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Molecular details of cAMP generation in mammalian cells: A tale of two systems

期刊

JOURNAL OF MOLECULAR BIOLOGY
卷 362, 期 4, 页码 623-639

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2006.07.045

关键词

cAMP signaling; class III nucleoticlyl cyclases; enzyme regulation; soluble adenylyl cyclases; transmembrane adenylyl cyclases

资金

  1. NIAID NIH HHS [AI64842, R01 AI064842] Funding Source: Medline
  2. NICHD NIH HHS [HD42060, R01 HD038722, HD38722] Funding Source: Medline
  3. NIDA NIH HHS [T32 DA007274, DA007274] Funding Source: Medline
  4. NIGMS NIH HHS [T32 GM073546, R01 GM062328, GM62328] Funding Source: Medline

向作者/读者索取更多资源

The second messenger cAMP has been extensively studied for half century but the plethora of regulatory mechanisms controlling cAMP synthesis in mammalian cells is just beginning to be revealed. mammalian cells, cAMP is produced by two evolutionary related families of adenylyl cyclases, soluble adenylyl cyclases (sAC) and transmembrane adenylyl cyclases (tmAC). These two enzyme families serve distinct physiological functions. They share a conserved overall architecture in their catalytic domains and a common catalytic mechanism, but they differ their sub-cellular localizations and responses to various regulators. The major regulators of tmACs are heterotrimeric G proteins, which transduce extracellular signals via G protein-coupled receptors. sAC enzymes, in contrast, are regulated by the intracellular signaling molecules bicarbonate and calcium. Here, we discuss and compare the biochemical, structural and regulatory characteristics of the two mammalian AC families. This comparison reveals the mechanisms underlying their different properties but also illustrates many unifying themes for these evolutionary related signaling enzymes. (c) 2006 Elsevier Ltd. All rights reserved.

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