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This shows that gene families with ion and ATP or GTP binding functions are more likely to undergo heterogeneous rates of CNCs in multiple species.
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Based on analysis of the evolutionary history of agrin we suggest that agrin's growth factor binding function is more ancient than its involvement in acetylcholine receptor clustering.
Nucleic acid binding, protein binding, and ion binding functions were predominated in the binding category.
"Lullaby's" second function is more labored.
However, functions of GAGA-motif binding proteins are more diverse and can also be linked to epigenetic regulation of homeotic genes e.g. by recruiting silencing factors to specific sites, as well as influencing the promoter-proximal pausing of RNA Polymerase II (Pol II) [5], [9], [10], [11].
In contrast, GO terms related to the molecular functions cation binding and nucleotide binding are clearly more present within contigs, while GO terms related to the molecular functions protein binding, small molecule binding, hydrolase activity, ion binding, transferase activity and nucleic acid binding are more present within singletons.
Space-binding media are more ephemeral.
These binding sites were more conserved and located closer to TSSs than those whose function was not experimentally verified [18].
We suggest that agrin's biological function as a growth factor binding protein may be more ancient and more general than its involvement in synaptogenesis.
Stronger binding sites could be under higher selective pressure, since they are more likely to have a vital function.
The Ach-binding MfdA is mainly dependent on D34, while reserpine-binding site is more hydrophobic.
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