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From Protein Structure to Function with Bioinformatics.pdf

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124 P. TompaTable 5.2 Classification scheme of IDPs. Classification of IDPs encompassing seven functionalcategories based on their molecular modes of action. Two examples <strong>with</strong>in each category are given,specifying the binding partner (if applicable) and the actual cellular function of the protein<strong>Protein</strong> Partner <strong>Function</strong>Entropic chainsNup2p FG repeat region n.a. Gating in NPCK channel N-terminal region n.a. Timing of gate inactivationDisplay sitesCREB KID PKA Phosphorylation siteCyclin B N-terminal domain E3 ubiquitin ligase Ubiquitination siteChaperonesERD 10/14 (e.g.) Luciferase Prevention of aggregationhnRNP A1 (e.g.) DNA Strand re-annealingEffec<strong>to</strong>rsp27Kip1 CycA-Cdk2 Inhibition of cell-cycleSecurin Separase Inhibition of anaphaseAssemblersRNAP II CTD mRNA maturation fac<strong>to</strong>rs Regulation of mRNA maturationCREB p300/CBP Initiation of transcriptionScavengersCasein Calcium phosphate Stabilization of calciumphosphate in milkSalivary PRPs Tannin Neutralization of plant tanninsPrionsUre2pUtilization of urea undernitrogenSup35p NusA, mRNA Suppression of s<strong>to</strong>p codon,translation readthroughbristles/spacers, linkers, and clocks, and the underlying mechanisms can be bestdescribed as either influencing the localization of attached domains, or generatingforce against movements/structural changes (Dunker et al. 2002). The best characterizedexamples in this category are entropic gating in nuclear pore complex bydisordered regions of NUPs (Elbaum 2006), the entropic spacer/bristle function ofprojection domains of microtubule-associated proteins in the cy<strong>to</strong>skele<strong>to</strong>n(Mukhopadhyay and Hoh 2001), and the entropic spring action of the PEVK regionof titin, ensuring passive tension in resting muscle due <strong>to</strong> its elasticity (Trombitaset al. 1998).5.4.2.2 <strong>Function</strong> by Transient BindingIn the other six categories, IDPs function via molecular recognition, i.e. they bindother macromolecule(s) or small ligand(s) either transiently or permanently.Display sites are primarily targeted for post-translational modifications. For example,

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