GL1X · GenesisL1 explorer

Research workbench

Crystal structure of the tricorn interacting factor F1 complex with pck

Analyse Crystal structure of the tricorn interacting factor F1 complex with pck in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1MU0
Type
protein
Length
293 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
PHK
Pockets
2 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 46% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProline iminopeptidase (EC 3.4.11.5)protein29346% helix, 18% strandP96084

Ligands and binding sites

  • PHK · (2R,3S)-3-amino-1-chloro-4-phenyl-butan-2-ol · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1790.760.9818PHK
21290.410.7519empty

Modifications

Observed in the structure: 1 covalent, 1 disulfide (covalent ligand, disulfide).

Compared structures

  • 1MU0 · Crystal Structure of the Tricorn Interacting Factor F1 Complex with PCK · 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

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.