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Crystal structures of multidrug-resistant clinical isolate 769 HIV-1 protease variants

Analyse Crystal structures of multidrug-resistant clinical isolate 769 HIV-1 protease… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3OQ7
Type
protein
Length
99 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HIV-1 protease
UniProt
Q000H7
Pockets
1 · best druggability 0.47

Structure

x-ray diffraction · 1 distinct chain · 7% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHIV-1 proteaseprotein997% helix, 46% strandQ000H7

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11410.470.7720empty

Compared structures

  • 3OQ7 · Crystal Structures of Multidrug-Resistant Clinical Isolate 769 HIV-1 Protease Variants · the same entry in another collection · chain A against A, TM-score 1.00

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