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Crystal structure of Dscam1 isoform 4.44, N-terminal four Ig domains

Analyse Crystal structure of Dscam1 isoform 4.44, N-terminal four Ig domains in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4X9B
Type
protein
Length
775 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.2
Source
Drosophila melanogaster
Molecule
Down syndrome cell adhesion molecule, isoform 4.44
Ligands
NAG, BMA, MAN, NA
Pockets
9 · best druggability 0.80

Structure

x-ray diffraction · resolution 2.2 · 2 distinct chains · 5% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADown syndrome cell adhesion molecule, isoform 4.44protein3925% helix, 52% strand—
BDown syndrome cell adhesion molecule, isoform 4.44protein3835% helix, 47% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A, B
  • BMA · beta-D-mannopyranose · sugar · 2 copies
  • MAN · alpha-D-mannopyranose · sugar · chains A
  • NA · Sodium ion · metal · 2 copies · chains A

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

Pockets

9 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111150.800.82115empty
22590.670.8447empty
3910.640.9027empty
41050.450.7819empty
51000.430.7819empty

Interfaces

1 interface between chains.

  • A–B · 1603 Ų buried · 21 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 4X9B · Crystal structure of DSCAM1 isoform 4.44, N-terminal four ig domains · the same entry in another collection · chain A against A, TM-score 1.00

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