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Coxsackievirus A24V in complex with the D1-D2 fragment of icam-1

Analyse Coxsackievirus A24V in complex with the D1-D2 fragment of icam-1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6EIT
Type
protein
Length
860 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
VP1; VP2; VP3; Intercellular adhesion molecule 1
UniProt
G3C8J7, A0A088F913, Q0GYP7, P05362
Pockets
6 · best druggability 0.79

Structure

electron microscopy · 4 distinct chains · 7% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
1VP1protein28010% helix, 29% strandG3C8J7
2VP2protein2648% helix, 33% strandA0A088F913
3VP3protein2316% helix, 29% strandQ0GYP7
4Intercellular adhesion molecule 1protein850% helix, 38% strandP05362

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16200.790.8479empty
22660.640.8230empty
34160.640.7848empty
42120.500.7625empty
5700.320.7519empty

Interfaces

6 interfaces between chains.

  • 1–2 · 2378 Ų buried · 41 hydrogen bonds · protein-protein
  • 1–3 · 1477 Ų buried · 18 hydrogen bonds · protein-protein
  • 2–3 · 795 Ų buried · 12 hydrogen bonds · protein-protein
  • 1–4 · 712 Ų buried · 10 hydrogen bonds · protein-protein
  • 2–4 · 368 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 6EIT · Coxsackievirus A24v in complex with the D1-D2 fragment of ICAM-1 · the same entry in another collection · chain 1 against 1, TM-score 1.00
  • P05362 · AlphaFold monomer V2.0 prediction for intercellular adhesion molecule 1 (P05362) · a predicted model of the same protein · chain 4 against A, TM-score 0.92

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