| Literature DB >> 25286305 |
Abstract
Multifunctional proteins provide a new mechanism to expand exponentially cell information and capability beyond that indicated by conventional gene analyses. As such, examination of their structure-function relationships provides a means to define the mechanisms through which cells accomplish critical yet disparate activities required for cell viability and survival. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) may be considered the quintessential multidimensional protein which exhibits a variety of functions unrelated to its classical role in energy production. This review discusses new insights into the structure-function mechanisms through which defined GAPDH amino acid domains are utilized for its diverse activities, the importance of its post-translational modification, and, intriguingly, the logic inherent in the presence or the absence of specific signaling domains.Entities:
Keywords: Amino acid domains; Glyceraldehyde-3-phosphate dehydrogenase; Multifunctional protein; Post-translational modification; mRNA stability
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Year: 2014 PMID: 25286305 PMCID: PMC4268148 DOI: 10.1016/j.biocel.2014.09.026
Source DB: PubMed Journal: Int J Biochem Cell Biol ISSN: 1357-2725 Impact factor: 5.085