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1 f death diverge at the level of the cysteine aspartase.
2 inate lyase, delta-crystallin, fumarase, and aspartase.
3 ytic cleavage by the endopeptidase threonine aspartase 1 (taspase1); however, the biological signific
4 m in the apoptotic pathway compared with the aspartase activation.
5                                         Mean aspartase aminotransferase increased from 23 (baseline)
6 tenuated, whereas an SR-11 DeltaaspA mutant (aspartase) and an SR-11 DeltafrdABCD mutant (fumarate re
7                                           An aspartase (aspA) mutant (unable to utilize any amino aci
8 itor, blocked the activity/activation of the aspartase at concentrations about one order of magnitude
9 eviously that general inhibitors of cysteine aspartases block apoptosis of PC12 cells and sympathetic
10 a caspase recruitment domain (ASC), cysteine aspartase (caspase)-1, and interleukin (IL)-1beta from i
11                       Activation of cysteine aspartases (caspases) seems to be a required element of
12      In addition to the previously described aspartase-cleavable biosensors, we report development of
13 ed their responses to inhibitors of cysteine aspartases, elements of apoptotic pathways.
14       We find additionally that the cysteine aspartase family protease inhibitor zVAD-fmk inhibits ap
15 mediated by distinct members of the cysteine aspartase family.
16 mology comparisons with other members of the aspartase-fumarase enzyme family, and the necessity for
17 emonstrate reactivities for members of large aspartase/fumarase and pyridoxal 5'-phosphate-dependent
18                           The active site of aspartase has been located in a region that contains sid
19 her, our data highlight the dual function of aspartase in C. jejuni and suggest a role during growth
20 In living cells, zVAD-FMK, a pseudosubstrate aspartase inhibitor, blocked the activity/activation of
21                    In contrast, the cysteine aspartase inhibitory peptide zVAD-fmk conferred protecti
22  raising the possibility that the CPP32-like aspartase is not the main death effector in this model.
23 e that diminished expression of the cysteine aspartase Nedd2 in PC12 cells and sympathetic neurons in
24 enzyme (ICE) and a related group of cysteine aspartases of the ICE/ced-3 family inhibit cell death in
25  and BAF, two peptide inhibitors of cysteine aspartases, protected neurons in all three death paradig
26                                              Aspartase was shown by activity and proteomic analyses t