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Crystal structure of HIV-1 reverse transcriptase in complex with (E)- 4-(3-(2-cyanovinyl)-5-fluorophenoxy)-3-(2-(2,4-dioxo-3,4- dihydropyrimidin-1(2H)-YL)ETHOXY)PHENYL sulfurofluoridate (JLJ710)

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

PDB
7KRF
Type
protein
Length
957 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
2.7.7.49, 2.7.7.7, 3.1.26.13
UniProt
P03366
Ligands
X2G
Pockets
14 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 34% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHIV-1 reverse transcriptase, P66 subunit (EC 2.7.7.49, 2.7.7.7, 3.1.26.13)protein54832% helix, 24% strandP03366
BHIV-1 reverse transcriptase, P51 subunitprotein40936% helix, 18% strandP03366

Ligands and binding sites

  • X2G · 4-{3-[(E)-2-cyanoethenyl]-5-fluorophenoxy}-3-[2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)ethoxy]phenyl sulfurofluoridate · ligand · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17990.730.7866empty
22920.730.8535X2G
32840.660.8233empty
42640.660.8235empty
53000.640.8151empty

Interfaces

1 interface between chains.

  • A–B · 2551 Ų buried · 19 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 7KRF · Crystal Structure of HIV-1 Reverse Transcriptase in Complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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