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Bauer et al. 74 tackled mutant Huntingtin protein in HD by designing a polyglutamine-binding peptide, fused to heat shock cognate protein 70 binding motif, such that it would promote degradation of aggregates by chaperone-mediated autophagy.
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Ala-scanning mutagenesis of each residue of the VMEFDPL stretch suggests that changing individual residue did not affect the interaction with clathrin (Supplementary Figure 5B), which is in marked contrast with canonical clathrin-binding motif such as that of Ack1 in that changing each residue of the clathrin box abolished interaction with clathrin (Teo et al, 2001).
Specifically, the interactions of trans-acting proteins with their cognate RNA binding motifs such as those that have been reported between the USE and stimulatory and inhibitory proteins of 3′end processing (Danckwardt et al, 2011) could, in principle, be envisaged to be targeted by small molecules thus modulating 3′end processing efficiency of specific classes of genes.
Genes for transcription factors that contain typical DNA binding motifs, such as MYB, bZIP, have been demonstrated to be stress inducible [ 24].
PI3K (III) is thought to exert its function through the recruitment of proteins that contain PI(3 P-binding motifs such as FYVE or PX domains [29], [3 P-binding
RBPs contain one or more RNA-binding motifs, such as hnRNP K homology motif, RNA recognition motif (RRM), RGG box, and dsRBD motif [ 5- 7].
This is even more apparent when looking at the functional classification of direct translation targets containing the SRSF1 consensus binding motif that includes several redundant layers such as cell cycle (p = 3.35E-06), chrorganizationnization (p = 2.79E-07), and M phase (p = 3.61E-05), suggesthat that SRSF1-mediated translation may affect proper mitotic progression.
To search for novel peptides and common binding motif that specifically bind to endometriosis.
The W-box is a binding motif that has been identified in WRKY transcription factors.
These motifs predict transcription-factor binding motifs that may control the expression of each cluster.
Henriksson, M. L. et al. A nonphosphorylated 14-3-3 14-3-3 14-3-3 on exoenzyme S that is functional in vivo.
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