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Structural implications of drug resistant mutants of HIV-1 protease: high resolution crystal structures of the mutant PROTEASE/SUBSTRATE analog complexes

Analyse Structural implications of drug resistant mutants of HIV-1 protease: high… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1FGC
Type
protein
Length
198 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protease retropepsin
EC
3.4.23.16
UniProt
P04587
Ligands
2NC
Pockets
1 · best druggability 0.70

Structure

x-ray diffraction · 1 distinct chain · 4% helix, 58% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
C, DProtease retropepsin (EC 3.4.23.16)protein994% helix, 58% strandP04587

Ligands and binding sites

  • 2NC · N-{(2S)-2-[(N-acetyl-L-threonyl-L-isoleucyl)amino]hexyl}-L-norleucyl-L-glutaminyl-N~5~-[amino(iminio)methyl]-L-ornithinamide · ligand · chains C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13560.700.82372NC

Interfaces

1 interface between chains.

  • C–D · 1849 Ų buried · 41 hydrogen bonds · protein-protein

Compared structures

  • 1FGC · Structural implications of drug resistant mutants of HIV-1 protease: high resolution… · the same entry in another collection · chain D against D, TM-score 1.00

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