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Exact(6)
The cyclic segment of U-II peptide, CFWKYC, was the minimal sequence required for binding, with the WKY residues essential.
Structure activity relationship studies have shown that the minimal sequence required to retain full biological activity is the conserved U-II(4 11) domain, in particular the Cys5 and Cys10 residues involved in the disulfide bridge, and the Phe6, Lys8 and Tyr9 residues.
Previous studies have shown that the INNIXW motif is the minimal sequence required for peptide activity.
They also determined that the minimal sequence required for binding between the DLG motif and the Kelch domain is Ac-WRGDIDL-OH (Fig. 5).
The MKKK sequence is essential for the internalization by raft-dependent endocytosis [ 99] and the RMKKK motif is the minimal sequence required for its nuclear localization [ 100].
They determined that the minimal sequence required for binding between the ETGE motif and the Kelch domain is the seven-amino-acid sequence Ac-DEETGEF-OH and that the optimal sequence was Ac-DPETGEL-OH.
Similar(54)
TRIMs of plants and ants are presumed to be the result of convergent reductive evolution from autonomous elements, retaining only the minimal sequences required to efficiently complete the retrotransposition cycle (Schulman 2012).
The minimal protein sequence required for specific and high affinity RNA binding is a ∼73 residue segment that bears no sequence homology to any other protein in the eukaryotic genome.
Additionally, based on previous works, the minimal promoter sequence required for Synechocystis psbA2 basal transcription (−38 to +14 bp (base-pairs); +1 corresponding to the transcription start site) was synthesized (P psbA2*), meeting the BioBrick RFC[10] standard specifications (DNA 2.0 Inc).
DOI: http://dx.doi.org/10.7554/eLife.04132.011 To assess, as suggested by the time-lapse, whether Sec bodies form at ERES, we used a truncated version of Sec16, miniSec16 (690-1954), which comprises the minimal Sec16 sequence required for ERES localization (Ivan et al., 2008) but is not incorporated into Sec bodies upon amino-acid starvation.
For determination of the minimal promoter sequence required for p53 repression, 1.5 million CTB per well were plated in 12-well plates for 24 h and transfected with 3 µg of −670, −531 or –90 hMMP-9 promoter/CAT reporter plasmid and 0.5 µg wt-p53 or control vector.
Related(20)
minimal sequence needed
minimal sequence necessary
minimal intensity required
minimal sequence generated
minimal addition required
minimal current required
minimal sniggering required
minimal change required
minimal verification required
minimal work required
minimal equipment required
minimal accounting required
minimal surgery required
minimal skill required
minimal support required
minimal epitope required
minimal sensitivity required
minimal cleanup required
minimal system required
minimal distance required
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