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Partial Structure of the C-terminal domain of the HPIV4B phosphoprotein, fused to MBP.

Analyse Partial Structure of the C-terminal domain of the HPIV4B phosphoprotein, fused… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4KYD
Type
protein
Length
801 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.21
Source
Escherichia coli; Human parainfluenza virus 4b
Molecule
Maltose-binding periplasmic protein, Phosphoprotein, chimeric construct
UniProt
P0AEX9, P21738
Ligands
GLC
Pockets
6 · best druggability 0.72

Structure

x-ray diffraction · resolution 2.21 · 2 distinct chains · 49% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMaltose-binding periplasmic protein, Phosphoprotein, chimeric constructprotein40148% helix, 19% strandP0AEX9, P21738
BMaltose-binding periplasmic protein, Phosphoprotein, chimeric constructprotein40050% helix, 20% strandP0AEX9, P21738

Ligands and binding sites

  • GLC · alpha-D-glucopyranose · sugar · 4 copies · chains A, B
  • MPO · 3[N-morpholino]propane sulfonic acid · additive · 6 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19200.720.7671empty
22650.710.8530GLC
32660.700.8529GLC, MPO
42670.530.7526empty
52630.510.7532empty

Interfaces

1 interface between chains.

  • A–B · 870 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 4KYD · Partial structure of the C-terminal domain of the HPIV4B phosphoprotein, fused to mbp. · the same entry in another collection · chain A against A, TM-score 1.00

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