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Crystal structure of HIV protease complexed with methyl N-[(1S)-1- benzhydryl-2-[2-[2-[(2R,5S)-5-(BENZYLCARBAMOYLOXYMETHYL)MORPHOLIN-2- YL]ETHYL]ANILINO]-2-oxo-ETHYL]CARBAMATE

Analyse Crystal structure of HIV protease complexed with methyl N-[(1S)-1… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5IVS
Type
protein
Length
198 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protease
UniProt
Q77VV3
Ligands
6EF, CL
Pockets
1 · best druggability 0.71

Structure

x-ray diffraction · 1 distinct chain · 7% helix, 54% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BProteaseprotein997% helix, 54% strandQ77VV3

Ligands and binding sites

  • 6EF · N-(2-{2-[(2R,5S)-5-{[(benzylcarbamoyl)oxy]methyl}morpholin-2-yl]ethyl}phenyl)-Nalpha-(methoxycarbonyl)-beta-phenyl-L-phenylalaninamide · ligand · chains A, B
  • CL · Chloride ion · ion · 3 copies · chains A, B

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
13830.710.82386EF

Interfaces

1 interface between chains.

  • A–B · 1854 Ų buried · 39 hydrogen bonds · protein-protein

Compared structures

  • 5IVS · Crystal Structure of HIV Protease complexed with methyl… · the same entry in another collection · chain A against A, TM-score 1.00

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