ライフサイエンスコーパス: mRNA capping enzyme

1 did not affect the function of TFIIS or the mRNA capping enzyme.

2 and Cet1p, the two subunits of the yeast pre-mRNA capping enzyme.

3 ligase fused to the C-terminal domain 2 of a mRNA capping enzyme.

4 iphosphatase domain of the metazoan cellular mRNA capping enzyme.

5 ture-sensitive mutations of Ceg1p, the yeast mRNA capping enzyme.

6 ATP-dependent DNA ligases and GTP-dependent mRNA capping enzymes.

7 triphosphatase domains of metazoan and plant mRNA capping enzymes.

8 cture in Rnl2-like ligases, DNA ligases, and mRNA capping enzymes.

9 completely different from those of mammalian mRNA capping enzymes.

10 vaccinia virus and Saccharomyces cerevisiae mRNA capping enzymes.

11 5' end of nascent mRNA is carried out by the mRNA-capping enzyme, a two-domain protein that is a memb

12 large protein (L), along with unconventional mRNA capping enzymes: a GDP:polyribonucleotidyltransfera

13 e and with previously reported structures of mRNA capping enzymes, adenylate cyclases, and polyphosph

14 Spt5 also coimmunopurified with the mRNA capping enzyme and cap methyltransferase, and spt4

15 f conformational rearrangements spanning all mRNA-capping enzymes and all ATP-dependent DNA ligases.

16 Virus-encoded mRNA capping enzymes are attractive targets for antivira

17 Eukaryotic mRNA capping enzymes are bifunctional, carrying both RNA

18 mRNA-capping enzyme binds only to phosphorylated CTD, wh

19 gating RNA polymerase II, and recruitment of mRNA capping enzyme, cap-binding complex, and 3' end for

20 The 317 residue PBCV-1 mRNA capping enzyme catalyzes the second enzymatic react

21 Recruitment of the mRNA capping enzyme (CE/RNGTT) to the site of transcript

22 In vitro, the yeast mRNA capping enzymes Ceg1 and Abd1 bind specifically to

23 All known eukaryotic and some viral mRNA capping enzymes (CEs) transfer a GMP moiety of GTP

24 We have recently demonstrated that an mRNA capping enzyme, Cet1, impairs promoter-proximal acc

25 in vivo and in vitro to form a bifunctional mRNA capping enzyme complex.

26 in vivo and in vitro to form a bifunctional mRNA capping enzyme complex.

27 The Saccharomyces cerevisiae mRNA capping enzyme consists of two subunits: an RNA 5'-

28 The Saccharomyces cerevisiae mRNA capping enzyme consists of two subunits: the RNA 5'

29 closest homologs, which include the metazoan mRNA capping enzymes, constitute a subgroup of the PTP f

30 The mRNA guanylyltransferase, or mRNA capping enzyme, cotranscriptionally caps the 5'-end

31 NTase domain independently of the eukaryotic mRNA capping enzyme during evolution and PRNTase becomes

32 cruitment and exchange of factors, including mRNA capping enzymes, elongation factors, splicing facto

33 nts a functionally independent domain of the mRNA capping enzyme, fully competent in substrate bindin

34 bies virus (RABV), possess an unconventional mRNA capping enzyme (GDP polyribonucleotidyltransferase,

35 The unconventional mRNA capping enzyme (GDP polyribonucleotidyltransferase,

36 viruses that is distinct from the eukaryotic mRNA capping enzyme, guanylyltransferase.

37 nding mode different from that of eukaryotic mRNA capping enzyme, guanylyltransferase.

38 A new mRNA capping enzyme has been identified, PCIF1/CAPAM, wh

39 7 methyltransferase domain of vaccinia virus mRNA capping enzyme is a heterodimer composed of a catal

40 Vaccinia virus mRNA capping enzyme is a multifunctional protein with RN

41 to 545) of the D1 subunit of vaccinia virus mRNA capping enzyme is an autonomous bifunctional domain

42 The mRNA capping enzyme is characterized, in part, by a cons

43 thyltransferase domain of the vaccinia virus mRNA capping enzyme is composed of the C-terminal portio

44 phatase domain of the Caenorhabditis elegans mRNA capping enzyme is related to the PTP enzyme family

45 The mRNA-capping enzyme is composed of a catalytic nucleotid

46 the CTD the ability to recruit the mammalian mRNA capping enzyme (Mce1) and stimulate its guanylyltra

47 a biochemical and genetic analysis of mouse mRNA capping enzyme (Mce1), a bifunctional 597-amino aci

48 yltransferase (PRNTase) is an unconventional mRNA capping enzyme of NNS RNA viruses that is distinct

49 omain of the large subunit of vaccinia virus mRNA capping enzyme possessing ATPase, RNA 5'-triphospha

50 tural differences between poxvirus and human mRNA capping enzymes recommend cap formation as a target

51 iption initiation factor subunits A8 and D6; mRNA capping enzyme subunits D1 and D12; RNA cap 2'-O-me

52 103R protein of Chlorella virus PBCV-1 is an mRNA capping enzyme that catalyzes the transfer of GMP f

53 An interaction network connecting mRNA capping enzymes, the RNA polymerase II (Pol II) car

54 While our results are specific to the PBCV-1 mRNA capping enzyme, they provide a useful context withi

55 owth is circumvented by covalently tethering mRNA capping enzymes to the CTD, thus proving that cappi

56 Using purified human mRNA-capping enzymes, we show biochemically that efficie

57 transferase activities of the vaccinia virus mRNA capping enzyme were previously localized to an NH2-

58 mpared to complexes of T7 ligase with ATP or mRNA capping enzyme with GTP.

59 d baculovirus LEF4 protein is a bifunctional mRNA capping enzyme with triphosphatase and guanylyltran

60 d baculovirus Lef4 protein is a bifunctional mRNA capping enzyme with triphosphatase and guanylyltran