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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 transferase, and NTSFIII as an A-adding tRNA nucleotidyltransferase.
7 ally by the CCA-adding enzyme, a specialized nucleotidyltransferase.
8 te a mitochondrial origin of the animal tRNA nucleotidyltransferases.
9 es and is a member of a large superfamily of nucleotidyltransferases.
10 ng that the basic mechanism is found in many nucleotidyltransferases.
11 ar nucleotidyltransferases but also in other nucleotidyltransferases.
12 cyclases and a family of DNA polymerases and nucleotidyltransferases.
13 of class I enzymes within the superfamily of nucleotidyltransferases.
14 r to those found in cap-binding proteins and nucleotidyltransferases.
15 ic domain to DNA polymerase beta and related nucleotidyltransferases.
16 ans possesses separate CC- and A-adding tRNA nucleotidyltransferases.
17 ovo, by the CCA-adding enzyme [ATP(CTP):tRNA nucleotidyltransferase].
18 suedo-trisaccharide, bound to aminoglycoside nucleotidyltransferase (2' ')-Ia has been determined usi
19 on of isepamicin bound to the aminoglycoside nucleotidyltransferase (2' ')-Ia, determined in this wor
24 enzymes, suggesting that these distinct tRNA nucleotidyltransferase activities can intraconvert over
25 one-pot" method to identify a range of sugar nucleotidyltransferase activities of purified proteins o
32 refore, non-mammalian cGAS may function as a nucleotidyltransferase and could produce cGAMP and other
34 n which a central catalytic core composed of nucleotidyltransferase and oligonucleotide-binding (OB)
35 mutant strains were constructed lacking tRNA nucleotidyltransferase and other enzymes potentially inv
36 re affected differently by reduced cytosolic nucleotidyltransferase and that cells resuming exponenti
38 s the stage for engineering single universal nucleotidyltransferases and also provides new catalysts
39 ors, HS90-type ATPase domains, archaeal tRNA nucleotidyltransferases and archaeal homologs of DnaG-ty
42 is enzyme Tyw3p, DNA/RNA ligases and related nucleotidyltransferases and the Enhancer of rudimentary
43 oly(A) polymerase, NTSFII as a C-adding tRNA nucleotidyltransferase, and NTSFIII as an A-adding tRNA
44 Rather, the two proteins function as tRNA nucleotidyltransferases, and our data suggest that, like
50 and a novel tRNA-like molecule) and a novel nucleotidyltransferase associating with diverse ligases.
53 he core subdomain is found not only in sugar nucleotidyltransferases but also in other nucleotidyltra
54 ctive site in Pol III that is not present in nucleotidyltransferases but which resembles an element a
55 synthetase adenylyltransferase or kanamycin nucleotidyltransferase, but provides the complete active
56 e N-terminal portion of Zcchc11, which lacks nucleotidyltransferase capabilities, is biologically act
57 s a distinctive modular structure in which a nucleotidyltransferase catalytic domain is flanked by an
62 causing variants in TRNT1, a gene encoding a nucleotidyltransferase critical for tRNA processing.
63 of a nick-binding site on the surface of the nucleotidyltransferase domain (Arg-200 and Arg-208); or
65 bifunctional enzyme comprising a cytoplasmic nucleotidyltransferase domain (IPCT) fused with a membra
66 NA-capping enzyme is composed of a catalytic nucleotidyltransferase domain and a noncatalytic oligonu
67 cteria that appear to consist of the minimal nucleotidyltransferase domain and may resemble the ances
68 it Rpb1 and more specifically between the CE nucleotidyltransferase domain and the phosphorylated CTD
69 erved in OAS derivatives that lack an active nucleotidyltransferase domain and, as indicated by the a
70 reby identified five new residues within the nucleotidyltransferase domain as being essential for Lig
71 nducted a structure-function analysis of the nucleotidyltransferase domain of Escherichia coli LigA,
72 n the NMN-binding domain (domain Ia) and the nucleotidyltransferase domain or comprise part of a nick
73 s, and independently, by fusions of a shared nucleotidyltransferase domain to structurally diverse fl
74 OB domain moves quasi-statically toward the nucleotidyltransferase domain, pivoting about a short li
75 ignal transduction since, in addition to the nucleotidyltransferase domain, these proteins contain li
76 ted by a surface-accessible loop between the nucleotidyltransferase domain, which is common to all li
81 the mouse OAS-like proteins with inactivated nucleotidyltransferase domains, which suggests that some
83 se (either ATP-grasp or RtcB superfamilies), nucleotidyltransferases, enzymes modifying RNA-termini f
85 ast Trf4/5 are members of a newly identified nucleotidyltransferase family conserved from yeast to ma
86 s structural similarity to the template-free nucleotidyltransferase family of RNA modifying enzymes.
89 onal region in MiD51 that is not part of the nucleotidyltransferase fold blocked Drp1 recruitment and
91 expression, and synthetic utility of a sugar nucleotidyltransferase from any archaeal source and demo
92 We have analyzed the distribution of RNA nucleotidyltransferases from the family that includes po
93 rophosphokinase (prs) and polyribonucleotide nucleotidyltransferase genes (pnpA), a hypothetical prot
94 ture for the reaction catalyzed by kanamycin nucleotidyltransferase has been determined from kinetic
96 that deletion of MUT68, encoding a terminal nucleotidyltransferase in the alga Chlamydomonas reinhar
97 e nucleases resemble the RNase H-superfamily nucleotidyltransferases in folds, and share a two-metal-
99 Another new family of bacterial and archaeal nucleotidyltransferases is predicted to function in sign
102 suggests that the evolution of this type of nucleotidyltransferases may have included bursts of rapi
103 oughput assay system will greatly facilitate nucleotidyltransferase mechanistic and directed evolutio
104 structure is composed of a classical ligase nucleotidyltransferase module that is embellished by a u
105 enzyme during CCA addition and that a single nucleotidyltransferase motif adds all three nucleotides.
110 are located within counterparts of conserved nucleotidyltransferase motifs I (99KEDG102), Ia (118SK11
111 for nick ligation, which are located within nucleotidyltransferase motifs I, Ia, III, IIIa, IV and V
112 minal module Rnl1-(1-270) contains essential nucleotidyltransferase motifs I, IV, and V and suffices
114 to have four distinct domains: an N-terminal nucleotidyltransferase (NT) domain; a central HD domain,
116 The cognate toxin, AbiEii, is a predicted nucleotidyltransferase (NTase) and member of the DNA pol
117 op nicked DNA as a C-shaped protein clamp: a nucleotidyltransferase (NTase) domain and an OB domain (
118 ic region comprising a DNA-binding domain, a nucleotidyltransferase (NTase) domain, and an oligonucle
119 ChVLig consists of three structural domains, nucleotidyltransferase (NTase), OB-fold, and latch, that
120 f candidate enzymes including members of the nucleotidyltransferase (Ntr) family and polynucleotide p
122 icity of the reaction catalyzed by kanamycin nucleotidyltransferase of kanamycin A with either ATP or
124 this interface PCI1 and the previously known nucleotidyltransferase/phosphorylated CTD interface PCI2
126 The addition of a general phosphatase to nucleotidyltransferase reaction aliquots enabled the con
127 ignificantly reduced ability to catalyze the nucleotidyltransferase reaction on the covalently immobi
129 s have a paucity of glycosyltransferases and nucleotidyltransferases recognizable by bioinformatics,
130 applicable high throughput sugar-1-phosphate nucleotidyltransferase screen and the first proof of con
131 periments using a strain mutated in the Cca1 nucleotidyltransferase suggest that the uORF length-depe
133 terial species encode only one member of the nucleotidyltransferase superfamily (NTSF), and if that p
134 are likely to apply broadly to the covalent nucleotidyltransferase superfamily of RNA ligases, DNA l
135 o sequences encoding known members of an RNA nucleotidyltransferase superfamily that includes tRNA nu
136 , an ATP-dependent RNA-editing ligase of the nucleotidyltransferase superfamily that is required for
137 nserved domains found in the polymerase beta nucleotidyltransferase superfamily, which includes conve
145 A) polymerase activity and is instead a tRNA nucleotidyltransferase that repairs CCA ends of tRNAs.
146 ancer of decapping, or CutA, which encodes a nucleotidyltransferase that triggers mRNA decapping by t
147 d to study the class of enzymes called sugar nucleotidyltransferases that couple sugar-1-phosphates a
148 ng to the DNA polymerase beta superfamily of nucleotidyltransferases that share a conserved catalytic
149 TUTases), which are template-independent RNA nucleotidyltransferases that specifically recognize UTP
150 includes poly(A) polymerases (PAP) and tRNA nucleotidyltransferases (TNT) in 43 bacterial species.
151 ired by the CCA-adding enzyme (ATP(CTP):tRNA nucleotidyltransferase) using CTP and ATP as substrates
152 otic in the active site of an aminoglycoside nucleotidyltransferase was determined using the purified
154 ailed analysis of the polbeta superfamily of nucleotidyltransferases was performed using computer met
156 ses is homologous to the polbeta superfamily nucleotidyltransferases which emphasizes the general tre
157 ification of an archaeal gene encoding a new nucleotidyltransferase, which is proposed to be the nono
158 d these include aIF2alpha, a sugar-phosphate nucleotidyltransferase with sequence similarity to eIF2B
159 only describes a very narrow subset of these nucleotidyltransferases, with the vast majority fulfilli
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