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Crystal structure of nelfinavir-resistant, inactive HIV-1 protease (D30N/N88D) in complex with the P1-P6 substrate variant (L449F/S451N)

Analyse Crystal structure of nelfinavir-resistant, inactive HIV-1 protease (D30N/N88D)… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OBD
Type
protein
Length
413 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HIV-1 protease; P1-P6 peptide
EC
3.4.23.16
UniProt
P03369, P03349
Pockets
3 · best druggability 0.48

Structure

x-ray diffraction · 3 distinct chains · 5% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DHIV-1 protease (EC 3.4.23.16)protein996% helix, 56% strandP03369
EP1-P6 peptideprotein90% helix, 33% strandP03349
FP1-P6 peptideprotein80% helix, 38% strandP03349

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 3 copies · chains B, D, C, A, E
  • GOL · Glycerol · additive · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1580.480.8620empty
21470.420.7522empty
3950.350.7425empty

Interfaces

11 interfaces between chains.

  • A–B · 1818 Ų buried · 37 hydrogen bonds · protein-protein
  • C–D · 1742 Ų buried · 36 hydrogen bonds · protein-protein
  • B–E · 611 Ų buried · 12 hydrogen bonds · protein-protein
  • C–F · 512 Ų buried · 10 hydrogen bonds · protein-protein
  • A–E · 492 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 4OBD · Crystal Structure of Nelfinavir-Resistant, Inactive HIV-1 Protease (D30N/N88D) in Complex… · the same entry in another collection · chain A against A, TM-score 1.00

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