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Cryo-EM structure of the BG505 SOSIP.664 HIV-1 env trimer with 3 PGV04 fabs

Analyse Cryo-EM structure of the BG505 SOSIP.664 HIV-1 env trimer with 3 PGV04 fabs in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3J5M
Type
protein
Length
2,733 residues
Chains
12
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
BG505 sosip GP120; BG505 sosip GP41; PGV04 light chain; PGV04 heavy chain
UniProt
Q2N0S6
Pockets
20 · best druggability 0.83

Structure

electron microscopy · 4 distinct chains · 17% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, E, IBG505 sosip GP120protein41514% helix, 31% strandQ2N0S6
B, F, JBG505 sosip GP41protein6394% helix, 0% strand—
C, G, KPGV04 light chainprotein2087% helix, 49% strand—
D, H, LPGV04 heavy chainprotein2259% helix, 48% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15470.830.8968empty
27050.810.8581empty
32500.760.9035empty
46240.760.8282empty
53160.760.8846empty

Interfaces

21 interfaces between chains.

  • C–D · 1966 Ų buried · 13 hydrogen bonds · protein-protein
  • K–L · 1963 Ų buried · 13 hydrogen bonds · protein-protein
  • G–H · 1962 Ų buried · 13 hydrogen bonds · protein-protein
  • E–H · 961 Ų buried · 16 hydrogen bonds · protein-protein
  • I–L · 959 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 39 disulfide (disulfide).

Compared structures

  • 3J5M · Cryo-EM structure of the BG505 SOSIP.664 HIV-1 Env trimer with 3 PGV04 Fabs · the same entry in another collection · chain A against A, TM-score 1.00

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