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Multiple alignments revealed that Cys44 is conserved in all analysed Prx VI sequences.
Our multiple alignments revealed several conserved nucleotide positions at the 5' end of the COI gene.
Multiple alignments revealed the conservation of the Vps55 domain among lepr-encoded proteins.
Multiple alignments revealed that they share 28.7 56.8% DNA sequence identity with other members of Parvovirinae.
Multiple alignments revealed that PBoV1 and PBoV2 share 28.7 55.6% and 30.2 56.8% DNA sequence identity with other members of the subfamily Parvovirinae, respectively.
Finally, multiple alignments revealed the presence in most candidates of a conserved region near the C-terminus (Ser-Tyr-Ser or Ser-Tyr-Thr) also found in ORs from other dipteran species [8].
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Our whole genome multiple alignments reveal unannotated stretches of conservation in noncoding regions including transcription factor binding sites in promoter regions, noncoding RNAs, and mis-annotated proteins.
Interestingly, multiple alignments reveal that all class I enzymes from reptiles to humans, as well as other classes derived from amniote ADH1, such as ADH4 and ADH6, show a deletion at position 60 with respect to amphibian ADH1 proteins and the remaining ADH classes (see Additional file 15).
Interestingly, multiple alignment revealed a highly conserved signal peptide sequence, suggesting a common evolutionary origin for the three peptides.
Examination of its multiple alignment revealed a conserved NC-H-DxQ signature, which is reminiscent of the conservation pattern seen in papain-like peptidases [ 53, 71, 72].
Examination of a multiple alignment revealed that although M. smegmatis Mas1B does not actually have the N-terminal signature RD residues, the Cluster IIB proteins do.
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