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Crystal structure of HIV-1 reverse transcriptase (K101P) variant in complex with 8-(2-(2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl) ETHOXY)PHENOXY)INDOLIZINE-2-carbonitrile (JLJ555), a non-nucleoside inhibitor

Analyse Crystal structure of HIV-1 reverse transcriptase (K101P) variant in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5C42
Type
protein
Length
968 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HIV-1 reverse transcriptase, P66 subunit; HIV-1 reverse transcriptase, P51 subunit
EC
3.4.23.16, 2.7.7.49, 2.7.7.7, 3.1.26.13, 3.1.13.2
UniProt
P03366
Ligands
29T
Pockets
19 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 31% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHIV-1 reverse transcriptase, P66 subunit (EC 3.4.23.16, 2.7.7.49, 2.7.7.7, 3.1.26.13, 3.1.13.2)protein54430% helix, 23% strandP03366
BHIV-1 reverse transcriptase, P51 subunit (EC 3.4.23.16, 2.7.7.49, 2.7.7.7, 3.1.26.13, 3.1.13.2)protein42432% helix, 17% strandP03366

Ligands and binding sites

  • 29T · 8-{2-[2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)ethoxy]phenoxy}indolizine-2-carbonitrile · ligand · chains A

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

Pockets

19 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12870.760.884029T
27580.740.7963empty
38130.730.7863empty
43150.690.8337empty
52870.650.8232empty

Interfaces

1 interface between chains.

  • A–B · 2534 Ų buried · 20 hydrogen bonds · protein-protein

Compared structures

  • 5C42 · Crystal Structure of HIV-1 Reverse Transcriptase (K101P) Variant in Complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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