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Cyclic hexapeptide pkidnp in complex with HIV-1 integrase

Analyse Cyclic hexapeptide pkidnp in complex with HIV-1 integrase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3WNG
Type
protein
Length
286 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Gag-pol polyprotein; PKIDN(DPR) peptide
UniProt
P12497
Ligands
CD, SO4, CL
Pockets
3 · best druggability 0.54

Structure

x-ray diffraction · 3 distinct chains · 49% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGag-pol polyproteinprotein13851% helix, 20% strandP12497
BGag-pol polyproteinprotein13650% helix, 20% strandP12497
C, DPKIDN(DPR) peptideprotein60% helix, 33% strand—

Ligands and binding sites

  • CD · Cadmium ion · metal · 4 copies · chains A, B
  • SO4 · Sulfate ion · ion · 6 copies · chains A, B
  • CL · Chloride ion · ion · 2 copies · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12010.540.7821empty
21060.470.8026empty
3840.410.7824empty

Interfaces

5 interfaces between chains.

  • A–B · 1529 Ų buried · 21 hydrogen bonds · protein-protein
  • B–C · 243 Ų buried · 6 hydrogen bonds · protein-protein
  • A–D · 241 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 166 Ų buried · 2 hydrogen bonds · protein-protein
  • B–D · 165 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 d-amino (D-amino acid).

Compared structures

  • 3WNG · Cyclic hexapeptide PKIDNp in complex with HIV-1 integrase · the same entry in another collection · chain C against C, TM-score 1.00

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