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Structure of the L. blandensis dgtpase H125A mutant bound to dgtp and datp

Analyse Structure of the L. blandensis dgtpase H125A mutant bound to dgtp and datp in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7TU8
Type
protein
Length
2,604 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dgtp triphosphohydrolase
EC
3.1.5.1
UniProt
A3XHN1
Ligands
DGT, DTP, MG
Pockets
20 · best druggability 0.82

Structure

electron microscopy · 1 distinct chain · 65% helix, 2% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FDgtp triphosphohydrolase (EC 3.1.5.1)protein43465% helix, 2% strandA3XHN1

Ligands and binding sites

  • DGT · 2'-deoxyguanosine-5'-triphosphate · ligand · 6 copies · chains A, B, C, D, E, F
  • DTP · 2'-deoxyadenosine 5'-triphosphate · ligand · 6 copies · chains A, B, C, D, E, F
  • MG · Magnesium ion · metal · 12 copies · chains A, B, C, D, E, F

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

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13630.820.9144empty
23730.810.9043empty
33780.800.8942empty
4890.760.9720empty
51140.730.9327empty

Interfaces

9 interfaces between chains.

  • A–B · 1809 Ų buried · 10 hydrogen bonds · protein-protein
  • E–F · 1806 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 1802 Ų buried · 10 hydrogen bonds · protein-protein
  • A–E · 617 Ų buried · 5 hydrogen bonds · protein-protein
  • C–E · 615 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 7TU8 · Structure of the L. blandensis dGTPase H125A mutant bound to dGTP and dATP · the same entry in another collection · chain A against A, TM-score 1.00

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