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Pre-fusion structure of trimeric HIV-1 envelope glycoprotein determined by cryo-electron microscopy

Analyse Pre-fusion structure of trimeric HIV-1 envelope glycoprotein determined by… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4CC8
Type
protein
Length
2,430 residues
Chains
12
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
GP41; GP120; Monoclonal antibody VRC03 Fab heavy chain; Monoclonal antibody VRC03 Fab…
Pockets
20 · best druggability 0.73

Structure

electron microscopy · 4 distinct chains · 15% helix, 44% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CGP41protein3194% helix, 0% strand—
D, E, GGP120protein34419% helix, 39% strand—
F, H, IMonoclonal antibody VRC03 Fab heavy chainprotein2279% helix, 51% strand—
J, K, LMonoclonal antibody VRC03 Fab light chainprotein2085% helix, 51% strand—

Pockets

20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15900.730.8055empty
26090.720.8052empty
35900.720.8052empty
43800.570.7547empty
53460.560.7545empty

Interfaces

15 interfaces between chains.

  • F–J · 1725 Ų buried · 11 hydrogen bonds · protein-protein
  • H–L · 1723 Ų buried · 11 hydrogen bonds · protein-protein
  • I–K · 1721 Ų buried · 11 hydrogen bonds · protein-protein
  • E–H · 1060 Ų buried · 14 hydrogen bonds · protein-protein
  • D–F · 1058 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 15 disulfide (disulfide).

Compared structures

  • 4CC8 · Pre-fusion structure of trimeric HIV-1 envelope glycoprotein determined by cryo-electron… · the same entry in another collection · chain A against A, TM-score 1.00

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