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1  more potent and more specific inhibitors of S-adenosylmethionine decarboxylase.
2 of the decarboxylation reaction catalyzed by S-adenosylmethionine decarboxylase.
3 f enzyme alphabeta dimer than with wild-type S-adenosylmethionine decarboxylase.
4 ng stems from mTORC1-dependent regulation of S-adenosylmethionine decarboxylase 1 (AMD1) stability.
5 back by polyamines increased the activity of S-adenosylmethionine decarboxylase 1 (AMD1), leading to
6 tory increase in ornithine decarboxylase and S-adenosylmethionine decarboxylase activities.
7 26 S proteasome caused substantial losses of S-adenosylmethionine decarboxylase activity despite accu
8 ogues diminished ornithine decarboxylase and S-adenosylmethionine decarboxylase activity.
9 otic genes encoding spermidine biosynthesis: S-adenosylmethionine decarboxylase (AdoMetDC) and spermi
10                                              S-adenosylmethionine decarboxylase (AdoMetDC) catalyzes
11                                              S-adenosylmethionine decarboxylase (AdoMetDC) catalyzes
12                            Trypanosoma cruzi S-adenosylmethionine decarboxylase (AdoMetDC) catalyzes
13 lnorspermine [DENSPM]) at 1 microM; however, S-adenosylmethionine decarboxylase (AdoMetDC) depletion
14           The polyamine biosynthetic enzyme, S-adenosylmethionine decarboxylase (ADOMETDC) has been a
15 nt with DFMO in combination with SAM486A, an S-adenosylmethionine decarboxylase (AdoMetDC) inhibitor,
16                                              S-adenosylmethionine decarboxylase (AdoMetDC) is a criti
17                                              S-adenosylmethionine decarboxylase (AdoMetDC) is a criti
18                                              S-Adenosylmethionine decarboxylase (AdoMetDC) is a key e
19                                              S-Adenosylmethionine decarboxylase (AdoMetDC) is a key e
20                                              S-Adenosylmethionine decarboxylase (AdoMetDC) is a pyruv
21                                              S-Adenosylmethionine decarboxylase (AdoMetDC) is a pyruv
22                                              S-Adenosylmethionine decarboxylase (AdoMetDC) is a pyruv
23                                              S-Adenosylmethionine decarboxylase (AdoMetDC) is a pyruv
24                                              S-Adenosylmethionine decarboxylase (AdoMetDC) is a pyruv
25                                              S-Adenosylmethionine decarboxylase (AdoMetDC) is synthes
26 the 5' leader of the mammalian mRNA encoding S-adenosylmethionine decarboxylase (AdoMetDC) serves as
27 ssing and decarboxylation reactions of human S-adenosylmethionine decarboxylase (AdoMetDC), a critica
28                                              S-adenosylmethionine decarboxylase (AdoMetDC), a key enz
29     Previously we showed that trypanosomatid S-adenosylmethionine decarboxylase (AdoMetDC), a key enz
30                                 Synthesis of S-adenosylmethionine decarboxylase (AdoMetDC), a key reg
31 hibitor of the polyamine biosynthetic enzyme S-adenosylmethionine decarboxylase (AdoMetDC), is presen
32                       Instead trypanosomatid S-adenosylmethionine decarboxylase (AdoMetDC), which cat
33        Instead they have two paralogs of the S-adenosylmethionine decarboxylase (AdoMetDC).
34 ne fusions of polyamine biosynthetic enzymes S-adenosylmethionine decarboxylase (AdoMetDC, speD) and
35                                              S-adenosylmethionine decarboxylase (AdoMetDC/SpeD) is a
36  and arginine decarboxylase (ADC), arginase, S-adenosylmethionine decarboxylase (AdoMetDC/speD), sper
37 eport X-ray structures of Trypanosoma brucei S-adenosylmethionine decarboxylase alone and in function
38 n of histone genes, selenoprotein genes, and S-adenosylmethionine decarboxylase (AMD1).
39 putrescine amidohydrolase in archaea, and of S-adenosylmethionine decarboxylase and ornithine decarbo
40 permidine from putrescine by the key enzymes S-adenosylmethionine decarboxylase and spermidine syntha
41 erimental frameshift frequencies measured in S-adenosylmethionine-decarboxylase and antizyme mutants,
42 ynthetic enzymes ornithine decarboxylase and S-adenosylmethionine decarboxylase, and upregulates sper
43 carboxylase activity despite accumulation of S-adenosylmethionine decarboxylase antigen.
44 n in COS-7 cells prevents the degradation of S-adenosylmethionine decarboxylase antigen; however, eve
45 because of a deletion in the gene coding for S-adenosylmethionine decarboxylase are very sensitive to
46                           In contrast, plant S-adenosylmethionine decarboxylases are fully active in
47 samination accelerates normal degradation of S-adenosylmethionine decarboxylase, as the rate of degra
48                                              S-Adenosylmethionine decarboxylase belongs to a small cl
49 ocess that is accelerated by inactivation of S-adenosylmethionine decarboxylase by substrate-mediated
50         We have determined the structures of S-adenosylmethionine decarboxylase complexed with the co
51  a deletion-insertion in the gene coding for S-adenosylmethionine decarboxylase (Deltaspe2) have an a
52 ethyltetrahydrofolate:Hcy methyltransferase, S-adenosylmethionine decarboxylase, DNA methyltransferas
53                                              S-Adenosylmethionine decarboxylase from Escherichia coli
54      We have determined the structure of the S-adenosylmethionine decarboxylase from potato, Solanum
55 strated by isolation of His-tagged AdoMetDC (S-adenosylmethionine decarboxylase) from COS-7 cells co-
56                         We expressed a yeast S-adenosylmethionine decarboxylase gene (ySAMdc; Spe2) f
57                                              S-Adenosylmethionine decarboxylase has a four-layer alph
58                                              S-Adenosylmethionine decarboxylase has been implicated i
59 he activities of ornithine decarboxylase and S-adenosylmethionine decarboxylase in a similar fashion.
60 in the constitutively high activity of plant S-adenosylmethionine decarboxylases in the absence of pu
61 tain the optimal structural requirements for S-adenosylmethionine decarboxylase inhibition and potent
62 re provide a framework for interpretation of S-adenosylmethionine decarboxylase inhibition data and s
63 hibitor alpha-difluoromethylornithine or the S-adenosylmethionine decarboxylase inhibitor MDL-73811 l
64 razone (MGBG), a polyamine analog and potent S-adenosylmethionine decarboxylase inhibitor, decreases
65 en reading frame (uORF) in the mRNA encoding S-adenosylmethionine decarboxylase is a cis-acting eleme
66 en reading frame (uORF) in the mRNA encoding S-adenosylmethionine decarboxylase is a polyamine-respon
67                                              S-Adenosylmethionine decarboxylase is a pyruvate-depende
68                                  In mammals, S-adenosylmethionine decarboxylase is active as a dimer
69                            Ubiquitination of S-adenosylmethionine decarboxylase is demonstrated by is
70                                        Human S-adenosylmethionine decarboxylase is synthesized as a p
71                     Here we demonstrate that S-adenosylmethionine decarboxylase is ubiquitinated and
72 ypanosomatid spermidine biosynthetic enzyme, S-adenosylmethionine decarboxylase, is regulated by hete
73    The availability of the recombinant H243A S-adenosylmethionine decarboxylase proenzyme provides a
74 '-deoxyadenosine (MDL73811), an inhibitor of S-adenosylmethionine decarboxylase, resulted in increase
75                        In the present study, S-adenosylmethionine decarboxylase (SAMDC), a key gene i
76 ynthesis, ornithine decarboxylase (ODC), and S-adenosylmethionine decarboxylase (SAMdc), were measure
77 Syn was horizontally acquired as a bacterial S-adenosylmethionine decarboxylase-SpmSyn fusion protein
78 ion levels of ornithine decarboxylase and of S-adenosylmethionine decarboxylase, two essential enzyme
79 irect evidence of peptide synthesis from the S-adenosylmethionine decarboxylase uORF using an in vitr
80                       The short-lived enzyme S-adenosylmethionine decarboxylase uses a covalently bou
81             The catalytic mechanism of human S-adenosylmethionine decarboxylase was investigated via
82               Both wild-type and C82A mutant S-adenosylmethionine decarboxylases were inactivated by