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S268Y variant of jc polyomavirus major capsid protein VP1

Analyse S268Y variant of jc polyomavirus major capsid protein VP1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4JCD
Type
protein
Length
1,285 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Major capsid protein VP1
UniProt
P03089
Pockets
15 · best druggability 0.51

Structure

x-ray diffraction · 3 distinct chains · 9% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, D, EMajor capsid protein VP1protein2578% helix, 42% strandP03089
BMajor capsid protein VP1protein2588% helix, 42% strandP03089
CMajor capsid protein VP1protein2569% helix, 42% strandP03089

Ligands and binding sites

  • GOL · Glycerol · additive · 5 copies · chains A, E, B, C, D
  • EDO · 1,2-ethanediol · additive · 3 copies · chains A, D, E

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13170.510.7435empty
22130.510.7630empty
32330.500.7528EDO
41390.500.8028empty
51910.500.7740empty

Interfaces

5 interfaces between chains.

  • C–D · 2366 Ų buried · 43 hydrogen bonds · protein-protein
  • D–E · 2353 Ų buried · 45 hydrogen bonds · protein-protein
  • A–B · 2329 Ų buried · 45 hydrogen bonds · protein-protein
  • B–C · 2322 Ų buried · 49 hydrogen bonds · protein-protein
  • A–E · 2320 Ų buried · 43 hydrogen bonds · protein-protein

Compared structures

  • 4JCD · S268Y Variant of JC Polyomavirus Major Capsid Protein VP1 · the same entry in another collection · chain A against A, TM-score 1.00

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