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TitleDesign and Structure-Activity Relationships of Novel Inhibitors of Human Rhinovirus 3C Protease.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 26, Page 3248-, Year 2016
Publish dateFeb 24, 2016 (structure data deposition date)
AuthorsKawatkar, S.P. / Gagnon, M. / Hoesch, V. / Tiong-Yip, C. / Johnson, K. / Ek, M. / Nilsson, E. / Lister, T. / Olsson, L. / Patel, J. / Yu, Q.
External linksBioorg. Med. Chem. Lett. / PubMed:27265257
MethodsX-ray diffraction
Resolution1.45 - 1.7 Å
Structure data

PDB-5fx5:
Novel inhibitors of human rhinovirus 3C protease
Method: X-RAY DIFFRACTION / Resolution: 1.7 Å

PDB-5fx6:
Novel inhibitors of human rhinovirus 3C protease
Method: X-RAY DIFFRACTION / Resolution: 1.45 Å

Chemicals

ChemComp-GOL:
GLYCEROL

ChemComp-PG4:
TETRAETHYLENE GLYCOL / precipitant*YM

ChemComp-PGE:
TRIETHYLENE GLYCOL

ChemComp-HOV:
ethyl (4R)-4-[[(2S,3R)-1-[(2S)-3-methyl-2-[(5-methyl-1,2-oxazol-3-yl)carbonylamino]butanoyl]-3-phenyl-pyrrolidin-2-yl]carbonylamino]-5-[(3S)-2-oxidanylidenepyrrolidin-3-yl]pentanoate

ChemComp-HOH:
WATER

ChemComp-6OY:
ethyl (4R)-4-[[(2S,4S)-1-[(2S)-3-methyl-2-[(5-methyl-1,2-oxazol-3-yl)carbonylamino]butanoyl]-4-phenyl-pyrrolidin-2-yl]carbonylamino]-5-[(3S)-2-oxidanylidenepyrrolidin-3-yl]pentanoate

Source
  • human rhinovirus 2
KeywordsTRANSFERASE

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