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HROBO2 ectodomain

Analyse HROBO2 ectodomain in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6IAA
Type
protein
Length
2,445 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Roundabout homolog 2
UniProt
Q9HCK4
Ligands
NAG, MAN, BMA
Pockets
19 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 3% helix, 44% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CRoundabout homolog 2protein8153% helix, 44% strandQ9HCK4

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 12 copies · chains A, B, C
  • MAN · alpha-D-mannopyranose · sugar · 6 copies · chains A, B, C
  • BMA · beta-D-mannopyranose · sugar · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110040.790.81101empty
211780.750.7893empty
32860.600.7934empty
43190.600.7839empty
52630.580.7834empty

Interfaces

2 interfaces between chains.

  • B–C · 712 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 402 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 33 modified, 15 disulfide, 6 glycan (engineered, disulfide, N-glycosylation).

Compared structures

  • 6IAA · hRobo2 ectodomain · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9HCK4 · AlphaFold monomer V2.0 prediction for roundabout homolog 2 (Q9HCK4) · a predicted model of the same protein · chain A against A, TM-score 0.96

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