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MolNFT v1 · #139201 · protein

Crystal structure of ATP-tmp and ADP bound thymidylate kinase from thermus thermophilus HB8

5X8B: “Crystal structure of ATP-tmp and ADP bound thymidylate kinase from thermus thermophilus HB8”. X-ray diffraction, 4 ligands (ATP, TMP, ADP), 4 pockets (best druggability 0.53). MolNFT v1 #139201 on GenesisL1: 3D structure, binding…

PDB
5X8B
Type
protein
Length
376 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
ATP, TMP, ADP, MG
Pockets
4 · best druggability 0.53

Structure

x-ray diffraction · 2 distinct chains · 53% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThymidylate kinase (EC 2.7.4.9)protein18952% helix, 14% strandQ5SHX3
BThymidylate kinase (EC 2.7.4.9)protein18754% helix, 15% strandQ5SHX3

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · chains A
  • TMP · Thymidine-5'-phosphate · ligand · chains A
  • ADP · Adenosine-5'-diphosphate · ligand · chains B
  • MG · Magnesium ion · metal · 7 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
11880.530.7828TMP, MG
21590.500.7823MG
3680.440.8217empty
4580.390.8014empty

Interfaces

1 interface between chains.

  • A–B · 1044 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 5X8B · Crystal structure of ATP-TMP and ADP bound thymidylate kinase from Thermus thermophilus… · 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 A against A, TM-score 0.98

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