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Crystal structure of clade A/E 93TH057 HIV-1 GP120 H375S core in complex with dmj-II-121

Analyse Crystal structure of clade A/E 93TH057 HIV-1 GP120 H375S core in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4I54
Type
protein
Length
678 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HIV-1 glycoprotein
Ligands
1C1, NAG
Pockets
10 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 19% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHIV-1 glycoproteinprotein33919% helix, 37% strand—

Ligands and binding sites

  • 1C1 · amino({[(1R,2R)-1-({[(4-chloro-3-fluorophenyl)amino](oxo)acetyl}amino)-2,3-dihydro-1H-inden-2-yl]methyl}amino)methanimi nium · ligand · 2 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 16 copies · chains A, B
  • EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · 2 copies · chains A, B

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

Pockets

10 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17420.750.8089NAG
2790.620.90221C1
3620.610.9120empty
4880.560.86191C1
5590.550.8818NAG

Interfaces

1 interface between chains.

  • A–B · 502 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 15 glycan, 14 disulfide (N-glycosylation, disulfide).

Compared structures

  • 4I54 · Crystal structure of clade A/E 93TH057 HIV-1 gp120 H375S core in complex with DMJ-II-121 · the same entry in another collection · chain A against A, TM-score 1.00

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