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Crystal structure of E. COLI thymidylate synthase complexed with sp- 876

Analyse Crystal structure of E. COLI thymidylate synthase complexed with sp- 876 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1F4G
Type
protein
Length
523 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thymidylate synthase
EC
2.1.1.45
UniProt
P0A884
Ligands
TP4, SO4
Pockets
7 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThymidylate synthase (EC 2.1.1.45)protein26234% helix, 27% strandP0A884
BThymidylate synthase (EC 2.1.1.45)protein26136% helix, 27% strandP0A884

Ligands and binding sites

  • TP4 · N-[4-[[glutamic acid]-carbonyl]-benzene-sulfonyl-D-prolinyl]-3-amino-propanoic acid · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 4 copies · chains A, B
  • GOL · Glycerol · additive · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15000.720.8251SO4, TP4
25740.690.7851GOL, TP4
31180.410.7619empty
41090.400.7617empty
5510.380.8114empty

Interfaces

1 interface between chains.

  • A–B · 2250 Ų buried · 30 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (carboxylation, oxidation).

Compared structures

  • 1F4G · Crystal structure of E. COLI thymidylate synthase complexed with sp-876 · the same entry in another collection · chain A against A, TM-score 1.00
  • P0A884 · AlphaFold monomer V2.0 prediction for thymidylate synthase (P0A884) · a predicted model of the same protein · chain B against A, TM-score 0.99

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