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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  the tubulin and specifically depends on the carboxy-terminal tails.
5 hrough an interaction at their intracellular carboxy-terminal tails.
6  the phosphorylation of the p70 noncatalytic carboxy-terminal tail (amino acids 422-525) and of amino
7 s are inserted into cellular membranes via a carboxy-terminal tail-anchor segment, but the mechanism
8 ying its FAD-binding pocket with a conserved carboxy-terminal tail and burying its PER-binding interf
9 p70 S6 kinase was also controlled by the p70 carboxy-terminal tail and by phosphorylation of p70 Ser3
10 associates constitutively with the channel's carboxy-terminal tail, and Ca2+ binding to the C-termina
11 flanked by two long alpha-helices and a long carboxy-terminal tail, and is stabilized by two bound zi
12 s: the positively charged amino-terminal and carboxy-terminal tails are separated by a globular domai
13 inding repeat, such as exons 2 and 3 and the carboxy-terminal tail, can greatly influence its polymer
14   DNA ligase IV is characterized by a unique carboxy-terminal tail comprising two BRCT (BRCA1 carboxy
15 ptors, signal through docking sites in their carboxy-terminal tails created by autophosphorylated tyr
16 to the third intracellular loop (i3) and the carboxy terminal tail (ct) of the 5-HT2AR.
17                             We show that the carboxy-terminal tail (CTT) of PC1 is released by gamma-
18  residues for DNA binding in cGAS as well as carboxy terminal tail domain for transducing signals in
19 lf-driven through interactions between K14's carboxy-terminal tail domain and two regions in the cent
20  to that of other myosins, whereas the large carboxy-terminal tail domain differs greatly from brush
21 main autoinhibited conformation in which the carboxy-terminal tail domain is held pincer-like by the
22 dimer formation through a coiled-coil, and a carboxy-terminal tail domain that binds light chains and
23  large number of multiple KSP repeats in the carboxy-terminal tail domain, which are phosphorylation
24 ro) (KSP) multiple amino acid repeats of the carboxy-terminal tail domain.
25   Here we investigate the negatively charged carboxy-terminal tail domains (CTTs) of alpha- and beta-
26 in vivo, whereas mutations in the amino- and carboxy-terminal tails have no detectable effect.
27  (CP) in the mature proteasome, with the Rpt carboxy-terminal tails inserting into pockets of the alp
28  Tpl-2 protein and a GST fusion of the Tpl-2 carboxy-terminal tail interact when coexpressed in Sf9 c
29                       We have shown that the carboxy-terminal tail is the key targeting region and ha
30                                      Using a carboxy-terminal-tail mutant of K. lactis RAP1, we also
31 e junction components contain unusually long carboxy-terminal tails not found in those family members
32 lving serine residues 324 and 325 within the carboxy-terminal tail of CXCR4.
33                 We find that a region in the carboxy-terminal tail of DNA ligase IV located between r
34 the juxtamembrane region, kinase domain, and carboxy-terminal tail of EphB2 and EphB5, and found to b
35  unique amino-terminal domain that binds the carboxy-terminal tail of Gli1.
36 nuclein variants and residues 598-620 of the carboxy-terminal tail of hDAT, in both trypsinized and n
37 P4, has previously been shown to bind to the carboxy-terminal tail of MTA1.
38                                  The lumenal carboxy-terminal tail of Pex15p protrudes into the lumen
39 orylates a conserved tyrosine residue in the carboxy-terminal tail of Src [7] [8].
40                                          The carboxy-terminal tail of TFAM is essential for activatio
41  demonstrate that the connecting segment and carboxy-terminal tail of the beta4 cytoplasmic domain in
42                               The methylated carboxy-terminal tail of the C subunit interacts with a
43 ic acid of the second drug molecule near the carboxy-terminal tail of the enzyme.
44 dentify serine residue 1166 (Ser1166) in the carboxy-terminal tail of the NMDAR subunit GluN2B to be
45 in vitro via pTyr sites 1068 and 1086 in the carboxy-terminal tail of the receptor and that overexpre
46  are also able to directly interact with the carboxy-terminal tail of the transverse tubule dihydropy
47 his activation requires histidine 711 in the carboxy-terminal tail of TRPV5.
48 ules by recognizing specific features in the carboxy-terminal tail of tubulin.
49                                          The carboxy-terminal tail of ubiquitin is locked into an act
50        Adrm1 (human Rpn13, hRpn13) binds the carboxy-terminal tail of Uch37, a region that is distinc
51 e last ten amino acid residues in the basic, carboxy-terminal tail of yeast rpS14 for binding to RNA,
52                Recent work suggests that the carboxy-terminal tails of these conserved proteins are u
53        The posttranslational modification of carboxy-terminal tails of tubulin plays an important rol
54 with the extracellular face, rather than the carboxy-terminal tail, of the receptors.
55  regulated by interactions with the helicase carboxy-terminal tail peptides.
56 nt (NF) proteins are phosphorylated in their carboxy-terminal tail portion by the enzyme cyclin-depen
57                                         PA26 carboxy-terminal tails provide binding affinity by inser
58 oth alpha- and beta-tubulin proteins possess carboxy-terminal tail regions (CTTs) that are negatively
59 substitutions within the zinc finger and the carboxy-terminal tail result in a loss of nitrogen metab
60 mRNA and that differs from Hac1pu by a short carboxy-terminal tail sequence.
61 s by phosphorylating a serine residue in the carboxy-terminal tail SQE motif of histone H2AX.
62                      CRYs contain a variable carboxy-terminal tail that appends the conserved PL homo
63 nnected by a short basic linker to an acidic carboxy-terminal tail that differs in length between HMG
64 is core is stabilized in part by an extended carboxy-terminal tail that locks the molecule into an in
65 h are variously modified at their amino- and carboxy-terminal tails to influence the dynamics of chro
66 investigate the inhibition effect of tubulin carboxy-terminal tails using peptide sequences of alpha-

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