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High resolution structures of HIV-1 rt from four rt- inhibitor complexes

Analyse High resolution structures of HIV-1 rt from four rt- inhibitor complexes in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1VRT
Type
protein
Length
926 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HIV-1 reverse transcriptase
EC
2.7.7.49
UniProt
P04585
Ligands
NVP, MG
Pockets
15 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 34% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHIV-1 reverse transcriptase (EC 2.7.7.49)protein52532% helix, 22% strandP04585
BHIV-1 reverse transcriptase (EC 2.7.7.49)protein40136% helix, 20% strandP04585

Ligands and binding sites

  • NVP · 11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3,2-B:2',3'-e][1,4]diazepin-6-one · ligand · chains A
  • MG · Magnesium ion · metal · chains A

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

Pockets

15 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19430.810.8276NVP
26100.690.7863empty
34710.630.7637empty
42710.610.8025empty
51510.600.8434empty

Interfaces

1 interface between chains.

  • A–B · 2431 Ų buried · 27 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (oxidation).

Compared structures

  • 1VRT · High resolution structures of HIV-1 rt from four rt-inhibitor complexes · the same entry in another collection · chain A against A, TM-score 1.00

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