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Structure paper

TitleSpecificity determinants of human cathepsin s revealed by crystal structures of complexes.
Journal, issue, pagesBiochemistry, Vol. 42, Page 3203-3213, Year 2003
Publish dateJan 20, 2003 (structure data deposition date)
AuthorsPauly, T.A. / Sulea, T. / Ammirati, M. / Sivaraman, J. / Danley, D.E. / Griffor, M.C. / Kamath, A.V. / Wang, I.K. / Laird, E.R. / Seddon, A.P. ...Pauly, T.A. / Sulea, T. / Ammirati, M. / Sivaraman, J. / Danley, D.E. / Griffor, M.C. / Kamath, A.V. / Wang, I.K. / Laird, E.R. / Seddon, A.P. / Menard, R. / Cygler, M. / Rath, V.L.
External linksBiochemistry / PubMed:12641451
MethodsX-ray diffraction
Resolution1.8 - 2 Å
Structure data

PDB-1npz:
Crystal structures of Cathepsin S inhibitor complexes
Method: X-RAY DIFFRACTION / Resolution: 2 Å

PDB-1nqc:
Crystal structures of Cathepsin S inhibitor complexes
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

Chemicals

ChemComp-C1P:
N~2~-(morpholin-4-ylcarbonyl)-N-[(3S)-1-phenyl-5-(phenylsulfonyl)pentan-3-yl]-L-leucinamide

ChemComp-HOH:
WATER

ChemComp-C4P:
N-[(1R)-2-(BENZYLSULFANYL)-1-FORMYLETHYL]-N-(MORPHOLIN-4-YLCARBONYL)-L-PHENYLALANINAMIDE

Source
  • homo sapiens (human)
KeywordsHYDROLASE / Antigen presentation / binding specificity / cysteine proteases / inhibitor complexes / structure-based design / structural plasticity

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