Linder Jürgen U, Schultz Joachim E
Fakultät fur Chemie und Pharmazie, Abteilung Pharmazeutische Biochemie, Pharmazeutisches Institut, Universität Tübingen, Morgenstelle 8, D-72076, Tübingen, Germany.
Cell Signal. 2003 Dec;15(12):1081-9. doi: 10.1016/s0898-6568(03)00130-x.
cAMP serves as a second messenger in virtually all organisms. The most wide-spread class of cAMP-generating enzymes are the class III adenylyl cyclases. Most class III adenylyl cyclases are multi-domain proteins. The catalytic domains exclusively work as dimers, catalysis proceeds at the dimer interface, so that both monomers provide catalytic residues to each catalytic center. Inspection of amino acid sequence profiles suggests a division of the class III adenylyl cyclases in to four subclasses, class IIIa-IIId. Genome projects and postgenomic analysis have provided novel aspects in terms of catalysis and regulation. Alterations in the canonical catalytic residues occur in all four subclasses suggesting a plasticity of the catalytic mechanisms. The vast variety of additional, probably regulatory modules found in class III adenylyl cyclases obviously reflects a large collection of regulatory inputs the catalytic domains have adapted to. The large versatility of class III adenylyl cyclase catalytic domains remains a major scientific challenge.
环磷酸腺苷(cAMP)几乎在所有生物体中都作为第二信使发挥作用。最广泛存在的一类产生cAMP的酶是III类腺苷酸环化酶。大多数III类腺苷酸环化酶是多结构域蛋白。催化结构域仅以二聚体形式起作用,催化作用在二聚体界面进行,因此两个单体都为每个催化中心提供催化残基。对氨基酸序列图谱的检查表明,III类腺苷酸环化酶可分为四个亚类,即IIIa - IIId。基因组计划和后基因组分析在催化和调控方面提供了新的视角。所有四个亚类中都出现了典型催化残基的改变,这表明催化机制具有可塑性。在III类腺苷酸环化酶中发现的大量额外的、可能具有调控作用的模块,显然反映了催化结构域所适应的大量调控输入。III类腺苷酸环化酶催化结构域的高度多功能性仍然是一个重大的科学挑战。