Literature DB >> 16983687

Acetyl-coenzyme A carboxylases: versatile targets for drug discovery.

Liang Tong1, H James Harwood.   

Abstract

Acetyl-coenzyme A carboxylases (ACCs) have crucial roles in fatty acid metabolism in humans and most other living organisms. They are attractive targets for drug discovery against a variety of human diseases, including diabetes, obesity, cancer, and microbial infections. In addition, ACCs from grasses are the targets of herbicides that have been in commercial use for more than 20 years. Significant progresses in both basic research and in drug discovery have been made over the past few years in the studies on these enzymes. At the basic research level, the crystal structures of the biotin carboxylase (BC) and the carboxyltransferase (CT) components of ACC have been determined, and the molecular basis for ACC inhibition by small molecules are beginning to be understood. At the drug discovery level, a large number of nanomolar inhibitors of mammalian ACCs have been reported and the extent of their therapeutic potential is being aggressively explored. This review summarizes these new progresses and also offers some prospects in terms of the future directions for the studies on these important enzymes. (c) 2006 Wiley-Liss, Inc.

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Year:  2006        PMID: 16983687      PMCID: PMC3837461          DOI: 10.1002/jcb.21077

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  38 in total

1.  Function of Escherichia coli biotin carboxylase requires catalytic activity of both subunits of the homodimer.

Authors:  K Janiyani; T Bordelon; G L Waldrop; J E Cronan
Journal:  J Biol Chem       Date:  2001-06-04       Impact factor: 5.157

2.  Crystal structure of the carboxyltransferase domain of acetyl-coenzyme A carboxylase.

Authors:  Hailong Zhang; Zhiru Yang; Yang Shen; Liang Tong
Journal:  Science       Date:  2003-03-28       Impact factor: 47.728

3.  Potential mechanisms and consequences of cardiac triacylglycerol accumulation in insulin-resistant rats.

Authors:  Laura L Atkinson; Ray Kozak; Sandra E Kelly; Arzu Onay Besikci; James C Russell; Gary D Lopaschuk
Journal:  Am J Physiol Endocrinol Metab       Date:  2002-12-03       Impact factor: 4.310

4.  Molecular basis for the inhibition of the carboxyltransferase domain of acetyl-coenzyme-A carboxylase by haloxyfop and diclofop.

Authors:  Hailong Zhang; Benjamin Tweel; Liang Tong
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-12       Impact factor: 11.205

5.  Is dimerization required for the catalytic activity of bacterial biotin carboxylase?

Authors:  Yang Shen; Chi-Yuan Chou; Gu-Gang Chang; Liang Tong
Journal:  Mol Cell       Date:  2006-06-23       Impact factor: 17.970

Review 6.  AMP-activated protein kinase (AMPK) control of fatty acid and glucose metabolism in the ischemic heart.

Authors:  Nandakumar Sambandam; Gary D Lopaschuk
Journal:  Prog Lipid Res       Date:  2003-05       Impact factor: 16.195

7.  A bisubstrate analog inhibitor of the carboxyltransferase component of acetyl-CoA carboxylase.

Authors:  Keith L Levert; Grover L Waldrop
Journal:  Biochem Biophys Res Commun       Date:  2002-03-15       Impact factor: 3.575

8.  The subcellular localization of acetyl-CoA carboxylase 2.

Authors:  L Abu-Elheiga; W R Brinkley; L Zhong; S S Chirala; G Woldegiorgis; S J Wakil
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-15       Impact factor: 11.205

9.  Continuous fatty acid oxidation and reduced fat storage in mice lacking acetyl-CoA carboxylase 2.

Authors:  L Abu-Elheiga; M M Matzuk; K A Abo-Hashema; S J Wakil
Journal:  Science       Date:  2001-03-30       Impact factor: 47.728

10.  Expression and characterization of recombinant fungal acetyl-CoA carboxylase and isolation of a soraphen-binding domain.

Authors:  Stephanie C Weatherly; Sandra L Volrath; Tedd D Elich
Journal:  Biochem J       Date:  2004-05-15       Impact factor: 3.857

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  70 in total

1.  Mechanism for the inhibition of the carboxyltransferase domain of acetyl-coenzyme A carboxylase by pinoxaden.

Authors:  Linda P C Yu; Yi Seul Kim; Liang Tong
Journal:  Proc Natl Acad Sci U S A       Date:  2010-12-06       Impact factor: 11.205

2.  Soraphen A, an inhibitor of acetyl CoA carboxylase activity, interferes with fatty acid elongation.

Authors:  Donald B Jump; Moises Torres-Gonzalez; L Karl Olson
Journal:  Biochem Pharmacol       Date:  2010-12-22       Impact factor: 5.858

3.  Emerging Pharmacological Targets for the Treatment of Nonalcoholic Fatty Liver Disease, Insulin Resistance, and Type 2 Diabetes.

Authors:  Leigh Goedeke; Rachel J Perry; Gerald I Shulman
Journal:  Annu Rev Pharmacol Toxicol       Date:  2019-01-06       Impact factor: 13.820

4.  Targeting stearoyl-CoA desaturase 1 to repress endometrial cancer progression.

Authors:  Weihua Li; Huimin Bai; Shiping Liu; Dongyan Cao; Hongying Wu; Keng Shen; Yanhong Tai; Jiaxin Yang
Journal:  Oncotarget       Date:  2018-01-24

5.  COP1 functions as a FoxO1 ubiquitin E3 ligase to regulate FoxO1-mediated gene expression.

Authors:  Satomi Kato; Jixin Ding; Evan Pisck; Ulupi S Jhala; Keyong Du
Journal:  J Biol Chem       Date:  2008-09-24       Impact factor: 5.157

6.  Chronic suppression of acetyl-CoA carboxylase 1 in beta-cells impairs insulin secretion via inhibition of glucose rather than lipid metabolism.

Authors:  Sarah M Ronnebaum; Jamie W Joseph; Olga Ilkayeva; Shawn C Burgess; Danhong Lu; Thomas C Becker; A Dean Sherry; Christopher B Newgard
Journal:  J Biol Chem       Date:  2008-04-01       Impact factor: 5.157

7.  Systems-level metabolic flux profiling identifies fatty acid synthesis as a target for antiviral therapy.

Authors:  Joshua Munger; Bryson D Bennett; Anuraag Parikh; Xiao-Jiang Feng; Jessica McArdle; Herschel A Rabitz; Thomas Shenk; Joshua D Rabinowitz
Journal:  Nat Biotechnol       Date:  2008-09-28       Impact factor: 54.908

8.  Crystal structure of biotin carboxylase in complex with substrates and implications for its catalytic mechanism.

Authors:  Chi-Yuan Chou; Linda P C Yu; Liang Tong
Journal:  J Biol Chem       Date:  2009-02-12       Impact factor: 5.157

9.  Identifying essential genes in bacterial metabolic networks with machine learning methods.

Authors:  Kitiporn Plaimas; Roland Eils; Rainer König
Journal:  BMC Syst Biol       Date:  2010-05-03

10.  Acetyl-CoA carboxylase inhibition by ND-630 reduces hepatic steatosis, improves insulin sensitivity, and modulates dyslipidemia in rats.

Authors:  Geraldine Harriman; Jeremy Greenwood; Sathesh Bhat; Xinyi Huang; Ruiying Wang; Debamita Paul; Liang Tong; Asish K Saha; William F Westlin; Rosana Kapeller; H James Harwood
Journal:  Proc Natl Acad Sci U S A       Date:  2016-03-14       Impact factor: 11.205

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