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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
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
25 Here we investigate the negatively charged carboxy-terminal tail domains (CTTs) of alpha- and beta-
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
31 e junction components contain unusually long carboxy-terminal tails not found in those family members
34 the juxtamembrane region, kinase domain, and carboxy-terminal tail of EphB2 and EphB5, and found to b
36 nuclein variants and residues 598-620 of the carboxy-terminal tail of hDAT, in both trypsinized and n
41 demonstrate that the connecting segment and carboxy-terminal tail of the beta4 cytoplasmic domain in
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
51 e last ten amino acid residues in the basic, carboxy-terminal tail of yeast rpS14 for binding to RNA,
56 nt (NF) proteins are phosphorylated in their carboxy-terminal tail portion by the enzyme cyclin-depen
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
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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