Literature DB >> 15952893

Structure and function of fatty acid amide hydrolase.

Michele K McKinney1, Benjamin F Cravatt.   

Abstract

Fatty acid amide hydrolase (FAAH) is a mammalian integral membrane enzyme that degrades the fatty acid amide family of endogenous signaling lipids, which includes the endogenous cannabinoid anandamide and the sleep-inducing substance oleamide. FAAH belongs to a large and diverse class of enzymes referred to as the amidase signature (AS) family. Investigations into the structure and function of FAAH, in combination with complementary studies of other AS enzymes, have engendered provocative molecular models to explain how this enzyme integrates into cell membranes and terminates fatty acid amide signaling in vivo. These studies, as well as their biological and therapeutic implications, are the subject of this review.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15952893     DOI: 10.1146/annurev.biochem.74.082803.133450

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


  217 in total

1.  N-acyl taurines are anti-proliferative in prostate cancer cells.

Authors:  Vicky Chatzakos; Katharina Slätis; Tatjana Djureinovic; Thomas Helleday; Mary C Hunt
Journal:  Lipids       Date:  2011-12-11       Impact factor: 1.880

2.  N-acylethanolamine (NAE) inhibits growth in Arabidopsis thaliana seedlings via ABI3-dependent and -independent pathways.

Authors:  Matthew Q Cotter; Neal D Teaster; Elison B Blancaflor; Kent D Chapman
Journal:  Plant Signal Behav       Date:  2011-05-01

3.  Moving bliss: a new anandamide transporter.

Authors:  Giovanni Marsicano; Francis Chaouloff
Journal:  Nat Neurosci       Date:  2011-12-23       Impact factor: 24.884

4.  The Central Role of Glia in Pathological Pain and the Potential of Targeting the Cannabinoid 2 Receptor for Pain Relief.

Authors:  Jenny L Wilkerson; Erin D Milligan
Journal:  ISRN Anesthesiol       Date:  2011

5.  Covalent inhibitors of fatty acid amide hydrolase: a rationale for the activity of piperidine and piperazine aryl ureas.

Authors:  Giulia Palermo; Davide Branduardi; Matteo Masetti; Alessio Lodola; Marco Mor; Daniele Piomelli; Andrea Cavalli; Marco De Vivo
Journal:  J Med Chem       Date:  2011-09-08       Impact factor: 7.446

6.  Strategies for discovering and derisking covalent, irreversible enzyme inhibitors.

Authors:  Douglas S Johnson; Eranthie Weerapana; Benjamin F Cravatt
Journal:  Future Med Chem       Date:  2010-06       Impact factor: 3.808

7.  N-Acylethanolamine metabolism interacts with abscisic acid signaling in Arabidopsis thaliana seedlings.

Authors:  Neal D Teaster; Christy M Motes; Yuhong Tang; William C Wiant; Matthew Q Cotter; Yuh-Shuh Wang; Aruna Kilaru; Barney J Venables; Karl H Hasenstein; Gabriel Gonzalez; Elison B Blancaflor; Kent D Chapman
Journal:  Plant Cell       Date:  2007-08-31       Impact factor: 11.277

Review 8.  Lipidomic analysis of endocannabinoid metabolism in biological samples.

Authors:  Giuseppe Astarita; Daniele Piomelli
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2009-01-14       Impact factor: 3.205

9.  Synthesis of phenoxyacyl-ethanolamides and their effects on fatty acid amide hydrolase activity.

Authors:  Lionel Faure; Subbiah Nagarajan; Hyeondo Hwang; Christa L Montgomery; Bibi Rafeiza Khan; George John; Peter Koulen; Elison B Blancaflor; Kent D Chapman
Journal:  J Biol Chem       Date:  2014-02-20       Impact factor: 5.157

10.  Isolation of a sleep-promoting compound from Polygonatum sibiricum rhizome.

Authors:  Kyungae Jo; Hoon Kim; Hyeon-Son Choi; Seung-Su Lee; Myun-Ho Bang; Hyung Joo Suh
Journal:  Food Sci Biotechnol       Date:  2018-07-13       Impact factor: 2.391

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.