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1 es share a short region of homology at their amino termini.
2 the presence of polypeptides with differing amino termini.
3 is evolving more slowly than the carboxy and amino termini.
4 d glycosylation sites in their extracellular amino termini.
5 of the changes occurring in the carboxyl and amino termini.
6 ologous DNA-binding domains located at their amino termini.
7 referentially produces Abetan-42 with ragged amino termini.
8 tinct scissile bonds located within receptor amino termini.
9 Selected peptides were sequenced from their amino termini.
10 ably because of lipid modifications at their amino termini.
11 l, differing only in a short region of their amino termini.
12 highly disrupted by exchange of the histone amino termini.
13 and 20 amino acids, respectively, from their amino termini.
14 ing of trimeric subunits associated at their amino termini.
15 very similar to, the murine isoforms in the amino termini.
16 glucoamylase (GH15)-like domains near their amino termini.
17 ia a conserved coiled-coil domain near their amino termini.
18 e a characteristic sialidase domain at their amino termini.
19 the diversity clustered at the carboxyl and amino termini.
20 hotyrosine binding (PH-PTB) domains at their amino termini.
21 2B1a and SULT2B1b, that differ only at their amino termini.
22 nteract with cell surface CD44 through their amino termini.
23 o not code for a coiled-coil domain in their amino termini.
24 des for two peptides differing only at their amino termini.
25 between the novel putative human and murine amino termini.
26 ly by attaching the M and L domains to their amino termini.
27 -e1 or MeCP2-e2 protein isoforms with unique amino termini.
28 roteins containing signal sequences at their amino termini.
29 s (mPanK1alpha and mPanK1beta) with distinct amino termini.
30 lated Met blocking group at their respective amino-termini.
31 I, II, and III) that differ at their extreme amino-termini.
32 ta(2e)) that differed only in their proximal amino-termini.
33 proteins share significant homology at their amino termini and a strong spatial conservation of cyste
34 ich have homology within a MADS box at their amino termini and an adjacent motif known as the MEF2 do
35 ial interactions do not involve the receptor amino termini and are not because of the charged nature
36 ty of Pbx and Meis to interact through their amino termini and bind DNA without stringent half-site o
37 Peptides are labeled predominantly at their amino termini and exhibit elution profiles that are inde
38 tent transcriptional activation domains, the amino termini and homeodomains have repressive activitie
40 TEF isoforms differ from each other at their amino termini and result from alternative promoter usage
42 ence mutants that contain negatively charged amino termini and simplified core regions of varying hyd
43 gests that modifications of both the histone amino termini and the core domain of nucleosomes contrib
44 , NERF-1b, and NERF-2, which differ in their amino termini and their expression in different tissues.
46 AtFNR isoforms contain multiple alternative amino termini and undergo light-responsive addition of a
48 d the contributions of the histone H3 and H4 amino termini, and of the coactivator and histone acetyl
49 that cleave at preferred amino acids, while amino termini appear to be determined more by proximity
50 forms of the antigen having either lipidated amino termini, approximating the natural secretion and p
51 basic (type 1) or large hydrophobic (type 2) amino termini are assumed to be targeted through this pa
52 partially hydrolyzed and the liberated alpha-amino termini are derivatized with an equimolar mixture
54 tution experiments, we find that the histone amino termini are important for nucleosome assembly in v
56 t additional regions towards the carboxy and amino termini are required for a stable interaction betw
57 ored is the extent to which specific histone amino termini are required for the activating and repres
58 conclude that ASCT2 isoforms with truncated amino termini are synthesized in mammalian cells by a le
59 Post-translational modifications of histone amino termini are thought to convey epigenetic informati
61 constructed of ten alpha-helices with their amino termini arrayed in a right-handed super-helical co
62 nally distinct isoforms that differ in their amino termini but share common LIM domains and a homeodo
63 (EcR-A, EcR-B1, and EcR-B2) that have unique amino termini but that contain a common carboxy-terminal
65 Intermolecular FRET indicated that the NS5A amino termini, but not other regions, are in close proxi
69 terface, residues located at the carboxy and amino termini contribute close to 75% of the total Gibbs
72 s few as four matrix residues fused to their amino-termini formed spheres in vitro, but that removing
75 oded by exons 2 and 3, but possess different amino termini, generated by alternative splicing of RNA
76 osttranslational acetylation of core histone amino termini has long been associated with transcriptio
80 In vitro, this externalization of the VP1 amino termini is accompanied by the release of the viral
81 e gene regulatory potential of the H3 and H4 amino termini is substantially but not entirely containe
83 n kinase kinase (MAPKK) family near to their amino termini, leading to the inhibition of one or more
84 ic domain that hydrolyzes cAMP and cGMP; the amino-termini (N-termini) vary in length and amino acid
86 ptide coupling at corresponding carboxyl and amino termini of (S)-valine-based bis-thiazole and monot
87 alysis confirmed two proteins with divergent amino termini of 285 residues and identical carboxyl ter
89 es for MMP-7 cleavage are more common at the amino termini of alpha-defensin rather than beta-defensi
93 mitochondrial localization sequences in the amino termini of both the human and Drosophila proteins.
99 cture to interact with the bound ligand: the amino termini of helices 3 and 9, the two beta sheets, h
100 ications of cytosine residues in DNA and the amino termini of histone proteins have emerged as key me
101 s include both covalent modifications of the amino termini of histones as well as ATP-dependent non-c
103 t with mono- and dimethylated lysines in the amino termini of histones H4 and H1b to promote methylat
104 ome MHC molecules are capable of binding the amino termini of intact cell surface proteins through th
105 RF5 interaction occurred on the carboxyl and amino termini of IRF5; a single internal deletion from a
108 of the new enzyme is more homologous to the amino termini of other bacterial glycosyltransferases th
109 The amino terminus of RstR is similar to the amino termini of other phage-encoded repressors, and Rst
110 lyzes the hydrolysis of amino acids from the amino termini of peptides with a prolyl residue in the s
111 l claimed specificity of PAO for the primary amino termini of polyamines, all of which are consistent
112 isplay library, and sequences similar to the amino termini of proapoptotic Drosophila proteins in the
115 osphatase (ATPase) mediates extrusion of the amino termini of secreted proteins from the eubacterial
121 ix formation appears just at the carboxy and amino termini of the first and third helices, respective
123 AC1-like domain, that is also present at the amino termini of the inositol polyphosphate 5-phosphatas
126 evealed that the GST domains and, hence, the amino termini of the RyR3 subunits are located in the "c
128 or absence of an additional arginine at the amino termini of their mature peptides, indicative of al
130 -2), four short amphipathic helices near the amino termini of these proteins have been proposed to ac
131 plicing of their progenitor mRNAs joined the amino termini of these proteins to the NP1 open reading
133 CM7 form protein complexes in vitro, and the amino termini of two Rb-related proteins, p107 and p130,
135 criminate between, e.g., signal peptides and amino-termini of cytosolic proteins with the lowest numb
137 suggest conformational changes occur in the amino-termini of Galpha(i) proteins upon subunit dissoci
140 ngs demonstrate that key residues within the amino-termini of two nearly identical proteins influence
141 Posttranslational modifications of histone amino termini play an important role in modulating chrom
146 de hydrophobic portions in their carboxy and amino termini, serving as transmembrane domains for CD39
147 uggesting that Slack channels with alternate amino-termini such as Slack-A channels are present at th
148 4 genes encode hydrophobic portions in their amino termini, suggesting that they might encode secrete
149 Because Naa10 is reported to acetylate all amino termini that are devoid of methionine and Naa50 ac
150 ncodes multiple ASCT2 isoforms with distinct amino termini that are translationally initiated by a le
151 were found to be repressed by the H3 and H4 amino termini under non-inducing conditions, indicating
153 erate a complex in which the motion of their amino termini was restricted, whereas complexes of low a
155 d and Rem differ significantly only in their amino-termini, we constructed Rad-Rem chimeras to probe
156 , contain a proline-rich region within their amino termini which may interact with other proteins.
157 isoforms, MeCP2e1 and MeCP2e2, with distinct amino termini, which are generated by alternative splici
159 of PKGs involves sequences located near the amino termini, which contain a conserved, extended leuci
160 CpTSP9, contain predicted introns near their amino termini, which were verified by comparing PCR prod
162 ity-purified peptides were modified at their amino termini with the fluorescent reagent 6-aminoquinol
163 ha1A, alpha1B, alpha1D) were tagged at their amino-termini with Flag or hemagglutinin epitopes and tr
164 as IA and IB isoforms which bear alternative amino termini, with the IB isoform containing a potentia
165 over 80% homologous outside of their unique amino termini, yet several studies suggest that differen
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