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1 4, an uncharacterized mitochondrial putative pseudouridine synthase.
2 morphic alleles of nop60B, a gene encoding a pseudouridine synthase.
3 id residue is catalytically essential in one pseudouridine synthase.
4 antly alter the catalytic activity of either pseudouridine synthase.
5 uridine (or pseudouridylation) catalyzed by pseudouridine synthases.
6 ends on both site-specific and snoRNA-guided pseudouridine synthases.
7 ficant relative to turnover by the wild-type pseudouridine synthases.
8 to these previously identified ribosomal RNA pseudouridine synthases.
11 tified a homozygous missense mutation in the pseudouridine synthase 1 gene (PUS1) in all patients wit
13 redicted protein has 34% identity with yeast pseudouridine synthase 3 (Pus3), an enzyme known to form
15 in the ribosomal protein S4, two families of pseudouridine synthases, a novel family of predicted RNA
16 oned, overexpressed, and shown to code for a pseudouridine synthase able to react with in vitro trans
17 de that the conserved Asp60 is essential for pseudouridine synthase activity and propose mechanisms w
18 r novel domain, designated PUA domain, after PseudoUridine synthase and Archaeosine transglycosylase,
19 rate bound to the ribonucleoprotein particle pseudouridine synthase and enzyme activity assay confirm
20 ery similar to the catalytic domain of other pseudouridine synthases and a second large domain (149 a
21 tural properties that are unique among known pseudouridine synthases and are consistent with its dist
22 he downstream genes ppnK (NAD kinase), rluE (pseudouridine synthase), and pta (phosphotransacetylase)
24 roteins, including ribosomal protein S4, RNA pseudouridine synthase, and tyrosyl-tRNA synthetase.
25 ase, was detected in archaeal and eukaryotic pseudouridine synthases, archaeal archaeosine synthases,
28 roline residues in Motif I of RluA and TruB, pseudouridine synthases belonging to different families.
34 stand alone pseudouridine synthases, the RNP pseudouridine synthase comprises multiple protein subuni
35 e, TERC, and other components, including the pseudouridine synthase, dyskerin, the product of the DKC
36 ight of the global dissimilarity between the pseudouridine synthase families, we changed the aspartic
37 ture of the RNA-modifying enzyme, psi55 tRNA pseudouridine synthase from Mycobacterium tuberculosis,
38 ue is critical for the catalytic activity of pseudouridine synthases from two additional families of
39 of macrophages with a F. tularensis LVS rluD pseudouridine synthase (FTL_0699) mutant resulted in dim
40 our findings also support the assignment of pseudouridine synthase function to certain physiological
44 tRNA caused a time-dependent inactivation of pseudouridine synthase I and formed a covalent complex w
47 de a resource for identifying the targets of pseudouridine synthases implicated in human disease.
49 s little sequence homology with the other 10 pseudouridine synthases in E. coli which themselves have
51 Analysis of total tRNA isolated from E. coli pseudouridine synthase knock-out mutants identified RluF
52 guide RNA and four essential proteins: Cbf5 (pseudouridine synthase), L7Ae, Gar1 and Nop10 in archaea
53 e alignments using the first four identified pseudouridine synthases led Koonin and, independently, S
54 pseudouridine synthases (PUS) uncovers which pseudouridine synthase modifies each site and their targ
56 ry to probe the role of cysteine residues in pseudouridine synthases of the families that do not incl
57 ence and structural comparisons suggest that pseudouridine synthases of the RluA, RsuA, and TruA fami
58 The predicted SwoCp is homologous to rRNA pseudouridine synthases of yeast (Cbf5p) and humans (Dkc
59 f the TruA, TruB, RsuA, and RluA families of pseudouridine synthases (PsiS) identifies a strictly con
60 tructural comparisons with other families of pseudouridine synthases (PsiS) indicate that Psi55S may
65 The Escherichia coli rluD gene encodes a pseudouridine synthase responsible for the pseudouridine
66 e Escherichia coli gene rluA, coding for the pseudouridine synthase RluA that forms 23 S rRNA pseudou
69 idine, bound to a ribonucleoprotein particle pseudouridine synthase, strongly prefer the syn glycosid
71 Mutations in DKC1, encoding for dyskerin, a pseudouridine synthase that modifies rRNA and regulates
72 n that there are four distinct "families" of pseudouridine synthases that share no statistically sign
73 an active site cleft, conserved in all other pseudouridine synthases, that contains invariant Asp and
75 ar ribonucleoprotein complexes and acts as a pseudouridine synthase to modify newly synthesized ribos
79 we prove the tRNA chaperone activity of the pseudouridine synthase TruB, reveal its molecular mechan
82 Asp60, conserved in all known and putative pseudouridine synthases, was mutated to amino acids with
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