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Fmdv capsid in complex with M170 nab

Analyse Fmdv capsid in complex with M170 nab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7DST
Type
protein
Length
772 residues
Chains
5
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
VP1 of O type fmdv capsid; VP2 of O type fmdv capsid; VP3 of O type fmdv capsid; VP4 of O…
Pockets
8 · best druggability 0.76

Structure

electron microscopy · 5 distinct chains · 10% helix, 36% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AVP1 of O type fmdv capsidprotein18415% helix, 30% strand—
BVP2 of O type fmdv capsidprotein2068% helix, 45% strand—
CVP3 of O type fmdv capsidprotein2198% helix, 33% strand—
DVP4 of O type fmdv capsidprotein4622% helix, 0% strand—
EM170 nabprotein1175% helix, 53% strand—

Pockets

8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19690.760.79114empty
25430.680.7852empty
34070.670.8039empty
42140.630.8228empty
51480.460.7723empty

Interfaces

8 interfaces between chains.

  • A–B · 1314 Ų buried · 16 hydrogen bonds · protein-protein
  • A–C · 1013 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 926 Ų buried · 6 hydrogen bonds · protein-protein
  • A–D · 790 Ų buried · 12 hydrogen bonds · protein-protein
  • C–E · 739 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 7DST · FMDV capsid in complex with M170 Nab · the same entry in another collection · chain A against A, TM-score 1.00

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