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1 ernal through hydrolysis of Q by a dedicated nucleosidase.
2 - and poly-(ADP-ribose) polymerases, and NAD nucleosidase.
3 , or compounds that can be cleaved by AdoHcy nucleosidase.
5 ycolate and 3'-abasic sites, and exhibits 3'-nucleosidase activity indicating it may function as a ge
7 hosphorylation site and resulted in elevated nucleosidase activity, which is a known consequence of g
10 AI-2), produced by the purified enzymes Pfs (nucleosidase) and LuxS (terminal synthase) from S-adenos
12 Interestingly, the inhibitors of MTA/SAH nucleosidase are very effective against the Lyme disease
13 leoside hydrolases is active as a pyrimidine nucleosidase but shows the highest specificity toward th
14 ation of the public protease and the private nucleosidase by QS stabilizes cooperation, and the data
16 s, is first hydrolyzed by recombinant AdoHcy nucleosidase (EC 3.2.2.9) into adenine and S-ribosylhomo
18 tate of Escherichia coli methylthioadenosine nucleosidase (EcMTAN) by transition state analysis and c
19 ioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidase in bacteria has started to be appreciated o
20 dvantage of this assay which includes AdoHcy nucleosidase is the destruction of AdoHcy, thus alleviat
22 employed them to measure methylthioadenosine nucleosidase (MTAN) activity in live Escherichia coli.
23 sphorylase (MTAP) and 5'-methylthioadenosine nucleosidase (MTAN) catalyze the phosphorolysis and hydr
24 Methylthioadenosine/S-adenosylhomocysteine nucleosidase (MTAN) catalyzes reactions linked to polyam
25 '-Methylthioadenosine/S-adenosylhomocysteine nucleosidase (MTAN) catalyzes the hydrolytic cleavage of
27 '-methylthioadenosine/S-adenosylhomocysteine nucleosidase (MTAN) enzyme is a multifunctional enzyme t
29 -methylthioadenosine/ S-adenosylhomocysteine nucleosidase (MTAN) hydrolyzes adenine from its substrat
30 -methylthioadenosine/S-adenosyl-homocysteine nucleosidase (MTAN) hydrolyzes its substrates to form ad
31 hate (ATP) by 5'-methylthio-adenosine/AdoHcy nucleosidase (MTAN), adenine phosphoribosyl transferase
34 of MTA is salvaged by 5'-methylthioadenosine nucleosidase (MTN) in a reaction producing methylthiorib
35 '-methylthioadenosine/S-adenosylhomocysteine nucleosidase (Pfs-2), previously described as Bgp, a gly
36 novel pathway in which NR is degraded by the nucleosidases Pnp1 and Urh1, with a minor role for Meu1,
37 increased up to 2-fold by the addition of a nucleosidase, presumably by degrading the inactive by-pr
38 e identified Arabidopsis methylthioadenosine nucleosidase proteins MTN1 and MTN2 as putative targets
39 for inosine, guanosine, and adenosine in the nucleosidase reaction and 45.6, 35.9, and 12.3 microM fo
42 ese reactions, and are substrates of MTA/SAH nucleosidase, underscoring its importance in a wide arra
43 assay is the destruction of AdoHcy by AdoHcy nucleosidase, which alleviates AdoHcy product feedback i
44 '-methylthioadenosine/S-adenosylhomocysteine nucleosidase, which hydrolyses 5'-methylthioadenosine, t