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Herpes simplex virus type-I thymidine kinase complexed with a novel non-substrate inhibitor, 9-(4-hydroxybutyl)-N2- phenylguanine

Analyse Herpes simplex virus type-I thymidine kinase complexed with a novel… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1QHI
Type
protein
Length
604 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein (thymidine kinase)
EC
2.7.1.21
UniProt
P03176
Ligands
BPG, SO4
Pockets
9 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 57% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein (thymidine kinase) (EC 2.7.1.21)protein30057% helix, 13% strandP03176
BProtein (thymidine kinase) (EC 2.7.1.21)protein30457% helix, 13% strandP03176

Ligands and binding sites

  • BPG · 9-(4-hydroxybutyl)-N2-phenylguanine · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B

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

Pockets

9 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11310.810.9820BPG
21290.800.9720BPG
31520.600.8327empty
41230.480.7923empty
51210.470.7921empty

Interfaces

1 interface between chains.

  • A–B · 1731 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 1QHI · Herpes simplex virus type-I thymidine kinase complexed with a novel non-substrate… · the same entry in another collection · chain A against A, TM-score 1.00

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