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Crystal structure of human immunodeficiency virus type 1 reverse transcriptase (rt) in complex with janssen-R100943

Analyse Crystal structure of human immunodeficiency virus type 1 reverse transcriptase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1S6P
Type
protein
Length
979 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.9
Source
Human immunodeficiency virus 1
Molecule
POL polyprotein [Contains: Reverse transcriptase]
EC
2.7.7.49
UniProt
P03366
Ligands
IET, MG
Pockets
15 · best druggability 0.80

Structure

x-ray diffraction · resolution 2.9 · 2 distinct chains · 27% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APOL polyprotein [Contains: Reverse transcriptase] (EC 2.7.7.49)protein55228% helix, 21% strandP03366
BPOL polyprotein [Contains: Reverse transcriptase] (EC 2.7.7.49)protein42727% helix, 15% strandP03366

Ligands and binding sites

  • IET · 1-(4-cyano-phenyl)-3-[2-(2,6-dichloro-phenyl)-1-imino-ethyl]-thiourea · ligand · chains A, B
  • 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, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19480.800.8283IET
28750.750.7980empty
36710.710.7857empty
43110.670.8241empty
52740.670.8342empty

Interfaces

1 interface between chains.

  • A–B · 2625 Ų buried · 30 hydrogen bonds · protein-protein

Compared structures

  • 1S6P · Crystal structure of human immunodeficiency virus type 1 reverse transcriptase (rt) in… · the same entry in another collection · chain A against A, TM-score 1.00

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