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Structure paper

TitleStructural basis for reversible and irreversible inhibition of human cathepsin L by their respective dipeptidyl glyoxal and diazomethylketone inhibitors.
Journal, issue, pagesJ. Struct. Biol., Vol. 173, Page 14-19, Year 2011
Publish dateAug 14, 2010 (structure data deposition date)
AuthorsShenoy, R.T. / Sivaraman, J.
External linksJ. Struct. Biol. / PubMed:20850545
MethodsX-ray diffraction
Resolution1.761 - 2.2 Å
Structure data

PDB-3of8:
Structural Basis for Reversible and Irreversible Inhibition of Human Cathepsin L by their Respective Dipeptidyl Glyoxal and Diazomethylketone Inhibitors
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

PDB-3of9:
Structural Basis for Irreversible Inhibition of Human Cathepsin L by a Diazomethylketone Inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.761 Å

Chemicals

ChemComp-I0Y:
Nalpha-[(benzyloxy)carbonyl]-N-[(2S)-1-(4-tert-butoxyphenyl)-4-hydroxy-3-oxobutan-2-yl]-L-phenylalaninamide

ChemComp-HOH:
WATER

ChemComp-I0X:
Nalpha-[(benzyloxy)carbonyl]-N-[(1S)-1-(4-tert-butoxybenzyl)-3-diazo-2-oxopropyl]-L-phenylalaninamide

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / HYDROLASE-HYDROLASE INHIBITOR complex

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