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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 rinsically disordered regions separated by a helix-loop-helix motif and that this structure is conser
12  five or six direct repeats, each containing helix--loop--helix motifs, and, thus, belongs to the TFI
13  studies, Mdv1 binds Fis1 through a U-shaped helix-loop-helix motif, and dimerization of the Mdv1-Fis
14 ) of the coat protein through its C-terminal helix-loop-helix motif, as well as unexpected interactio
15  In both cases, the dimer is stabilized by a helix-loop-helix motif at the C terminus and interaction
16       The two proteins differ in their basic helix-loop-helix motifs (bHLH), responsible for DNA bind
17  of transcription factors containing a basic helix-loop-helix motif can bind.
18 oducts of this gene contain the basic domain helix-loop-helix motif characteristic of a family of tra
19                  The structure comprises two helix-loop-helix motifs characteristic of EF-hand domain
20 01 located immediately outside the predicted helix-loop-helix motif completely abolished toxin activi
21                        Overexpression of the helix-loop-helix motif-containing transcription inhibito
22 expectedly, the predicted leucine zipper and helix-loop-helix motifs do not form these structures but
23 M) domains, each containing two Ca2+ binding helix-loop-helix motifs (EF-hands), we revealed the key
24                    Mutation of the divergent helix-loop-helix motif found in 28-kDa HEF1 significantl
25   However, these data do not distinguish the helix-loop-helix motif from a continuous helix, because
26 -repeats, R1-R6, each containing a potential helix-loop-helix motif implicated in protein-protein int
27 potent neutralizing antibody that binds to a helix-loop-helix motif in the RSV fusion glycoprotein.
28 rane alpha-helix is reversibly formed from a helix-loop-helix motif in the solution structure.
29 rts the first two helices and the associated helix-loop-helix motif into a continuous alpha-helix, as
30 tic granulysin-derived peptides possessing a helix-loop-helix motif killed P. acnes in vitro.
31 and Ser(338) may also function with a nearby helix-loop-helix motif located at residues 339-372 to en
32 d through their leucine zipper motifs, their helix-loop-helix motifs may be involved in interactions
33                       The examination of the helix-loop-helix motif observed in the core protein stru
34 ctions between tRNA phosphate groups and the helix-loop-helix motif of HCMV pp150.
35                     A tight beta-turn in the helix-loop-helix motif of the cap domain contains a stri
36 onpolar residues that have been conserved in helix-loop-helix motifs of other proteins.
37 predicted zinc finger domain, and a putative helix-loop-helix motif, respectively, while the fourth c
38 yme, a small catalytic RNA consisting of two helix-loop-helix motifs, serves as a paradigm for RNA fo
39 ture of gp6 reveals a dimeric protein with a helix-loop-helix motif similar to that of bacteriophage
40 domain of P22 scaffolding protein exhibits a helix-loop-helix motif stabilized by a hydrophobic core.
41 her b(5) family members, Ncb5or-b(5) has two helix-loop-helix motifs surrounding heme.
42                                The DBD has a helix-loop-helix motif that is predicted to bind DNA.
43 c core domain and C-terminal domain adopts a helix-loop-helix motif that is similar to the correspond
44 igned to capture the conformation of the Sos helix-loop-helix motif that makes critical contacts with
45                                     The pore helix/loop/helix motifs that are contributed by three su
46 ith the first transmembrane domain forming a helix-loop-helix motif within the bilayer.