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Crystal structure of syg-1 D1-D2, glycosylated

Analyse Crystal structure of syg-1 D1-D2, glycosylated in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OF3
Type
protein
Length
460 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein syg-1, isoform B
UniProt
B1Q236
Ligands
NAG, FUC, BMA
Pockets
4 · best druggability 0.62

Structure

x-ray diffraction · 2 distinct chains · 5% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein syg-1, isoform Bprotein2276% helix, 50% strandB1Q236
BProtein syg-1, isoform Bprotein2335% helix, 48% strandB1Q236

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A, B
  • FUC · alpha-L-fucopyranose · sugar · 3 copies · chains A
  • BMA · beta-D-mannopyranose · sugar

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12980.620.8043empty
21060.360.7420empty
3770.360.7617empty
4810.350.7619empty

Interfaces

1 interface between chains.

  • A–B · 904 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 3 glycan (disulfide, N-glycosylation).

Compared structures

  • 4OF3 · Crystal Structure of SYG-1 D1-D2, Glycosylated · the same entry in another collection · chain B against B, TM-score 1.00
  • B1Q236 · AlphaFold monomer V2.0 prediction for synaptogenesis protein syg-1 (B1Q236) · a predicted model of the same protein · chain A against A, TM-score 0.97

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