Intrinsic Disorder and Posttranslational Modifications: The Darker Side of the Biological Dark Matter

被引:172
作者
Darling, April L. [1 ]
Uversky, Vladimir N. [1 ,2 ]
机构
[1] Univ S Florida, Morsani Coll Med, USF Hlth Byrd Alzheimers Inst, Dept Mol Med, Tampa, FL 33620 USA
[2] Russian Acad Sci, Inst Biol Instrumentat, Lab New Methods Biol, Pushchino, Russia
基金
美国国家卫生研究院;
关键词
intrinsically disordered proteins; intrinsically disordered protein regions; posstranslational modifications; multifunctional proteins; protein-protein interaction (PPI); MOLECULAR RECOGNITION FEATURES; DEPENDENT PROTEIN-KINASE; NATIVELY UNFOLDED PROTEINS; UNSTRUCTURED PROTEINS; CRYSTAL-STRUCTURE; FUNCTIONAL ANTHOLOGY; CATALYTIC SUBUNIT; NEUROFIBRILLARY DEGENERATION; HISTONE MODIFICATIONS; CHANNEL INACTIVATION;
D O I
10.3389/fgene.2018.00158
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Intrinsically disordered proteins (IDPs) and intrinsically disordered protein regions (IDPRs) are functional proteins and domains that devoid stable secondary and/or tertiary structure. IDPs/IDPRs are abundantly present in various proteomes, where they are involved in regulation, signaling, and control, thereby serving as crucial regulators of various cellular processes. Various mechanisms are utilized to tightly regulate and modulate biological functions, structural properties, cellular levels, and localization of these important controllers. Among these regulatory mechanisms are precisely controlled degradation and different posttranslational modifications (PTMs). Many normal cellular processes are associated with the presence of the right amounts of precisely activated IDPs at right places and in right time. However, wrecked regulation of IDPs/IDPRs might be associated with various human maladies, ranging from cancer and neurodegeneration to cardiovascular disease and diabetes. Pathogenic transformations of IDPs/IDPRs are often triggered by altered PTMs. This review considers some of the aspects of IDPs/IDPRs and their normal and aberrant regulation by PTMs.
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页数:18
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