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Alpha-N-acetylgalactosaminidase nagbb from bifidobacterium bifidum - galnac complex

Analyse Alpha-N-acetylgalactosaminidase nagbb from bifidobacterium bifidum - galnac… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5WZN
Type
protein
Length
1,240 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-N-acetylgalactosaminidase
EC
3.2.1.49
UniProt
G5ELM1
Ligands
A2G, ZN, CA
Pockets
17 · best druggability 0.89

Structure

x-ray diffraction · 2 distinct chains · 23% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAlpha-N-acetylgalactosaminidase (EC 3.2.1.49)protein62124% helix, 33% strandG5ELM1
BAlpha-N-acetylgalactosaminidase (EC 3.2.1.49)protein61922% helix, 33% strandG5ELM1

Ligands and binding sites

  • A2G · 2-acetamido-2-deoxy-alpha-D-galactopyranose · sugar · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110440.890.90105empty
2570.660.9423empty
33000.620.8050A2G
42420.590.8040A2G
51040.450.7924empty

Interfaces

1 interface between chains.

  • A–B · 2066 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 5WZN · Alpha-N-acetylgalactosaminidase NagBb from Bifidobacterium bifidum - GalNAc complex · the same entry in another collection · chain A against A, TM-score 1.00

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