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Electron cryo-microscopy of chikungunya virus in complex with neutralizing antibody Fab CHK265

Analyse Electron cryo-microscopy of chikungunya virus in complex with neutralizing… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5ANY
Type
protein
Length
4,628 residues
Chains
16
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
E1; E2; Fab CHK265; Fab
UniProt
Q1H8W5
Pockets
20 · best druggability 0.70

Structure

electron microscopy · 4 distinct chains · 4% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, E, GE1protein3924% helix, 47% strandQ1H8W5
B, D, F, HE2protein3362% helix, 50% strandQ1H8W5
I, J, K, LFab CHK265protein2188% helix, 55% strand—
M, N, O, PFabprotein2114% helix, 56% strand—

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18090.700.7678empty
26080.650.7574empty
32760.610.7937empty
42500.590.7937empty
55180.580.7362empty

Interfaces

29 interfaces between chains.

  • E–F · 2522 Ų buried · 57 hydrogen bonds · protein-protein
  • G–H · 2522 Ų buried · 57 hydrogen bonds · protein-protein
  • C–D · 2522 Ų buried · 57 hydrogen bonds · protein-protein
  • A–B · 2513 Ų buried · 57 hydrogen bonds · protein-protein
  • I–M · 1865 Ų buried · 21 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 72 disulfide, 7 isopeptide (disulfide, isopeptide).

Compared structures

  • 5ANY · Electron cryo-microscopy of chikungunya virus in complex with neutralizing antibody Fab… · the same entry in another collection · chain A against A, TM-score 1.00

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