نتایج جستجو برای: cysteine proteinase

تعداد نتایج: 44460  

Journal: :Molecules 2008
Marie-Adrienne Dude Ulrich Kaeppler Monika Herb Markus Schiller Franziska Schulz Birgit Vedder Saskia Heppner Gabriele Pradel Jiri Gut Philip J Rosenthal Tanja Schirmeister Matthias Leippe Christoph Gelhaus

A series of etacrynic acid derivatives was synthesized and screened for their in vitro activity against Plasmodium falciparum, as well as their activity against recombinantly expressed falcipain-2 and -3. The two most active compounds of the series displayed IC(50) values of 9.0 and 18.8 microM against Plasmodia.

Journal: :The Journal of clinical investigation 1984
H A Chapman O L Stone

Elastin is an extracellular matrix protein critical to the normal structure and function of human lung. Recently reported data indicate that live human alveolar macrophages can degrade purified elastin in vitro. In this study, we directly compared the elastolytic activity of alveolar macrophages with that of human neutrophils. In the absence of proteinase inhibitors, human neutrophils degrade m...

Journal: :The Biochemical journal 1986
R A McKee S Adams J A Matthews C J Smith H Smith

Two cDNA clones for plant cysteine proteinases have been isolated from a Carica papaya (paw-paw, papaya) leaf tissue cDNA library by using a mixture of 16 synthetic oligodeoxyribonucleotides as a hybridization probe. The inserted regions are 311 and 440 base-pairs in length and have the potential to encode a region corresponding to the C-terminal region of two proteins which are homologous with...

Journal: :The Biochemical journal 1997
A Albeck S Kliper

Peptidyl epoxides are time- and concentration-dependent selective cysteine protease inhibitors. The lack of recovery of enzymic activity and the retention of 1 molar equivalent of radioactive inhibitor associated with the enzyme on dialysis, shown in this study, indicate that they form a covalent irreversible equimolar complex with the enzyme. It is also shown that the peptidyl epoxide inhibito...

Journal: :Biochemistry 2003
Grzegorz Dubin Marcin Krajewski Grzegorz Popowicz Justyna Stec-Niemczyk Matthias Bochtler Jan Potempa Adam Dubin Tad A Holak

A series of secreted proteases are included among the virulence factors documented for Staphylococcus aureus. In light of increasing antibiotic resistance of this dangerous human pathogen, these proteases are considered as suitable targets for the development of novel therapeutic strategies. The recent discovery of staphostatins, endogenous, highly specific, staphylococcal cysteine protease inh...

Journal: :Organic & biomolecular chemistry 2011
Asish K Bhattacharya Kalpeshkumar C Rana Dnyaneshwar S Raut Vaibhav P Mhaindarkar Mohamad I Khan

A novel one-pot route for the synthesis of benzodiazepinyl phosphonates (BDPs) has been achieved. FeCl(3) efficiently catalyzed four-component condensation of diamines, acetone and phosphites in the presence of molecular sieves to furnish BDPs as novel chemical entities with good yield. The synthesized BDPs have shown significant protease inhibition activity against clostripain, a disease model...

Journal: :Cell 1997
Wendy Ward Lilia Alvarado Neil D Rawlings Juan C Engel Christopher Franklin James H McKerrow

Protozoan parasites of the genus Giardia are one of the earliest lineages of eukaryotic cells. To initiate infection, trophozoites emerge from a cyst in the host. Excystation is blocked by specific cysteine protease inhibitors. Using a biotinylated inhibitor, the target protease was identified and its corresponding gene cloned. The protease was localized to vesicles that release their contents ...

Journal: :The Plant cell 1999
M Solomon B Belenghi M Delledonne E Menachem A Levine

Programmed cell death (PCD) is a process by which cells in many organisms die. The basic morphological and biochemical features of PCD are conserved between the animal and plant kingdoms. Cysteine proteases have emerged as key enzymes in the regulation of animal PCD. Here, we show that in soybean cells, PCD-activating oxidative stress induced a set of cysteine proteases. The activation of one o...

2002
Terence A. Walsh

The protein crystals found in potato (Solanum tuberosum 1.) tuber cells consist of a single 85-kD polypeptide. This polypeptide i s an inhibitor of papain and other cysteine proteinases and i s capable of binding several proteinase molecules simultaneously (P. Rodis, J.E. Hoff [1984] Plant Physiol 7 4 907-911). We have characterized this unusual inhibitor in more detail. Titrations of papain ac...

Journal: :Plant physiology 1993
T A Walsh J A Strickland

The protein crystals found in potato (Solanum tuberosum L.) tuber cells consist of a single 85-kD polypeptide. This polypeptide is an inhibitor of papain and other cysteine proteinases and is capable of binding several proteinase molecules simultaneously (P. Rodis, J.E. Hoff [1984] Plant Physiol 74: 907-911). We have characterized this unusual inhibitor in more detail. Titrations of papain acti...

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