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Mouse thymidylate synthase cocrystallized with N(4)OHDCMP and soaked in methylenetetrahydrofolate

Analyse Mouse thymidylate synthase cocrystallized with N(4)OHDCMP and soaked in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6F6Z
Type
protein
Length
574 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thymidylate synthase
EC
2.1.1.45
UniProt
P07607
Ligands
NOH, TGQ
Pockets
8 · best druggability 0.77

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BThymidylate synthase (EC 2.1.1.45)protein28734% helix, 23% strandP07607

Ligands and binding sites

  • NOH · 2'-deoxy-N-hydroxycytidine 5'-(dihydrogen phosphate) · ligand · 2 copies · chains A, B
  • TGQ · (2~{S})-2-[[4-[[(6~{R})-2-azanyl-4-oxidanylidene-5,6,7,8-tetrahydro-1~{H}-pteridin-6-yl]methyl-methyl-amino]phenyl]carbonylamino]pentanedioic acid · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14540.770.8549NOH, TGQ
24620.770.8545NOH, TGQ
31490.480.7720empty
4980.460.7916empty
5800.390.7815empty

Interfaces

1 interface between chains.

  • A–B · 2190 Ų buried · 39 hydrogen bonds · protein-protein

Compared structures

  • 6F6Z · Mouse Thymidylate Synthase Cocrystallized with N(4)OHdCMP and Soaked in… · the same entry in another collection · chain A against A, TM-score 1.00
  • P07607 · AlphaFold monomer V2.0 prediction for thymidylate synthase (P07607) · a predicted model of the same protein · chain B against A, TM-score 0.99

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