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Structure of POM1 Fab fragment complexed with human prpc fragment 120- 230

Analyse Structure of POM1 Fab fragment complexed with human prpc fragment 120- 230 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4DGI
Type
protein
Length
528 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Major prion protein; POM1 Fab heavy chain; POM1 Fab light chain
UniProt
P04156
Ligands
NA
Pockets
5 · best druggability 0.61

Structure

x-ray diffraction · 3 distinct chains · 17% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMajor prion proteinprotein9762% helix, 4% strandP04156
HPOM1 Fab heavy chainprotein2187% helix, 53% strand—
LPOM1 Fab light chainprotein2136% helix, 51% strand—

Ligands and binding sites

  • NA · Sodium ion · metal · chains L

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

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15350.610.7565empty
22350.510.7536empty
3600.280.7419empty
4640.280.7315empty
5520.280.7515empty

Interfaces

3 interfaces between chains.

  • H–L · 1717 Ų buried · 17 hydrogen bonds · protein-protein
  • A–H · 412 Ų buried · 9 hydrogen bonds · protein-protein
  • A–L · 256 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 4DGI · Structure of POM1 FAB fragment complexed with human PrPc Fragment 120-230 · the same entry in another collection · chain A against A, TM-score 1.00

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