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1 a turn around residues 25-27, resulting in a helix-loop-helix motif.
2 transcription factor that contains the basic helix-loop-helix motif.
3 lls but only in the presence of the adjacent helix-loop-helix motif.
4 f Foxa2 knockdown also required the adjacent helix-loop-helix motif.
5 t both Fis1 and the second helix of the Mdv1 helix-loop-helix motif.
6 que tetrameric organization composed of four helix-loop-helix motifs.
7 Both proteins possess basic helix-loop-helix motifs.
8 rlier work, de novo designed peptides with a helix-loop-helix motif and 63 residues have been synthes
9 lved in two structural motifs: an N-terminal helix-loop-helix motif and a C-terminal three-helix bund
10 flexible linkage between the CcpA helix-turn-helix-loop-helix motif and hinge helices, which allows i
11 five or six direct repeats, each containing helix--loop--helix motifs, and, thus, belongs to the TFI
12 studies, Mdv1 binds Fis1 through a U-shaped helix-loop-helix motif, and dimerization of the Mdv1-Fis
13 ) of the coat protein through its C-terminal helix-loop-helix motif, as well as unexpected interactio
16 oducts of this gene contain the basic domain helix-loop-helix motif characteristic of a family of tra
18 01 located immediately outside the predicted helix-loop-helix motif completely abolished toxin activi
20 expectedly, the predicted leucine zipper and helix-loop-helix motifs do not form these structures but
22 However, these data do not distinguish the helix-loop-helix motif from a continuous helix, because
23 -repeats, R1-R6, each containing a potential helix-loop-helix motif implicated in protein-protein int
24 potent neutralizing antibody that binds to a helix-loop-helix motif in the RSV fusion glycoprotein.
27 and Ser(338) may also function with a nearby helix-loop-helix motif located at residues 339-372 to en
28 d through their leucine zipper motifs, their helix-loop-helix motifs may be involved in interactions
32 predicted zinc finger domain, and a putative helix-loop-helix motif, respectively, while the fourth c
33 yme, a small catalytic RNA consisting of two helix-loop-helix motifs, serves as a paradigm for RNA fo
34 ture of gp6 reveals a dimeric protein with a helix-loop-helix motif similar to that of bacteriophage
35 domain of P22 scaffolding protein exhibits a helix-loop-helix motif stabilized by a hydrophobic core.
38 c core domain and C-terminal domain adopts a helix-loop-helix motif that is similar to the correspond
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