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MDR769 HIV-1 protease complexed with CA/P2 hepta-peptide

Analyse MDR769 HIV-1 protease complexed with CA/P2 hepta-peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3OUD
Type
protein
Length
205 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Mdr HIV-1 protease; CA/P2 substrate peptide
UniProt
Q000H7
Pockets
1 · best druggability 0.65

Structure

x-ray diffraction · 3 distinct chains · 7% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMdr HIV-1 proteaseprotein997% helix, 52% strandQ000H7
BMdr HIV-1 proteaseprotein997% helix, 53% strandQ000H7
PCA/P2 substrate peptideprotein70% helix, 0% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14880.650.7738empty

Interfaces

3 interfaces between chains.

  • A–B · 1542 Ų buried · 36 hydrogen bonds · protein-protein
  • B–P · 480 Ų buried · 12 hydrogen bonds · protein-protein
  • A–P · 254 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 3OUD · MDR769 HIV-1 protease complexed with CA/p2 hepta-peptide · the same entry in another collection · chain A against A, TM-score 1.00

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