1 We hypothesized that the RdgB protein
is active on 2'-deoxy-N-6-hydroxylaminopurine triphospha
2 double acetylated mannoses, while the RiCE2
is active on 3-O-, 4-O-, and 6-O-acetylations.
3 DinG
is active on 5'-flap structures; however, it is unable t
4 Both epsilonNRA-I and epsilonNRA-II
are active on a heterologous promoter and hence appear t
5 that adopt a common beta-jelly-roll fold and
are active on a range of terrestrial and marine polysacc
6 Such a feedback mechanism is likely to
be active on a within-breath basis to protect upper airw
7 Kinetic analyses demonstrated that PDCR
is active on a broad range of Delta(2), Delta(4)-dienoyl
8 In contrast, although the enzyme
is active on a regressed fork structure, RuvB loading by
9 like, 12-bp promoter core, AATATTAAAGGG, and
is active on a reporter only in butyrate-induced KSHV-in
10 ould explain the observation that the enzyme
is active on a variety of small, acetylated molecules.
11 amygdala neurons showed that this population
was active on a behaviorally relevant timescale and part
12 The enzyme
was active on a variety of aromatic substrates, includin
13 nC. kronotskyensis, when produced inE. coli,
was active on a variety of xylans and beta-glucans.
14 Both enzymes
were active on acetylated substrates, although each show
15 Factor VIII mutants
were active on additional membrane sites and had altered
16 g yeast, the nuclear RNA surveillance system
is active on all pre-mRNA transcripts and modulated by n
17 This enzyme
is active on all recombinant human core histones, but hi
18 ProPLA2
is active on an anionic interface, but at a rate that is
19 Despite their pervasiveness, whether they
are active on any targets has not been systematically ex
20 idence from spacecraft data that the process
is active on asteroid surfaces.
21 To establish whether proteasome inhibitors
are active on B cells, being plasma cell precursors, we
22 rized a glycoside hydrolase 109 (GH109) that
is active on blood type A-antigen, along with a new subf
23 dly expressed in these tissues and that they
are active on both apical and basolateral surfaces.
24 Whereas the bacterial homologs
are active on both DNA and RNA, the mammalian variants o
25 mized this series to potent derivatives that
are active on both human and murine GPBAR1.
26 and are part of a small group of genes that
are active on both sex chromosomes.
27 macrocyclization enzymes have been shown to
be active on both peptide and protein substrates.
28 We show here that RNase BN
is active on both double- and single-stranded RNA but th
29 The enzyme
is active on both seleno-Cys and Cys but has a much high
30 ctive on indole-3-acetic acid (IAA), and one
was active on both IAA and salicylic acid.
31 These results demonstrate that LCOs
are active on Brachypodium roots and stimulate LRF proba
32 The Slx1-Slx4 nuclease
is active on branched DNA substrates, particularly simpl
33 s the MFP2 L-3-hydroxyacyl-CoA dehydrogenase
is active on C6:0, C12:0 and C18:0 substrates.
34 by enzymatic assay, showed that this enzyme
is active on C8:0- to C14:0-coenzyme A with maximal acti
35 In this study, we show that MT-SP1
is active on cancer cells and that its activity may be t
36 rs in making available endocannabinoids that
are active on CB1 receptors in synaptic neurons.
37 specificities revealed that all these LPMOs
are active on cellulose and cello-oligosaccharides, as w
38 Fungal AA9 LPMOs
are active on cellulose, but some members also display a
39 tward shift in the pressure-gating curve and
was active on closed channels.
40 avily sulfated, but specific sulfatases that
are active on colonic mucins have not been identified.
41 (GH26) family are retaining hydrolases that
are active on complex heteromannans and whose genes are
42 Nun
is active on complexes located at any template site test
43 a pathogenicity island 1 (SPI1)-encoded TTSS
is active on contact with host cells, whereas the Salmon
44 Since DinG is DNA damage-inducible and
is active on D-loops and forked structures, which mimic
45 and 3' apurinic/apyrimidinic (AP) lyase that
is active on DNA substrates containing A/G, A/C, or A/8-
46 Dug
was active on duplex oligonucleotides (34-mers) that con
47 Although DDX43
was active on duplex RNA regardless of the orientation o
48 ces in potency were observed, each inhibitor
was active on each cell type and trans infection was sim
49 ic acid, consistent with the fact that GH3.6
was active on each of these auxins.
50 ation of alpha- and beta-chemokines known to
be active on eosinophils and mononuclear cells, includin
51 biochemical assays showed that, while TgALD1
was active on F16BP, TgDPA was inactive on dR5P.
52 Both enzymes
are active on farnesyl- and geranylgeranylcysteine, but
53 an enzyme, A22 resolvase, which is known to
be active on four-stranded DNA junctions (Holliday junct
54 the first time that VapC-1 is an RNase that
is active on free RNA but does not degrade DNA in vitro.
55 We showed that the enzyme
was active on Galalpha1-3Gal but not the blood group B a
56 showing that these plasma protein inhibitors
are active on GAS cells.
57 In addition, trastuzumab-DM1
was active on HER2-overexpressing, trastuzumab-refractor
58 the ribbon isoform of the truncated peptide
is active on heterologously expressed muscle nAChRs, sug
59 The enzymes
are active on histone substrates that have been acetylat
60 fection, supporting the hypothesis that TOP1
is active on HSV-1 genomes during infection.IMPORTANCEHS
61 (Ss)RidA-1
was active on IA derived from nonpolar amino acids and p
62 mplementary insertion mutant U7 was shown to
be active on insertion substrates further mutated to all
63 nds are potent anti-inflammatory agents that
are active on local intravenous as well as oral administ
64 cates of each novel bradykinin were found to
be active on mammalian arterial and small intestinal smo
65 ed for in vivo biological activity, only one
was active on mice but all three had effects on fish.
66 binding proteins and permeases predicted to
be active on milk oligosaccharides.
67 We show that the M. jannaschii enzyme
is active on minihelix substrates over a wide temperatur
68 We found that the nTET and mTET1 enzymes
were active on modified mC residues in single-stranded a
69 All four new enzymes were found to
be active on multiple prenyl-diphosphate substrates with
70 Kallikreins
were active on mutated B(2) receptor missing the 19 N-te
71 id peptide named alpha-conotoxin Lo1a, which
is active on nAChRs.
72 suggests the potential for the enzymes that
are active on NDAT in vitro to act on DAT in vivo and in
73 array of chemically diverse chemoattractants
is active on neutrophils and participates in recruitment
74 moderate strand displacement activity, as it
was active on nicked and gapped templates, and displaced
75 fungus Neurospora crassa that are likely to
be active on novel substrates.
76 In contrast, PRC1
was active on nucleosomal arrays formed with tailless hi
77 The network
is active on one of the two anaphase B spindle-pole bodi
78 to identify additional plant compounds that
are active on other types of TRP channels.
79 It
was active on p-nitrophenyl-alpha-d-xyloside, isoprimeve
80 The enzyme
is active on P3N and other alkyl nitronates, but cannot
81 ydrolyse phosphatidylcholine (PC), only PlcB
is active on phosphatidylethanolamine (PE).
82 rated a humanized M1'-specific antibody that
was active on primary human cells in vivo, as determined
83 udies suggest that recombinant Dot1 proteins
are active on recombinant nucleosomes, free of any modif
84 UT10 have activity toward RG-I, while AtFUT8
was active on RG-II.
85 ditions, and the results show that a monomer
is active on short duplexes yet multiple molecules are n
86 is up-regulated during HMO fermentation and
is active on sialylated lacto-N-tetraose.
87 t of the uracil-excision enzyme or for it to
be active on single-stranded DNA.
88 This nuclease
is active on single- and double-stranded DNA.
89 es with acyl chains of 6-16 carbon atoms and
is active on some, but not all, non-native ACP species t
90 lix is formed, and the transcription process
is active (ON state).
91 DinG
is active on synthetic D-loops and R-loops.
92 Screening of a number of cytokines known to
be active on T cells identified only TGF-beta1 as able t
93 ulatory molecules and of an immunotoxin that
is active on T cells have been particularly important ad
94 All three LPMOs
were active on tamarind xyloglucan and konjac glucomanna
95 development of Notch pathway inhibitors that
are active on target genes containing paired sites.
96 is suggests that only motors of one polarity
are active on the cargo at any instant in time and is no
97 nked trait that is influenced by genes which
are active on the female chromosome.
98 A set of imprinted genes that
are active on the paternal but silenced on the maternal
99 at new U2U pairs often form while both users
are active on the same DWM, suggesting the marketplace m
100 ubset of the mutations present in those that
are active on the single-mutant mFRTs, plus additional m
101 beta-1-3 glucan, because both CelC and LicA
are active on the substrate.
102 d against the coronavirus disease of 2019 to
be active on the United Network for Organ Sharing waitin
103 ly limits Comm activity and prevents it from
being active on the contralateral side of the central ne
104 rominent, only one electron-transfer pathway
is active on the donor side of PSII.
105 ter requires the maternal Wnt pathway, which
is active on the dorsal side of embryos.
106 The data suggest that the Pet toxin
is active on the human intestinal mucosa but that EAEC m
107 S. pombe are conservative, and that the SIN
is active on the new SPB.
108 However, the R1162 MobA
is active on the oriT of pSC101, another naturally occur
109 active centromere on one homolog and D17Z1-B
is active on the other.
110 The major protein kinase that
is active on the p70 S6 kinase hydrophobic regulatory si
111 The P3 promoter that
is active on the plasmid was not utilized at the chromos
112 ic, BMP/ALK2/Smad-mediated signaling pathway
is active on the right side of the Xenopus embryo.
113 The results show that RecG
is active on the substrates in group 1, whereas these ar
114 Unexpectedly, SETD3
was active on the substituted methionine, generating S-m
115 None of the putative OsFUTs
were active on the RG-I and RG-II.
116 ces of magmatism and topographic uplift that
were active on the rifted margins of the North Atlantic
117 A total of 23.3% of patients
were active on the transplant waiting list.
118 ) were inactive on the waitlist, 11,529 (2%)
were active on the waitlist, and 480,517 (85%) had never
119 These enzymes
are active on thioester-containing substrates, specifica
120 Electrophysiologists
are active on Twitter, with modest influence often repre
121 This novel repression domain
was active on two target genes that are normally repress
122 Although streptococcal and Bacillus UGLs
were active on unsaturated heparin disaccharides, those
123 lypharmacology standpoint, Pz-1 was shown to
be active on VEGFR2, which can block the blood supply re
124 Recombinant jojoba FAO and FADH proteins
are active on very-long-chain fatty alcohol and fatty al
125 amma-32P]ATP incorporation assay, the enzyme
is active on wild-type catalytic subunit and on an inact
126 SC) had a major effect on activity: NcLPMO9A
was active on xyloglucan only in the presence of PASC, a