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TitleDesign of non-covalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides
Journal, issue, pagesJ. Med. Chem., Vol. 45, Page 5321-5329, Year 2002
Publish dateAug 21, 2002 (structure data deposition date)
AuthorsChowdhury, S. / Sivaraman, J. / Wang, J. / Devanathan, G. / Lachance, P. / Qi, H. / Menard, R. / Lefebvre, J. / Konishi, Y. / Cygler, M. ...Chowdhury, S. / Sivaraman, J. / Wang, J. / Devanathan, G. / Lachance, P. / Qi, H. / Menard, R. / Lefebvre, J. / Konishi, Y. / Cygler, M. / Sulea, T. / Purisima, E.O.
External linksJ. Med. Chem. / PubMed:12431059
MethodsX-ray diffraction
Resolution1.9 Å
Structure data

PDB-1mhw:
Design of non-covalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / CATHEPSIN L / CYSTEINE PROTEASE / HYDROLASE-HYDROLASE INHIBITOR COMPLEX

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