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E. COLI thymidylate synthase in complex with BW1843U89 and 2'-deoxyuridine 5'-monophosphate (dump)

Analyse E. COLI thymidylate synthase in complex with BW1843U89 and 2'-deoxyuridine… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1SYN
Type
protein
Length
528 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
UMP, F89
Pockets
7 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 35% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BThymidylate synthase (EC 2.1.1.45)protein26435% helix, 25% strandP0A884

Ligands and binding sites

  • UMP · 2'-deoxyuridine 5'-monophosphate · ligand · 2 copies · chains A, B
  • F89 · S)-2-(5(((1,2-dihydro-3-methyl-1-oxobenzo(f)quinazolin-9-yl)methyl)amino)1-oxo-2-isoindolinyl)glutaric acid · ligand · 2 copies · chains A, B
  • FMT · Formic acid · additive · 2 copies · 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
14670.780.8646UMP, F89
24810.770.8548UMP, F89
31060.400.7619empty
4920.390.7718empty
5910.370.7618empty

Interfaces

1 interface between chains.

  • A–B · 2358 Ų buried · 38 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (additive adduct).

Compared structures

  • 1SYN · E. COLI thymidylate synthase in complex with BW1843U89 and 2'-deoxyuridine… · 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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