kurtosis Kurtosis kurtosis-0.397
Angular range angular_range— – 0.3250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha16580000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.910; Stabil: 0.999; Sysdev: 0.264; Positv: 1.000; Valcen: 0.990; Smooth: 0.810

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd6cdza_
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
Domain ID domain_idd6cdzb_
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

CATH v4.4 (2 domains)

Domain ID domain_id6cdzA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology572 — Thymidylate Synthase; Chain A
Homologous superfamily homologous superfamily10 — Thymidylate synthase/dCMP hydroxymethylase domain
Domain ID domain_id6cdzB00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology572 — Thymidylate Synthase; Chain A
Homologous superfamily homologous superfamily10 — Thymidylate synthase/dCMP hydroxymethylase domain

8. Citations (2)

9. Files and Curves (10)