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Crystal structure of active site F1-mutant E245Q soaked with peptide phe-leu

Analyse Crystal structure of active site F1-mutant E245Q soaked with peptide phe-leu in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1XRQ
Type
protein
Length
290 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proline iminopeptidase
EC
3.4.11.5
UniProt
P96084
Ligands
LEU
Pockets
3 · best druggability 0.71

Structure

x-ray diffraction · 1 distinct chain · 49% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProline iminopeptidase (EC 3.4.11.5)protein29049% helix, 18% strandP96084

Ligands and binding sites

  • LEU · Leucine · ligand · chains A

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

Pockets

3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1510.710.9819LEU
21710.550.7929empty
3510.270.7414empty

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 1XRQ · Crystal structure of active site F1-mutant E245Q soaked with peptide Phe-Leu · the same entry in another collection · chain A against A, TM-score 1.00
  • P96084 · AlphaFold monomer V2.0 prediction for proline iminopeptidase (P96084) · a predicted model of the same protein · chain A against A, TM-score 0.99

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