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Structure of HIV-1 reverse transcriptase in a complex with the nonnucleoside inhibitor alpha-apa R 95845 at 2.8 ångströms resolution

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

PDB
1HNI
Type
protein
Length
985 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HIV-1 reverse transcriptase (subunit P66); HIV-1 reverse transcriptase (subunit P51)
EC
2.7.7.49
UniProt
P03366, P03367
Ligands
AAA
Pockets
14 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHIV-1 reverse transcriptase (subunit P66) (EC 2.7.7.49)protein55831% helix, 20% strandP03366
BHIV-1 reverse transcriptase (subunit P51) (EC 2.7.7.49)protein42734% helix, 17% strandP03367

Ligands and binding sites

  • AAA · (2-acetyl-5-methylanilino)(2,6-dibromophenyl)acetamide · 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, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19600.780.8064empty
25820.750.8259AAA
35100.730.8149empty
45570.680.7851empty
52920.670.8239empty

Interfaces

1 interface between chains.

  • A–B · 2513 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 1HNI · Structure of HIV-1 reverse transcriptase in a complex with the nonnucleoside inhibitor… · the same entry in another collection · chain A against A, TM-score 1.00

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