Literature DB >> 27088879

The Substrate Specificity of Sirtuins.

Poonam Bheda1,2, Hui Jing3, Cynthia Wolberger4, Hening Lin3,5.   

Abstract

Sirtuins are NAD(+)-dependent enzymes universally present in all organisms, where they play central roles in regulating numerous biological processes. Although early studies showed that sirtuins deacetylated lysines in a reaction that consumes NAD(+), more recent studies have revealed that these enzymes can remove a variety of acyl-lysine modifications. The specificities for varied acyl modifications may thus underlie the distinct roles of the different sirtuins within a given organism. This review summarizes the structure, chemistry, and substrate specificity of sirtuins with a focus on how different sirtuins recognize distinct substrates and thus carry out specific functions.

Entities:  

Keywords:  ADP-ribosylation; deacylation; myristoylation; palmitoylation; succinylation

Mesh:

Substances:

Year:  2016        PMID: 27088879     DOI: 10.1146/annurev-biochem-060815-014537

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  79 in total

Review 1.  Location, Location, Location: Compartmentalization of NAD+ Synthesis and Functions in Mammalian Cells.

Authors:  Xiaolu A Cambronne; W Lee Kraus
Journal:  Trends Biochem Sci       Date:  2020-06-25       Impact factor: 13.807

2.  Entropy as a Driver of Selectivity for Inhibitor Binding to Histone Deacetylase 6.

Authors:  Nicholas J Porter; Florence F Wagner; David W Christianson
Journal:  Biochemistry       Date:  2018-05-18       Impact factor: 3.162

3.  Advances in the Development of Therapeutics for Cytomegalovirus Infections.

Authors:  Edward Acosta; Terry Bowlin; Jennifer Brooks; Lillian Chiang; Islam Hussein; David Kimberlin; Lawrence M Kauvar; Randi Leavitt; Mark Prichard; Richard Whitley
Journal:  J Infect Dis       Date:  2020-03-05       Impact factor: 5.226

4.  Binding of the Microbial Cyclic Tetrapeptide Trapoxin A to the Class I Histone Deacetylase HDAC8.

Authors:  Nicholas J Porter; David W Christianson
Journal:  ACS Chem Biol       Date:  2017-08-30       Impact factor: 5.100

5.  SIRT5 stabilizes mitochondrial glutaminase and supports breast cancer tumorigenesis.

Authors:  Kai Su Greene; Michael J Lukey; Xueying Wang; Bryant Blank; Joseph E Druso; Miao-Chong J Lin; Clint A Stalnecker; Chengliang Zhang; Yashira Negrón Abril; Jon W Erickson; Kristin F Wilson; Hening Lin; Robert S Weiss; Richard A Cerione
Journal:  Proc Natl Acad Sci U S A       Date:  2019-12-16       Impact factor: 11.205

Review 6.  Epigenetic regulation in cell senescence.

Authors:  Li-Qin Cheng; Zhu-Qin Zhang; Hou-Zao Chen; De-Pei Liu
Journal:  J Mol Med (Berl)       Date:  2017-09-08       Impact factor: 4.599

Review 7.  Epigenetic drug discovery: a success story for cofactor interference.

Authors:  A Ganesan
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2018-06-05       Impact factor: 6.237

8.  Molecular Imaging of Sirtuin1 Expression-Activity in Rat Brain Using Positron-Emission Tomography-Magnetic-Resonance Imaging with [18F]-2-Fluorobenzoylaminohexanoicanilide.

Authors:  Robin Bonomi; Vadim Popov; Maxwell T Laws; David Gelovani; Anjoy Majhi; Aleksandr Shavrin; Xin Lu; Otto Muzik; Nashaat Turkman; Renshyan Liu; Thomas Mangner; Juri G Gelovani
Journal:  J Med Chem       Date:  2018-08-13       Impact factor: 7.446

9.  Genetically Encoded Fluorescent Probe for Detecting Sirtuins in Living Cells.

Authors:  Weimin Xuan; Anzhi Yao; Peter G Schultz
Journal:  J Am Chem Soc       Date:  2017-08-31       Impact factor: 15.419

Review 10.  Chemical and Physiological Features of Mitochondrial Acylation.

Authors:  Alison E Ringel; Sarah A Tucker; Marcia C Haigis
Journal:  Mol Cell       Date:  2018-11-15       Impact factor: 17.970

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