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There are nine known adenylate cyclases in mammals:
cAMP is an important molecule in eukaryotic signal transduction, a so-called second messenger. Adenylate cyclase can be activated or inhibited by G proteins, which are coupled to membrane receptors and thus can respond to hormonal or other stimuli.
The important parts for its function are located in the cytoplasm and can be subdivided into the N-terminus, C1a, C1b, C2a and C2b.
The C1 region exists between transmembrane helices six and seven and the C2 region follows transmembrane helix 12.
The C1a and C2a domains form a catalytic dimer where ATP binds and is converted to cAMP.
Adenylate cyclase is stimulated by G proteins, and by forskolin, as well as other class-specific substrates:
- Isoforms I, III and VIII are also stimulated by Ca2+/calmodulin.
- Isoforms V and VI are inhibited by Ca2+ in a calmodulin-independent manner.
In neurons, adenylate cyclases are located next to calcium ion channels for faster reaction to Ca2+ influx; they are suspected of playing an important role in learning processes. This is supported by the fact that adenylate cyclases are coincidence detectors, meaning that they are only activated by several different signals occurring together.
Enzyme catalysis - Enzyme inhibitor - Enzyme kinetics - Lineweaver-Burk plot - Michaelis-Menten kinetics - List of enzymes
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