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The two other CDSs, Ccar_0005 and Ccar_0017, were both predicted to encode a NADH-dependent butanol dehydrogenase responsible for the conversion of butyraldehyde to butanol.
Novel subtypes, stG6.5 and stG6.7, were found in 2 GGS isolates, both predicted to encode truncated M proteins of only 56 and 42 residues respectively.
Twenty-five genes are annotated in this region of the peach genome (Table 3) and we focused our attention on ppa007577m and ppa008301m, both predicted to encode NAC transcription factors (TFs).
Genes actA and actB, both predicted to encode response regulators of the two-component signal transduction family whose function thus far is proposed to be regulation of the level of CsgA (a key regulator of the aggregation and sporulation in the starvation-induced developmental program) [ 37], were upregulated in our microarray data.
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Similarly, two different MYB29 mRNA sequences exist one of 1595 bp (NM_120851) and one of 1292 bp (AF062872)–both are predicted to encode a 337 aa protein.
Both are predicted to encode helix-loop-helix TFs with unknown function in Arabidopsis.
C. cellulolyticum has two paralogs of the ldh gene that were both originally predicted to encode L-lactate dehydrogenase (LDH) enzymes: Ccel_0137 and Ccel_2485.
Interestingly, both genomes are predicted to encode a high number of GHs that belong to the GH family 43.
Both genes are predicted to encode secretory proteins that are specifically expressed in the heads of female neotenics.
A gene (Cthe_0271) was highly expressed on both biomasses and is predicted to encode a protein with a putative function as a type 3A cellulose-binding protein.
There are at least two other predicted EF-Gs in the Arabidopsis genome, both of which are predicted to encode EF-Gs with mitochondrial-targeting and possibly plastid-targeting sequences.
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