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Crystal structure of the outer domain of HIV-1 GP120 in complex with vrc-PG04 space group P3221

Analyse Crystal structure of the outer domain of HIV-1 GP120 in complex with vrc-PG04… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4I3R
Type
protein
Length
626 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Outer domain of HIV-1 GP120 (KER2018 OD4.2.2); Heavy chain of vrc-PG04 Fab; Light chain…
Ligands
NAG
Pockets
8 · best druggability 0.59

Structure

x-ray diffraction · 3 distinct chains · 9% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
GOuter domain of HIV-1 GP120 (KER2018 OD4.2.2)protein19011% helix, 37% strand—
HHeavy chain of vrc-PG04 Fabprotein22810% helix, 50% strand—
LLight chain of vrc-PG04 Fabprotein2087% helix, 51% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains G

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

8 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12170.590.8131empty
23290.540.7447empty
31840.460.7629empty
41070.400.7618empty
51190.400.7524empty

Interfaces

3 interfaces between chains.

  • H–L · 1901 Ų buried · 13 hydrogen bonds · protein-protein
  • G–H · 950 Ų buried · 18 hydrogen bonds · protein-protein
  • G–L · 188 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 9 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 4I3R · Crystal structure of the outer domain of HIV-1 gp120 in complex with VRC-PG04 space group… · the same entry in another collection · chain G against G, TM-score 1.00

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