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Endo-glycoceramidase II from rhodococcus sp.: lactosyl-enzyme intermediate

Analyse Endo-glycoceramidase II from rhodococcus sp.: lactosyl-enzyme intermediate in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2OSY
Type
protein
Length
867 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Endoglycoceramidase II
EC
3.2.1.123
UniProt
O33853
Ligands
GLC, GAL, NA
Pockets
11 · best druggability 0.66

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEndoglycoceramidase II (EC 3.2.1.123)protein43232% helix, 22% strandO33853
BEndoglycoceramidase II (EC 3.2.1.123)protein43532% helix, 22% strandO33853

Ligands and binding sites

  • GLC · alpha-D-glucopyranose · sugar · 2 copies · chains A, B
  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B

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

Pockets

11 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16530.660.7569NA
24360.650.7850GLC, GAL
31430.630.8519empty
41410.620.8517empty
52640.570.7729GLC, GAL

Interfaces

1 interface between chains.

  • A–B · 448 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 glycan (glycosylation).

Compared structures

  • 2OSY · Endo-glycoceramidase II from Rhodococcus sp.: Lactosyl-Enzyme Intermediate · the same entry in another collection · chain A against A, TM-score 1.00

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