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Structure paper

TitleThe crystallographic structure of the protease from human immunodeficiency virus type 2 with two synthetic peptidic transition state analog inhibitors.
Journal, issue, pagesJ. Biol. Chem., Vol. 268, Page 13103-13109, Year 1993
Publish dateMar 18, 1993 (structure data deposition date)
AuthorsMulichak, A.M. / Hui, J.O. / Tomasselli, A.G. / Heinrikson, R.L. / Curry, K.A. / Tomich, C.S. / Thaisrivongs, S. / Sawyer, T.K. / Watenpaugh, K.D.
External linksPubMed:8514751
MethodsX-ray diffraction
Resolution2.5 - 2.6 Å
Structure data

PDB-1ivp:
THE CRYSTALLOGRAPHIC STRUCTURE OF THE PROTEASE FROM HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 WITH TWO SYNTHETIC PEPTIDIC TRANSITION STATE ANALOG INHIBITORS
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

PDB-1ivq:
THE CRYSTALLOGRAPHIC STRUCTURE OF THE PROTEASE FROM HUMAN IMMUNODEFICIENCY VIRUS TYPE 2 WITH TWO SYNTHETIC PEPTIDIC TRANSITION STATE ANALOG INHIBITORS
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

Chemicals

ChemComp-1ZK:
4-[(2R)-3-{[(1S,2S,3R,4S)-1-(cyclohexylmethyl)-2,3-dihydroxy-5-methyl-4-({(1S,2R)-2-methyl-1-[(pyridin-2-ylmethyl)carba

ChemComp-HOH:
WATER

ChemComp-0PX:
N~1~-{(1S,2S,4S)-1-(cyclohexylmethyl)-4-[(2,2-dimethylpropyl)carbamoyl]-2-hydroxy-5-methylhexyl}-N~2~-(quinolin-2-ylcar

Source
  • human immunodeficiency virus 2
KeywordsHYDROLASE/HYDROLASE INHIBITOR / ACID PROTEINASE / HYDROLASE-HYDROLASE INHIBITOR complex

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