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TitleDesign of selective Cathepsin inhibitors
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 19, Page 4622-4625, Year 2009
Publish dateJun 18, 2009 (structure data deposition date)
AuthorsBethel, P.A. / Gerhardt, S. / Jones, E.V. / Kenny, P.W. / Karoutchi, G.I. / Morley, A.D. / Oldham, K. / Rankine, N. / Augustin, M. / Krapp, S. ...Bethel, P.A. / Gerhardt, S. / Jones, E.V. / Kenny, P.W. / Karoutchi, G.I. / Morley, A.D. / Oldham, K. / Rankine, N. / Augustin, M. / Krapp, S. / Simader, H. / Steinbacher, S.
External linksBioorg. Med. Chem. Lett. / PubMed:19616430
MethodsX-ray diffraction
Resolution2.33 Å
Structure data

PDB-3hwn:
CATHEPSIN L with AZ13010160
Method: X-RAY DIFFRACTION / Resolution: 2.33 Å

Chemicals

ChemComp-BD3:
Nalpha-[(3-tert-butyl-1-methyl-1H-pyrazol-5-yl)carbonyl]-N-[(2E)-2-iminoethyl]-3-{5-[(Z)-iminomethyl]-1,3,4-oxadiazol-2-yl}-L-phenylalaninamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE / Cathepsin L / Drug Design / Disulfide bond / Glycoprotein / Lysosome / Protease / Thiol protease / Zymogen

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