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Structure paper

TitleStructural basis for drug and substrate specificity exhibited by FIV encoding a chimeric FIV/HIV protease.
Journal, issue, pagesActa Crystallogr. ,Sect. D, Vol. 67, Page 540-548, Year 2011
Publish dateAug 17, 2010 (structure data deposition date)
AuthorsLin, Y.C. / Perryman, A.L. / Olson, A.J. / Torbett, B.E. / Elder, J.H. / Stout, C.D.
External linksActa Crystallogr. ,Sect. D / PubMed:21636894
MethodsX-ray diffraction
Resolution1.7 - 1.8 Å
Structure data

PDB-3ogp:
Crystal Structure of 6s-98S FIV Protease with Darunavir bound
Method: X-RAY DIFFRACTION / Resolution: 1.7 Å

PDB-3ogq:
Crystal Structure of 6s-98S FIV Protease with Lopinavir bound
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

Chemicals

ChemComp-017:
(3R,3AS,6AR)-HEXAHYDROFURO[2,3-B]FURAN-3-YL(1S,2R)-3-[[(4-AMINOPHENYL)SULFONYL](ISOBUTYL)AMINO]-1-BENZYL-2-HYDROXYPROPYLCARBAMATE / medication*YM

ChemComp-DMS:
DIMETHYL SULFOXIDE / DMSO, precipitant*YM

ChemComp-HOH:
WATER

ChemComp-AB1:
N-{1-BENZYL-4-[2-(2,6-DIMETHYL-PHENOXY)-ACETYLAMINO]-3-HYDROXY-5-PHENYL-PENTYL}-3-METHYL-2-(2-OXO-TETRAHYDRO-PYRIMIDIN-1-YL)-BUTYRAMIDE

Source
  • feline immunodeficiency virus
KeywordsHYDROLASE/HYDROLASE INHIBITOR / aspartyl protease / HIV-like FIV chimera / HYDROLASE-HYDROLASE INHIBITOR complex

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