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From Protein Structure to Function with Bioinformatics.pdf

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6 <strong>Function</strong> Diversity Within Folds and Superfamilies 161Figure 6.4 summarises the functional diversity in that superfamily, <strong>to</strong>gether <strong>with</strong>representative structures for the main functional groups. Yet, due <strong>to</strong> the difficulty<strong>to</strong> apprehend function, it may well be that even <strong>with</strong>in these extremely diversesuperfamilies, functional commonalities that are not apparent at this stage willcome <strong>to</strong> light as more data is collected and studied.6.3.3.2 <strong>Function</strong> Diversity Between Close HomologuesThe above sections described the amount of functional diversity that is <strong>to</strong> beexpected <strong>with</strong>in protein superfamilies, <strong>with</strong> particular emphasis on remote homologues.But functional diversity is also observed between closer homologues (e.g.Fig. 6.4 Diversity of structures and functions in the HUP-domains superfamily (CATH code3.40.50.620). HUP-domains adopt a Rossmann-like fold and have been shown <strong>to</strong> be very ancient(Aravind et al. 2002). Together, they form a very large superfamily <strong>with</strong> many different functions.In this figure, representative structures of the major functional groups in this superfamily aredisplayed in car<strong>to</strong>ons. These structures were multiply aligned <strong>with</strong> CORA (Orengo 1999) and themultiple alignment was used <strong>to</strong> derive the common core of the domain. Residues that constitutethe core are coloured red in each structure. The CATH domains that were used as representativesof each functional groups are: (a) 1dnpA01 for DNA repair pho<strong>to</strong>lyases, (b) 1ej2A00 for nucleotidyltransferases,(c) 1gpmA02 for N-type ATP pyrophosphatases, (d) 1n3lA01 for class I aminoacyltRNA synthetases and (e) 1o97D01 for electron transfer flavoproteins

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