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Cellular function of each TF binding motif was also inferred from the GO terms enriched in their target genes.

The interaction topology between a domain and the binding motif was also roughly conserved, with all motifs placed in the same binding groove.

In addition, a metal binding motif shared by many E1-like enzymes such as human Uba5, Uba2, Uba3, Uba4 and Atg7 and an active site Cys residue occurring downstream of the metal binding motif was also found in trypanosomatid Uba5 (Figure S2).

A HEXXH binding motif was also identified within this collagenase sequence.

A binding motif was also found for GATA1 protein (error type I -0,1111, error type II -0,00451, psum -90,1055) (Fig. 3B).

Now in the current study PIK3C2G possessing the C2 domain acting as lipid binding motif was also implicated in eggshell property.

The activated ncRNA loci containing a putative CEP-1 binding motif were also unevenly distributed on the chromosomes in that approximately 50% of these ncRNAs were enriched on chromosomes V and X.

Several peptides with mutation within the PDZ binding motif were also included in the ELISA-based affinity study.

The improvement in the definition of the binding motif is also visible in the logos for the two transcription factors.

Interestingly, the Fe S-binding motiFe S-bindingbserved in both groups F and G.

Unique potential binding motifs were also identified in the promoter region of miR-433 and of miR-127 in each species.