None of the remaining Bm genomes encoded for this region.
Within higher plants, ∼7%; of their genomes encodes for putative TFs.
Avian, amphibian and teleost genomes encode for most of the mammalian orthologues, as well as additional TLRs [ 4- 6].
Mitochondrial genomes encode for the three distinct gene classes involved in this process: ribosomal, transfer, and protein-coding genes.
The CIAT 899 and PRF 81 genomes encoded for two MsrA and one MsrB methionine sulfoxide reductase repair-proteins [ 219].
Thus, these symbiont genomes encode for many of the metabolic pathways of free-living chemoautotrophs despite being reduced in size.
As stated in an earlier section, both genomes encode for two GH48 enzymes – one cellulosomal and another non-cellulosomal.
Plant closterovirus genomes encode for a homologue of cellular molecular chaperone HSP70 (Dolja et al. 2006) that is required for virion assembly (Satyanarayana et al. 2000).
The CIAT 899 and PRF 81 genomes encoded for a large conductance mechanosensitive channel MscL, and five and four small conductance mechanosensitive channels MscS, respectively.
Plant genomes encode for a high number of ABC proteins with more than 120 found in both Arabidopsis thaliana and Oryza sativa [ 8, 9].
