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1 -associated complex alpha subunit and a tRNA nucleotidyltransferase.
2 rally requires the action of the enzyme tRNA nucleotidyltransferase.
3 artially compensated for the absence of tRNA nucleotidyltransferase.
4 of 3'-CC forms of the RNAs by CTP, ATP:tRNA nucleotidyltransferase.
5 ndrial, cytosolic, and nuclear ATP(CTP):tRNA nucleotidyltransferase.
6 ally by the CCA-adding enzyme, a specialized nucleotidyltransferase.
7 transferase, and NTSFIII as an A-adding tRNA nucleotidyltransferase.
8 es and is a member of a large superfamily of nucleotidyltransferases.
9 ng that the basic mechanism is found in many nucleotidyltransferases.
10 ar nucleotidyltransferases but also in other nucleotidyltransferases.
11 cyclases and a family of DNA polymerases and nucleotidyltransferases.
12 of class I enzymes within the superfamily of nucleotidyltransferases.
13 ucleoside diphosphate sugars (NDP-sugars) by nucleotidyltransferases.
14 te a mitochondrial origin of the animal tRNA nucleotidyltransferases.
15 r to those found in cap-binding proteins and nucleotidyltransferases.
16 ic domain to DNA polymerase beta and related nucleotidyltransferases.
17 ans possesses separate CC- and A-adding tRNA nucleotidyltransferases.
18 ovo, by the CCA-adding enzyme [ATP(CTP):tRNA nucleotidyltransferase].
19 by 3'->5' exoribonuclease polyribonucleotide nucleotidyltransferase 1 (PNPT1) and has higher affinity
20 egulate the expression of polyribonucleotide nucleotidyltransferase 1 (PNPT1) resulting in the releas
21 suedo-trisaccharide, bound to aminoglycoside nucleotidyltransferase (2' ')-Ia has been determined usi
22 on of isepamicin bound to the aminoglycoside nucleotidyltransferase (2' ')-Ia, determined in this wor
26 y predecessors of cGAS called cGAS/DncV-like nucleotidyltransferases(2) (CD-NTases), which detect bac
28 enzymes, suggesting that these distinct tRNA nucleotidyltransferase activities can intraconvert over
29 one-pot" method to identify a range of sugar nucleotidyltransferase activities of purified proteins o
37 y the nsp12 NiRAN (nidovirus RdRp-associated nucleotidyltransferase), an enigmatic catalytic domain e
38 refore, non-mammalian cGAS may function as a nucleotidyltransferase and could produce cGAMP and other
40 n which a central catalytic core composed of nucleotidyltransferase and oligonucleotide-binding (OB)
41 mutant strains were constructed lacking tRNA nucleotidyltransferase and other enzymes potentially inv
42 re affected differently by reduced cytosolic nucleotidyltransferase and that cells resuming exponenti
44 s the stage for engineering single universal nucleotidyltransferases and also provides new catalysts
45 ors, HS90-type ATPase domains, archaeal tRNA nucleotidyltransferases and archaeal homologs of DnaG-ty
48 is enzyme Tyw3p, DNA/RNA ligases and related nucleotidyltransferases and the Enhancer of rudimentary
49 oly(A) polymerase, NTSFII as a C-adding tRNA nucleotidyltransferase, and NTSFIII as an A-adding tRNA
50 Rather, the two proteins function as tRNA nucleotidyltransferases, and our data suggest that, like
56 and a novel tRNA-like molecule) and a novel nucleotidyltransferase associating with diverse ligases.
59 he core subdomain is found not only in sugar nucleotidyltransferases but also in other nucleotidyltra
60 ctive site in Pol III that is not present in nucleotidyltransferases but which resembles an element a
61 synthetase adenylyltransferase or kanamycin nucleotidyltransferase, but provides the complete active
62 e N-terminal portion of Zcchc11, which lacks nucleotidyltransferase capabilities, is biologically act
63 s a distinctive modular structure in which a nucleotidyltransferase catalytic domain is flanked by an
70 des, then bind and activate a cGAS/DncV-like nucleotidyltransferase (CD-NTase) to generate a cyclic t
71 ow that operons with distinct cGAS/DncV-like nucleotidyltransferases (CD-NTases) and CD-NTase-associa
72 y et al. (2019) define a family of bacterial nucleotidyltransferases (CD-NTases) capable of synthesiz
73 nd discover a large family of cGAS/DncV-like nucleotidyltransferases (CD-NTases) that use both purine
74 causing variants in TRNT1, a gene encoding a nucleotidyltransferase critical for tRNA processing.
75 enylation are dependent on the same terminal-nucleotidyltransferases, CutA, and CutB, and we show thi
76 of a nick-binding site on the surface of the nucleotidyltransferase domain (Arg-200 and Arg-208); or
78 bifunctional enzyme comprising a cytoplasmic nucleotidyltransferase domain (IPCT) fused with a membra
79 NA-capping enzyme is composed of a catalytic nucleotidyltransferase domain and a noncatalytic oligonu
80 cteria that appear to consist of the minimal nucleotidyltransferase domain and may resemble the ances
81 it Rpb1 and more specifically between the CE nucleotidyltransferase domain and the phosphorylated CTD
82 erved in OAS derivatives that lack an active nucleotidyltransferase domain and, as indicated by the a
83 reby identified five new residues within the nucleotidyltransferase domain as being essential for Lig
84 endent DNA ligases consists of an N-terminal nucleotidyltransferase domain fused to a C-terminal OB d
85 nducted a structure-function analysis of the nucleotidyltransferase domain of Escherichia coli LigA,
86 n the NMN-binding domain (domain Ia) and the nucleotidyltransferase domain or comprise part of a nick
87 s, and independently, by fusions of a shared nucleotidyltransferase domain to structurally diverse fl
88 e nsp12 N-terminal nidovirus RdRp-associated nucleotidyltransferase domain, detailing a new pocket fo
89 OB domain moves quasi-statically toward the nucleotidyltransferase domain, pivoting about a short li
90 ignal transduction since, in addition to the nucleotidyltransferase domain, these proteins contain li
91 ted by a surface-accessible loop between the nucleotidyltransferase domain, which is common to all li
97 t the nsp12 NiRAN (nidovirus RdRp-associated nucleotidyltransferase) domain performs this reaction, a
98 the mouse OAS-like proteins with inactivated nucleotidyltransferase domains, which suggests that some
100 se (either ATP-grasp or RtcB superfamilies), nucleotidyltransferases, enzymes modifying RNA-termini f
101 Guanylyltransferases are members of the nucleotidyltransferase family and function in mRNA cappi
102 ast Trf4/5 are members of a newly identified nucleotidyltransferase family conserved from yeast to ma
103 s structural similarity to the template-free nucleotidyltransferase family of RNA modifying enzymes.
106 onal region in MiD51 that is not part of the nucleotidyltransferase fold blocked Drp1 recruitment and
108 expression, and synthetic utility of a sugar nucleotidyltransferase from any archaeal source and demo
109 We have analyzed the distribution of RNA nucleotidyltransferases from the family that includes po
110 rophosphokinase (prs) and polyribonucleotide nucleotidyltransferase genes (pnpA), a hypothetical prot
111 ture for the reaction catalyzed by kanamycin nucleotidyltransferase has been determined from kinetic
113 that deletion of MUT68, encoding a terminal nucleotidyltransferase in the alga Chlamydomonas reinhar
114 hat MenT3 is a robust cytidine specific tRNA nucleotidyltransferase in vitro, capable of modifying th
115 e nucleases resemble the RNase H-superfamily nucleotidyltransferases in folds, and share a two-metal-
117 S/dinucleotide-cyclase in Vibrio (DncV)-like nucleotidyltransferases) in these pathways link pathogen
118 ily of double-stranded RNA (dsRNA)-activated nucleotidyltransferases involved in pathogen sensing and
120 Another new family of bacterial and archaeal nucleotidyltransferases is predicted to function in sign
122 yses showed that ccna_01210, which encodes a nucleotidyltransferase, is required for CPG2 production.
124 suggests that the evolution of this type of nucleotidyltransferases may have included bursts of rapi
125 oughput assay system will greatly facilitate nucleotidyltransferase mechanistic and directed evolutio
126 structure is composed of a classical ligase nucleotidyltransferase module that is embellished by a u
127 enzyme during CCA addition and that a single nucleotidyltransferase motif adds all three nucleotides.
132 are located within counterparts of conserved nucleotidyltransferase motifs I (99KEDG102), Ia (118SK11
133 for nick ligation, which are located within nucleotidyltransferase motifs I, Ia, III, IIIa, IV and V
134 minal module Rnl1-(1-270) contains essential nucleotidyltransferase motifs I, IV, and V and suffices
137 of the SARS-CoV-2 nidovirus RdRp-associated nucleotidyltransferase (NiRAN) domain is essential for v
138 at the kinase-like nidovirus RdRp-associated nucleotidyltransferase (NiRAN) domain(5) of nsp12 transf
139 to have four distinct domains: an N-terminal nucleotidyltransferase (NT) domain; a central HD domain,
141 The cognate toxin, AbiEii, is a predicted nucleotidyltransferase (NTase) and member of the DNA pol
142 op nicked DNA as a C-shaped protein clamp: a nucleotidyltransferase (NTase) domain and an OB domain (
143 ic region comprising a DNA-binding domain, a nucleotidyltransferase (NTase) domain, and an oligonucle
145 ChVLig consists of three structural domains, nucleotidyltransferase (NTase), OB-fold, and latch, that
147 f candidate enzymes including members of the nucleotidyltransferase (Ntr) family and polynucleotide p
149 icity of the reaction catalyzed by kanamycin nucleotidyltransferase of kanamycin A with either ATP or
151 this interface PCI1 and the previously known nucleotidyltransferase/phosphorylated CTD interface PCI2
154 The addition of a general phosphatase to nucleotidyltransferase reaction aliquots enabled the con
155 ignificantly reduced ability to catalyze the nucleotidyltransferase reaction on the covalently immobi
157 s have a paucity of glycosyltransferases and nucleotidyltransferases recognizable by bioinformatics,
158 In addition to promoting an understanding of nucleotidyltransferase regulation by metabolites, this w
160 applicable high throughput sugar-1-phosphate nucleotidyltransferase screen and the first proof of con
161 tructures of human and insect cGLRs reveal a nucleotidyltransferase signalling core shared with cGAS
162 periments using a strain mutated in the Cca1 nucleotidyltransferase suggest that the uORF length-depe
164 terial species encode only one member of the nucleotidyltransferase superfamily (NTSF), and if that p
165 are likely to apply broadly to the covalent nucleotidyltransferase superfamily of RNA ligases, DNA l
166 o sequences encoding known members of an RNA nucleotidyltransferase superfamily that includes tRNA nu
167 , an ATP-dependent RNA-editing ligase of the nucleotidyltransferase superfamily that is required for
168 nserved domains found in the polymerase beta nucleotidyltransferase superfamily, which includes conve
177 e remodeled to bind a partner cGAS/DncV-like nucleotidyltransferase that is modified with an N-termin
178 A) polymerase activity and is instead a tRNA nucleotidyltransferase that repairs CCA ends of tRNAs.
179 ancer of decapping, or CutA, which encodes a nucleotidyltransferase that triggers mRNA decapping by t
180 d to study the class of enzymes called sugar nucleotidyltransferases that couple sugar-1-phosphates a
181 ng to the DNA polymerase beta superfamily of nucleotidyltransferases that share a conserved catalytic
182 TUTases), which are template-independent RNA nucleotidyltransferases that specifically recognize UTP
183 includes poly(A) polymerases (PAP) and tRNA nucleotidyltransferases (TNT) in 43 bacterial species.
186 ired by the CCA-adding enzyme (ATP(CTP):tRNA nucleotidyltransferase) using CTP and ATP as substrates
188 otic in the active site of an aminoglycoside nucleotidyltransferase was determined using the purified
190 ailed analysis of the polbeta superfamily of nucleotidyltransferases was performed using computer met
192 ses is homologous to the polbeta superfamily nucleotidyltransferases which emphasizes the general tre
193 ification of an archaeal gene encoding a new nucleotidyltransferase, which is proposed to be the nono
194 rial defense pathway integrating a cGAS-like nucleotidyltransferase with HORMA domain proteins for th
195 d these include aIF2alpha, a sugar-phosphate nucleotidyltransferase with sequence similarity to eIF2B
196 only describes a very narrow subset of these nucleotidyltransferases, with the vast majority fulfilli