Adenylyl cyclases (ACs) in GtoPdb v.2023.1

C. Dessauer, R. Ostrom, R. Seifert, V. Watts
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Abstract

Adenylyl cyclase, E.C. 4.6.1.1, converts ATP to cyclic AMP and pyrophosphate. Mammalian membrane-delimited adenylyl cyclases (nomenclature as approved by the NC-IUPHAR Subcommittee on Adenylyl cyclases [11]) are typically made up of two clusters of six TM domains separating two intracellular, overlapping catalytic domains that are the target for the nonselective activators Gαs (the stimulatory G protein α subunit) and forskolin (except AC9, [28]). adenosine and its derivatives (e.g. 2',5'-dideoxyadenosine), acting through the P-site,are inhibitors of adenylyl cyclase activity [35]. Four families of membranous adenylyl cyclase are distinguishable: calmodulin-stimulated (AC1, AC3 and AC8), Ca2+- and Gβγ-inhibitable (AC5, AC6 and AC9), Gβγ-stimulated and Ca2+-insensitive (AC2, AC4 and AC7), and forskolin-insensitive (AC9) forms. A soluble adenylyl cyclase (AC10) lacks membrane spanning regions and is insensitive to G proteins.It functions as a cytoplasmic bicarbonate (pH-insensitive) sensor [7].
GtoPdb v.2023.1中的腺苷酸环化酶(ACs)
腺苷酸环化酶(E.C. 4.6.1.1)将ATP转化为环状AMP和焦磷酸。哺乳动物膜界腺苷酸环化酶(由NC-IUPHAR腺苷酸环化酶小组委员会批准的命名法[11])通常由两个由6个TM结构域组成的簇组成,这些结构域分离了两个细胞内重叠的催化结构域,它们是非选择性激活剂Gαs(刺激G蛋白α亚基)和forskolin (AC9除外,[28])的靶标。腺苷及其衍生物(如2',5'-二脱氧腺苷)通过p位点起作用,是腺苷酸环化酶活性的抑制剂[35]。膜腺苷酸环化酶可区分为四个家族:钙调素刺激型(AC1、AC3和AC8), Ca2+和g βγ抑制型(AC5、AC6和AC9), g βγ刺激型和Ca2+不敏感型(AC2、AC4和AC7), forskolin不敏感型(AC9)。可溶性腺苷酸环化酶(AC10)缺乏跨膜区,对G蛋白不敏感。它的功能是细胞质碳酸氢盐(ph不敏感)传感器[7]。
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