GL1X · GenesisL1 explorer

MolNFT v1 · #139200 · protein

Crystal structure of ATP bound thymidylate kinase from thermus thermophilus HB8

5X8A: “Crystal structure of ATP bound thymidylate kinase from thermus thermophilus HB8”. X-ray diffraction, 3 ligands (ATP, MG, CL), 4 pockets (best druggability 0.69). MolNFT v1 #139200 on GenesisL1: 3D structure, binding sites and…

PDB
5X8A
Type
protein
Length
386 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, MG, CL
Pockets
4 · best druggability 0.69

Structure

x-ray diffraction · 2 distinct chains · 53% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThymidylate kinase (EC 2.7.4.9)protein19751% helix, 14% strandQ5SHX3
BThymidylate kinase (EC 2.7.4.9)protein18955% helix, 14% strandQ5SHX3

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · chains B
  • MG · Magnesium ion · metal · 3 copies · chains A, B
  • CL · Chloride ion · ion · 5 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · 2 copies · chains 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15000.690.7941MG
2520.390.8116empty
3650.340.7711empty
4540.310.7714empty

Interfaces

1 interface between chains.

  • A–B · 432 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 5X8A · Crystal structure of ATP bound thymidylate kinase from thermus thermophilus HB8 · 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

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.