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1 a Lys-50 mutant that blocks modification by deoxyhypusine.
2 pusine or selectively to hypusine but not to deoxyhypusine.
3 educed enzyme intermediate was identified as deoxyhypusine and was shown to occur at a single locus.
4 ural (2S,9R)-hypusine, (2S,9S)-hypusine, and deoxyhypusine- and hypusine-containing peptides are desc
6 rain with deletion of YJR070C contained only deoxyhypusine but no hypusine, indicating that YJR070C w
7 hypusine synthase catalyzes the formation of deoxyhypusine by conjugation of the butylamine moiety of
10 maleimide conjugates, as well as against the deoxyhypusine-containing and lysine-containing hexapepti
11 al gel analyses revealed the accumulation of deoxyhypusine-containing eIF5A [eIF5A(Dhp)] and a reduct
12 due in the eIF5A precursor protein to form a deoxyhypusine-containing eIF5A intermediate, eIF5A(Dhp).
13 isplayed a strong preference for binding the deoxyhypusine-containing form of eIF5A, over the eIF5A p
15 The availability of synthetic hypusine and deoxyhypusine has made it possible to develop analytical
22 sttranslational modification event requiring deoxyhypusine hydroxylase (DOHH), an enzyme that can be
23 ow that PCBP1 and PCBP2 also deliver iron to deoxyhypusine hydroxylase (DOHH), the dinuclear iron enz
24 ng enzymes-deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxylase (DOHH)-and hypusinated eukaryo
32 modifying enzymes deoxyhypusine synthase and deoxyhypusine hydroxylase as well as for the cancer-rela
33 s depletion of deoxyhypusine synthase and/or deoxyhypusine hydroxylase causes lethality in adult mice
37 on multiple cell processes, suggesting that deoxyhypusine/hypusine biosynthesis could be a promising
38 tic NOD mice that received injections of the deoxyhypusine inhibitor N1-guanyl-1,7-diaminoheptane (GC
40 novel cofactor called trypanothione and for deoxyhypusine modification of eukaryotic translation ini
42 synthetic methods which allow access to (2S)-deoxyhypusine, natural (2S,9R)-hypusine, (2S,9S)-hypusin
44 The antibodies bind to both hypusine and deoxyhypusine or selectively to hypusine but not to deox
45 thesis, as donor substrates for synthesis of deoxyhypusine (or its analog), and for synthesis of homo
46 e methods involve both the construction of a deoxyhypusine reagent in which the alpha-nitrogen protec
49 at it can carry out the hydroxylation of the deoxyhypusine residue present in the elF5A substrate.
50 lation at the 4-aminobutyl side chain of the deoxyhypusine residue prevents deoxyhypusine synthase-me
53 iolabeled in the 4-aminobutyl portion of its deoxyhypusine residue, was incubated with human deoxyhyp
54 A binding in which the amino group(s) of the deoxyhypusine side chain of the substrate is primarily a
55 is a two-step reaction involving the enzymes deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
57 two sequential enzymatic steps catalyzed by deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
58 eIF5A post-translationally via two enzymes, deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
59 s and Main Results: Hypusine forming enzymes-deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
60 sination, which is catalyzed by two enzymes, deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
61 s catalyzed by two enzymatic steps involving deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxyl
62 nd mouse models with inducible knockdowns of deoxyhypusine synthase (DHPS) and eIF5A to investigate t
67 In-vivo inhibition of elF5A hypusination by deoxyhypusine synthase (DHS) inhibitor "GC7" was studied
71 pusine formation by a selective inhibitor of deoxyhypusine synthase and by its depletion with RNA int
72 two sequential enzymatic steps catalyzed by deoxyhypusine synthase and deoxyhypusine hydroxylase (DO
73 se models for the hypusine-modifying enzymes deoxyhypusine synthase and deoxyhypusine hydroxylase as
77 We discovered that homozygous depletion of deoxyhypusine synthase and/or deoxyhypusine hydroxylase
88 SS, we identified sequences encoding HSS and deoxyhypusine synthase from various species of the Convo
89 of transcript levels have shown that HSS and deoxyhypusine synthase have also diverged with respect t
90 s suggest a previously unrecognized role for deoxyhypusine synthase in promoting T cell proliferation
93 Th17, and Treg), but those treated with the deoxyhypusine synthase inhibitor GC7 showed a dose-depen
94 ctive metabolite that functions similarly to deoxyhypusine synthase inhibitors but has other unidenti
100 tion in the single copy gene, yDHS, encoding deoxyhypusine synthase results in the loss of viability
102 of human DOHH along with eIF5A precursor and deoxyhypusine synthase was required for overproduction o
103 erythroid progenitors, by the inhibition of deoxyhypusine synthase, abrogates erythropoiesis but not
104 endently by duplication of the gene encoding deoxyhypusine synthase, an enzyme involved in the posttr
106 ivity, formation of different complexes with deoxyhypusine synthase, and Km values (1.5 +/- 0.2 vs. 8
107 f eukaryotic initiation factor 5A (eIF5A) by deoxyhypusine synthase, employing spermidine as a butyla
108 xyhypusine residue, was incubated with human deoxyhypusine synthase, NAD, and 1,3-diaminopropane, [3H
109 nsion of this prozyme paradigm to the enzyme deoxyhypusine synthase, which is required for spermidine
110 differentiation by providing substrates for deoxyhypusine synthase, which synthesizes the amino acid
111 chain of the deoxyhypusine residue prevents deoxyhypusine synthase-mediated reversal of the modifica
119 t here at 2.2 A a new Form II crystal of the deoxyhypusine synthase:NAD holoenzyme grown at low ionic
120 enzyme-substrate intermediate formation and deoxyhypusine synthesis activity, indicating that Lys329
121 diate and that it is absolutely required for deoxyhypusine synthesis in the eukaryotic translation in
122 rison of spermidine analogs as inhibitors of deoxyhypusine synthesis, as donor substrates for synthes
123 type enzyme) suggesting that in contrast to deoxyhypusine synthesis, spermidine cleavage can occur w
126 reduction of the eIF5A-imine intermediate to deoxyhypusine was reflected by a rapid decrease in the N