Zobrazeno 1 - 6
of 6
pro vyhledávání: '"J L Klaus"'
Publikováno v:
Antimicrobial Agents and Chemotherapy. 40:1600-1603
We evaluated the antimalarial effects of vinyl sulfone cysteine proteinase inhibitors. A number of vinyl sulfones strongly inhibited falcipain, a Plasmodium falciparum cysteine proteinase that is a critical hemoglobinase. In studies of cultured paras
Autor:
Bradley A. Katz, Mary E. McGrath, F. R. Mistry, C. J. Linnevers, M. G. Barnes, Randall Armstrong, Dieter Brömme, James T. Palmer, J L Klaus
Publikováno v:
Protein Science. 6:919-921
Cathepsin K is a cysteine protease of the papain family, which is predominantly expressed in osteoclasts, and is regarded as a key protease in bone remodeling. To facilitate structural studies of the protein, the wild-type sequence of the protease ha
Autor:
S L, Biroc, S, Gay, K, Hummel, C, Magill, J T, Palmer, D R, Spencer, S, Sa, J L, Klaus, B A, Michel, D, Rasnick, R E, Gay
Publikováno v:
Arthritis and rheumatism. 44(3)
Cysteine proteases are postulated to play a role in tissue destruction in the joints of animals with arthritis. The purpose of the present study was to confirm the concept that cysteine proteases are enzymes involved in the pathology of rheumatoid ar
Autor:
K I, Hulkower, C C, Butler, B E, Linebaugh, J L, Klaus, D, Keppler, V L, Giranda, B F, Sloane
Publikováno v:
European journal of biochemistry. 267(13)
Cathepsin B and in particular cell-surface and secreted cathepsin B has been implicated in the invasive and metastatic phenotype of numerous types of cancer. We describe here a method to easily survey cancer cell lines for cathepsin B activity using
Autor:
C J, Linnevers, M E, McGrath, R, Armstrong, F R, Mistry, M G, Barnes, J L, Klaus, J T, Palmer, B A, Katz, D, Brömme
Publikováno v:
Protein science : a publication of the Protein Society. 6(4)
Cathepsin K is a cysteine protease of the papain family, which is predominantly expressed in osteoclasts, and is regarded as a key protease in bone remodeling. To facilitate structural studies of the protein, the wild-type sequence of the protease ha
Peptidyl vinyl sulphones are a novel class of extremely potent and specific cysteine protease inhibitors. They are highly active against the therapeutically important cathepsins O2, S and L. The highest kinact/Ki values exceed 107 M-1·s-1 for cathep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8320fa9acb1ce914d34fa5e791ae114b
https://europepmc.org/articles/PMC1217200/
https://europepmc.org/articles/PMC1217200/