GL1X · GenesisL1 explorer

Research workbench

Crystal structure of dipeptidyl peptidase 11 (DPP11) from porphyromonas gingivalis

Analyse Crystal structure of dipeptidyl peptidase 11 (DPP11) from porphyromonas… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Y01
Type
protein
Length
1,398 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peptidase S46
UniProt
A0A076NW73
Pockets
11 · best druggability 0.72

Structure

x-ray diffraction · 1 distinct chain · 51% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPeptidase S46protein69951% helix, 16% strandA0A076NW73

Ligands and binding sites

  • GOL · Glycerol · additive · chains A

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

Pockets

11 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18460.720.7783empty
26270.670.7655GOL
32600.560.7727empty
44100.550.7362empty
51320.390.7419empty

Interfaces

1 interface between chains.

  • A–B · 811 Ų buried · 24 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 46 modified, 2 disulfide (engineered, disulfide).

Compared structures

  • 4Y01 · Crystal structure of dipeptidyl peptidase 11 (DPP11) from Porphyromonas gingivalis · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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