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Each item of the sequence was displayed for 1500 ms and was followed by an inter-stimulus-interval of 400 ms. Sequences were predefined and pseudo-randomised.
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For each protein substrate, the sequence is displayed showing where cleavage occurs and which peptidase performs that cleavage.
In the case of protein sequences that are present in several databases, all protein IDs of the sequence are displayed in one line.
The sequence is displayed by two primers in both directions confirming point heteroplasmy of the variants A and G at position 2673 within the NADH dehydrogenase (ND2) gene.
The sequence is displayed from the N-terminus to the C-terminus by default; however, the order of the residues can be manipulated or reversed in the case of cyclic peptides.
The sequences were displayed in random order.
The clusters of proteins are listed and the sequences are displayed using the unique identifiers that were assigned by the prediction algorithms.
The homology between segments of the chimeric sequence was displayed using the ACT software [ 86].
The numeric sequence was displayed at the top of the screen to reduce the contribution of working memory on performance.
Spectra for OG or Gh at the same position gave nearly identical spectra, and therefore, only spectra for the OG-containing strands vs the WT sequence are displayed in the text for brevity (see Figure S6 for Gh-containing G4 CD spectra).
Domains that partially overlap and extend for more than 30 amino acids outside the signal sequence are displayed after the signal sequence.
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