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Structure paper

TitlePotent antiviral HIV-1 protease inhibitor combats highly drug resistant mutant PR20.
Journal, issue, pagesBiochem. Biophys. Res. Commun., Vol. 519, Page 61-66, Year 2019
Publish dateJul 10, 2019 (structure data deposition date)
AuthorsKneller, D.W. / Agniswamy, J. / Ghosh, A.K. / Weber, I.T.
External linksBiochem. Biophys. Res. Commun. / PubMed:31474336
MethodsX-ray diffraction
Resolution1.21 Å
Structure data

PDB-6prf:
HIV-1 Protease multiple drug resistant clinical isolate mutant PR20 with GRL-14213A
Method: X-RAY DIFFRACTION / Resolution: 1.21 Å

Chemicals

ChemComp-Y1:
YTTRIUM ION

ChemComp-7OA:
(3S,3aR,5R,7aS,8S)-hexahydro-4H-3,5-methanofuro[2,3-b]pyran-8-yl [(2S,3R)-4-[{[2-(cyclopropylamino)-1,3-benzothiazol-6-yl]sulfonyl}(2-methylpropyl)amino]-1-(3,5-difluorophenyl)-3-hydroxybutan-2-yl]carbamate

ChemComp-HOH:
WATER

Source
  • human immunodeficiency virus type 1 group m subtype
KeywordsHydrolase/Hydrolase Inhibitor / Protease / Inhibitor / Multiple Mutant / Viral Protein complex / HYDROLASE / Hydrolase-Hydrolase Inhibitor / Hydrolase-Hydrolase Inhibitor complex

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