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Crystal structure of clade A/E 93TH057 HIV-1 GP120 core in complex with mae-II-167

Analyse Crystal structure of clade A/E 93TH057 HIV-1 GP120 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
4DVW
Type
protein
Length
678 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Clade A/E 93TH057 HIV-1 GP120 core
UniProt
A0A0M3KKW9
Ligands
0M4, NAG
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 18% helix, 38% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BClade A/E 93TH057 HIV-1 GP120 coreprotein33918% helix, 38% strandA0A0M3KKW9

Ligands and binding sites

  • 0M4 · N-(4-chloro-3-fluorophenyl)-N'-[(3aS,6aS)-hexahydrocyclopenta[c]pyrrol-3a(1H)-ylmethyl]ethanediamide · ligand · 2 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 20 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

6 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18020.760.80102NAG
21200.640.88290M4
3890.600.88220M4
4640.510.8518NAG
5540.400.8220empty

Interfaces

1 interface between chains.

  • A–B · 472 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 20 glycan, 14 disulfide (N-glycosylation, disulfide).

Compared structures

  • 4DVW · Crystal structure of clade A/E 93TH057 HIV-1 gp120 core in complex with MAE-II-167 · the same entry in another collection · chain A against A, TM-score 1.00

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