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Crystal structure of dutpase complexed with substrate analogue methylene-dutp

Analyse Crystal structure of dutpase complexed with substrate analogue methylene-dutp in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2HRM
Type
protein
Length
137 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Deoxyuridine 5'-triphosphate nucleotidohydrolase
EC
3.6.1.23
UniProt
P06968
Ligands
UC5
Pockets
1 · best druggability 0.42

Structure

x-ray diffraction · 1 distinct chain · 5% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADeoxyuridine 5'-triphosphate nucleotidohydrolase (EC 3.6.1.23)protein1375% helix, 42% strandP06968

Ligands and binding sites

  • UC5 · 2'-deoxy-5'-O-[(S)-hydroxy(phosphonomethyl)phosphoryl]uridine · ligand · chains A
  • EDO · 1,2-ethanediol · additive · chains A

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

Pockets

1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11120.420.7619empty

Compared structures

  • 2HRM · Crystal structure of dUTPase complexed with substrate analogue methylene-dUTP · the same entry in another collection · chain A against A, TM-score 1.00
  • P06968 · AlphaFold monomer V2.0 prediction for deoxyuridine 5'-triphosphate nucleotidohydrolase… · a predicted model of the same protein · chain A against A, TM-score 0.99

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