Exact(29)
Most of the amplified marine sequences of this study exhibited low identities with known WS/DGAT enzymes and showed no close relatives, suggesting the phylogenetic diversity and novelty of these genes.
Most sequences had low identities with known xylanases in GenBank, implying that these xylanases may be as yet undiscovered.
Fifty-two distinct GH 10 and 35 GH 11 xylanase gene fragments (similarity <95%) were retrieved, and most had low identities with known sequences.
Proteins with high identities (>40%) are referred to as SMU.440 close homologs and those with low identities (<26%) are referred to as SMU.440 remote homologs.
The N. limnia AMO gene sequences have relatively low identities to N. maritimus, ranging from 80 91% nucleotide identity and 77 96% amino acid identity [Table 5].
Sequence analysis showed that most of the xylanase gene fragments have low identities to known xylanases, suggesting the existence of a large number of uncharacterized xylanase genes in rumen.
Similar(31)
Alignments with low identity (<30% identical sites), short length (<30 residues), or 100% identity were not included in the concatenation.
The sequences nearly identical to the query protein (sequence identity > 90%) or with a low identity (sequence identity < 30%) were excluded from the input data.
The ciliary genes identified showed low identity scores—< 51.5% between serotypes.
These loops bear a remarkable low identity though with high occurrence of ionizable residues, including histidines.
This low identity encourages its use for the design of new drugs against cysticercosis.
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