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Structure paper

TitleMolecular basis of HIV-1 protease drug resistance: structural analysis of mutant proteases complexed with cyclic urea inhibitors.
Journal, issue, pagesBiochemistry, Vol. 36, Page 1573-1580, Year 1997
Publish dateApr 11, 1997 (structure data deposition date)
AuthorsAla, P.J. / Huston, E.E. / Klabe, R.M. / McCabe, D.D. / Duke, J.L. / Rizzo, C.J. / Korant, B.D. / DeLoskey, R.J. / Lam, P.Y. / Hodge, C.N. / Chang, C.H.
External linksBiochemistry / PubMed:9048541
MethodsX-ray diffraction
Resolution1.9 Å
Structure data

PDB-1mer:
HIV-1 MUTANT (I84V) PROTEASE COMPLEXED WITH DMP450
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

PDB-1mes:
HIV-1 MUTANT (I84V) PROTEASE COMPLEXED WITH DMP323
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

PDB-1met:
HIV-1 MUTANT (V82F) PROTEASE COMPLEXED WITH DMP323
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

PDB-1meu:
HIV-1 MUTANT (V82F, I84V) PROTEASE COMPLEXED WITH DMP323
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-DMQ:
[4-R-(-4-ALPHA,5-ALPHA,6-BETA,7-BETA)]-HEXAHYDRO-5,6-BIS(HYDROXY)-1,3-BIS([(3-AMINO)PHENYL]METHYL)-4,7-BIS(PHENYLMETHYL)-2H-1,3-DIAZEPINONE

ChemComp-DMP:
[4-R-(-4-ALPHA,5-ALPHA,6-BETA,7-BETA)]-HEXAHYDRO-5,6-BIS(HYDROXY)-[1,3-BIS([4-HYDROXYMETHYL-PHENYL]METHYL)-4,7-BIS(PHEN

Source
  • human immunodeficiency virus 1
KeywordsASPARTYL PROTEASE / HYDROLASE / ACID PROTEINASE

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