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Various isoforms of histone proteins along with other nucleic acid binding proteins were also detected.
Other than uncharacterized proteins, genes encoding putative short chain dehydrogenases and periplasmic binding proteins were also among the most prevalent functions for proteins with predicted Tat signal sequences.
Interestingly, all microcystin binding proteins were also found to be differentially expressed in the previously performed proteomic study (Table 1) indicating that microcystin binding to proteins may at least partly explain the differences in the abundance of these proteins.
In addition, transcripts encoding nucleic acid binding and DNA binding proteins were also significantly enriched.
The insulin-like growth factor binding proteins were also significantly altered by senescence, including IGFBP2, IGFBP3, IGFBP5, and IGFBP6.
Several isoforms of Chlorophyll a/b binding protein and Chlorophyll a/c binding proteins were also identified (Table 1).
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Mechanisms that regulate PKC activity, including phosphorylation and interaction with isozyme-specific binding proteins, are also potential therapeutic targets.
It is highly likely, however, that the ability to cross-link other DNA binding proteins is also limited by the intrinsic temporal constraints on crosslink chemistry.
Lipid binding proteins are also involved in pollen-pistil interactions.
One of these sequences coding for odorant binding proteins was also found in BmPG (EZ407200).
Rho-GDI, ERK2 and the overall expression of P-GTP binding proteins is also enhanced in tumours, yet to a clearly lower level than Rho proteins are.
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