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Coxsackievirus B3 full particle at PH7.4 (VP3-234Q)

Analyse Coxsackievirus B3 full particle at PH7.4 (VP3-234Q) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7VXH
Type
protein
Length
819 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Capsid protein VP1; Capsid protein VP2; Capsid protein VP3; Capsid protein VP4
UniProt
P03313
Ligands
PLM
Pockets
10 · best druggability 0.79

Structure

electron microscopy · 4 distinct chains · 11% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACapsid protein VP1protein26810% helix, 29% strandP03313
BCapsid protein VP2protein25611% helix, 34% strandP03313
CCapsid protein VP3protein23811% helix, 31% strandP03313
DCapsid protein VP4protein5711% helix, 16% strandP03313

Ligands and binding sites

  • PLM · Palmitic acid · ligand · chains A, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15900.790.8574PLM
2870.520.8427empty
31490.470.7729empty
41350.470.7821empty
5860.460.8129empty

Interfaces

6 interfaces between chains.

  • A–C · 4326 Ų buried · 56 hydrogen bonds · protein-protein
  • A–B · 2151 Ų buried · 27 hydrogen bonds · protein-protein
  • B–C · 1656 Ų buried · 12 hydrogen bonds · protein-protein
  • A–D · 1165 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 889 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 7VXH · Coxsackievirus B3 full particle at pH7.4 (VP3-234Q) · the same entry in another collection · chain A against A, TM-score 1.00

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