ライフサイエンスコーパス: carboxy-terminal tail

1 t provided fusion of TetA to a polyhistidine-carboxy terminal tail.

2 vates Pol I transcription through its acidic carboxy-terminal tail.

3 linked by a short basic region to an acidic carboxy-terminal tail.

4 dependent on the presence of the desmoplakin carboxy-terminal tail.

5 hrough an interaction at their intracellular carboxy-terminal tails.

6 the tubulin and specifically depends on the carboxy-terminal tails.

7 the phosphorylation of the p70 noncatalytic carboxy-terminal tail (amino acids 422-525) and of amino

8 s are inserted into cellular membranes via a carboxy-terminal tail-anchor segment, but the mechanism

9 ying its FAD-binding pocket with a conserved carboxy-terminal tail and burying its PER-binding interf

10 p70 S6 kinase was also controlled by the p70 carboxy-terminal tail and by phosphorylation of p70 Ser3

11 s with the increased ubiquitination of EphB4 carboxy-terminal tail and with its rapid degradation.

12 associates constitutively with the channel's carboxy-terminal tail, and Ca2+ binding to the C-termina

13 flanked by two long alpha-helices and a long carboxy-terminal tail, and is stabilized by two bound zi

14 s: the positively charged amino-terminal and carboxy-terminal tails are separated by a globular domai

15 glutamates to internal glutamates in tubulin carboxy-terminal tails (branch initiation, through an is

16 inding repeat, such as exons 2 and 3 and the carboxy-terminal tail, can greatly influence its polymer

17 DNA ligase IV is characterized by a unique carboxy-terminal tail comprising two BRCT (BRCA1 carboxy

18 ptors, signal through docking sites in their carboxy-terminal tails created by autophosphorylated tyr

19 to the third intracellular loop (i3) and the carboxy terminal tail (ct) of the 5-HT2AR.

20 tors, the third intracellular loop (IL3) and carboxy-terminal tail (CT) are sites for G protein-coupl

21 We show that the carboxy-terminal tail (CTT) of PC1 is released by gamma-

22 Carboxy-terminal tails (CTTs) of tubulin proteins are si

23 residues for DNA binding in cGAS as well as carboxy terminal tail domain for transducing signals in

24 lf-driven through interactions between K14's carboxy-terminal tail domain and two regions in the cent

25 to that of other myosins, whereas the large carboxy-terminal tail domain differs greatly from brush

26 main autoinhibited conformation in which the carboxy-terminal tail domain is held pincer-like by the

27 dimer formation through a coiled-coil, and a carboxy-terminal tail domain that binds light chains and

28 large number of multiple KSP repeats in the carboxy-terminal tail domain, which are phosphorylation

29 ro) (KSP) multiple amino acid repeats of the carboxy-terminal tail domain.

30 xy-terminal RNA-binding domain (CTD) and the carboxy-terminal tail (domain N3) both have roles in PS

31 Here we investigate the negatively charged carboxy-terminal tail domains (CTTs) of alpha- and beta-

32 in vivo, whereas mutations in the amino- and carboxy-terminal tails have no detectable effect.

33 (CP) in the mature proteasome, with the Rpt carboxy-terminal tails inserting into pockets of the alp

34 Tpl-2 protein and a GST fusion of the Tpl-2 carboxy-terminal tail interact when coexpressed in Sf9 c

35 We have shown that the carboxy-terminal tail is the key targeting region and ha

36 Using a carboxy-terminal-tail mutant of K. lactis RAP1, we also

37 e junction components contain unusually long carboxy-terminal tails not found in those family members

38 opts an autoinhibited conformation where its carboxy-terminal tail occupies the cargo binding groove.

39 lving serine residues 324 and 325 within the carboxy-terminal tail of CXCR4.

40 The carboxy-terminal tail of CXCR5 contains several serine/t

41 We find that a region in the carboxy-terminal tail of DNA ligase IV located between r

42 the juxtamembrane region, kinase domain, and carboxy-terminal tail of EphB2 and EphB5, and found to b

43 unique amino-terminal domain that binds the carboxy-terminal tail of Gli1.

44 nuclein variants and residues 598-620 of the carboxy-terminal tail of hDAT, in both trypsinized and n

45 d fractionation reveal that the unstructured carboxy-terminal tail of MBNL1 allows for anchoring at m

46 P4, has previously been shown to bind to the carboxy-terminal tail of MTA1.

47 The lumenal carboxy-terminal tail of Pex15p protrudes into the lumen

48 orylates a conserved tyrosine residue in the carboxy-terminal tail of Src [7] [8].

49 The carboxy-terminal tail of TFAM is essential for activatio

50 demonstrate that the connecting segment and carboxy-terminal tail of the beta4 cytoplasmic domain in

51 The methylated carboxy-terminal tail of the C subunit interacts with a

52 the mechanism through which the unstructured carboxy-terminal tail of the cargo adaptor sorting nexin

53 ic acid of the second drug molecule near the carboxy-terminal tail of the enzyme.

54 dentify serine residue 1166 (Ser1166) in the carboxy-terminal tail of the NMDAR subunit GluN2B to be

55 in vitro via pTyr sites 1068 and 1086 in the carboxy-terminal tail of the receptor and that overexpre

56 The carboxy-terminal tail of the severe acute respiratory sy

57 are also able to directly interact with the carboxy-terminal tail of the transverse tubule dihydropy

58 his activation requires histidine 711 in the carboxy-terminal tail of TRPV5.

59 ules by recognizing specific features in the carboxy-terminal tail of tubulin.

60 The carboxy-terminal tail of ubiquitin is locked into an act

61 Adrm1 (human Rpn13, hRpn13) binds the carboxy-terminal tail of Uch37, a region that is distinc

62 e last ten amino acid residues in the basic, carboxy-terminal tail of yeast rpS14 for binding to RNA,

63 rimed for ubiquitin transfer to the flexible carboxy-terminal tails of H2A and variant H2AX.

64 Recent work suggests that the carboxy-terminal tails of these conserved proteins are u

65 The posttranslational modification of carboxy-terminal tails of tubulin plays an important rol

66 with the extracellular face, rather than the carboxy-terminal tail, of the receptors.

67 regulated by interactions with the helicase carboxy-terminal tail peptides.

68 nt (NF) proteins are phosphorylated in their carboxy-terminal tail portion by the enzyme cyclin-depen

69 PA26 carboxy-terminal tails provide binding affinity by inser

70 oth alpha- and beta-tubulin proteins possess carboxy-terminal tail regions (CTTs) that are negatively

71 substitutions within the zinc finger and the carboxy-terminal tail result in a loss of nitrogen metab

72 mRNA and that differs from Hac1pu by a short carboxy-terminal tail sequence.

73 s by phosphorylating a serine residue in the carboxy-terminal tail SQE motif of histone H2AX.

74 CRYs contain a variable carboxy-terminal tail that appends the conserved PL homo

75 nnected by a short basic linker to an acidic carboxy-terminal tail that differs in length between HMG

76 is core is stabilized in part by an extended carboxy-terminal tail that locks the molecule into an in

77 h are variously modified at their amino- and carboxy-terminal tails to influence the dynamics of chro

78 investigate the inhibition effect of tubulin carboxy-terminal tails using peptide sequences of alpha-

79 eting post-translational modification of its carboxy-terminal tail via phosphorylation of its tyrosin

80 interacts with SMAD2 and TGFBR2 through its carboxy-terminal tail, which enhances TGFbeta signalling

81 tameric ring around a region of the receptor carboxy-terminal tail, while a second KCTD domain, H1, e