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Crystal structure of thymidylate kinase in complex with ADP, tdp and tmp from thermus thermophilus HB8

Analyse Crystal structure of thymidylate kinase in complex with ADP, tdp and tmp from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5ZAX
Type
protein
Length
377 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thymidylate kinase
EC
2.7.4.9
UniProt
Q5SHX3
Ligands
ADP, TYD, TMP, MG, CL
Pockets
4 · best druggability 0.59

Structure

x-ray diffraction · 2 distinct chains · 54% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThymidylate kinase (EC 2.7.4.9)protein19054% helix, 15% strandQ5SHX3
BThymidylate kinase (EC 2.7.4.9)protein18753% helix, 15% strandQ5SHX3

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · chains A
  • TYD · Thymidine-5'-diphosphate · ligand · chains A
  • TMP · Thymidine-5'-phosphate · ligand · chains B
  • MG · Magnesium ion · metal · 8 copies · chains A, B
  • CL · Chloride ion · ion · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12030.590.8132MG, TYD
23010.580.7738TMP, CL
3630.420.8116CL
4500.350.7914empty

Interfaces

1 interface between chains.

  • A–B · 1070 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 5ZAX · Crystal structure of thymidylate kinase in complex with ADP, TDP and TMP from thermus… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q5SHX3 · AlphaFold monomer V2.0 prediction for thymidylate kinase (Q5SHX3) · a predicted model of the same protein · chain B against A, TM-score 0.98

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