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Hypoxanthine phosphoribosyltransferase from trypanosoma cruzi, in complex with the product imp

Analyse Hypoxanthine phosphoribosyltransferase from trypanosoma cruzi, in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1P19
Type
protein
Length
742 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hypoxanthine phosphoribosyltransferase
EC
2.4.2.8
UniProt
Q27796
Ligands
IMP
Pockets
11 · best druggability 0.62

Structure

x-ray diffraction · 4 distinct chains · 27% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHypoxanthine phosphoribosyltransferase (EC 2.4.2.8)protein18724% helix, 33% strandQ27796
BHypoxanthine phosphoribosyltransferase (EC 2.4.2.8)protein18432% helix, 32% strandQ27796
CHypoxanthine phosphoribosyltransferase (EC 2.4.2.8)protein18526% helix, 31% strandQ27796
DHypoxanthine phosphoribosyltransferase (EC 2.4.2.8)protein18628% helix, 33% strandQ27796

Ligands and binding sites

  • IMP · Inosinic acid · ligand · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12000.620.8323empty
23760.610.7737IMP
32980.610.7937empty
43200.590.7733IMP
53760.580.7539IMP

Interfaces

3 interfaces between chains.

  • A–B · 1755 Ų buried · 22 hydrogen bonds · protein-protein
  • C–D · 1703 Ų buried · 23 hydrogen bonds · protein-protein
  • A–C · 313 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 1P19 · Hypoxanthine Phosphoribosyltransferase from Trypanosoma cruzi, in complex with the… · the same entry in another collection · chain A against A, TM-score 1.00

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