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Structure paper

TitleCrystallographic studies on the binding modes of P2-P3 butanediamide renin inhibitors.
Journal, issue, pagesJ. Biol. Chem., Vol. 270, Page 29520-29524, Year 1995
Publish dateSep 27, 1995 (structure data deposition date)
AuthorsTong, L. / Pav, S. / Lamarre, D. / Simoneau, B. / Lavallee, P. / Jung, G.
External linksJ. Biol. Chem. / PubMed:7493993
MethodsX-ray diffraction
Resolution2.4 - 2.8 Å
Structure data

PDB-1bil:
CRYSTALLOGRAPHIC STUDIES ON THE BINDING MODES OF P2-P3 BUTANEDIAMIDE RENIN INHIBITORS
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

PDB-1bim:
CRYSTALLOGRAPHIC STUDIES ON THE BINDING MODES OF P2-P3 BUTANEDIAMIDE RENIN INHIBITORS
Method: X-RAY DIFFRACTION / Resolution: 2.8 Å

Chemicals

ChemComp-0IU:
(2S)-2-[(2-amino-1,3-thiazol-4-yl)methyl]-N~1~-[(1S,2R,3R)-1-(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl]-N~4~-[2-(d

ChemComp-HOH:
WATER

ChemComp-0QB:
(2S)-2-[(2-amino-1,3-thiazol-4-yl)methyl]-N~1~-{(1S,2S)-1-(cyclohexylmethyl)-2-hydroxy-2-[(3R)-1,5,5-trimethyl-2-oxopyrrolidin-3-yl]ethyl}-N~4~-[2-(dimethylamino)-2-oxoethyl]-N~4~-[(1S)-1-phenylethyl]butanediamide

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / ASPARTIC PROTEINASE / Aspartyl protease / Cleavage on pair of basic residues / Disease mutation / Disulfide bond / Glycoprotein / Hydrolase / Membrane / Protease / Secreted / Zymogen / HYDROLASE-HYDROLASE INHIBITOR complex

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