Phosphatidylinositol kinases in GtoPdb v.2023.1

Mohib Uddin
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Abstract

Phosphatidylinositol may be phosphorylated at either 3- or 4- positions on the inositol ring by PI 3-kinases or PI 4-kinases, respectively.Phosphatidylinositol 3-kinasesPhosphatidylinositol 3-kinases (PI3K, provisional nomenclature) catalyse the introduction of a phosphate into the 3-position of phosphatidylinositol (PI), phosphatidylinositol 4-phosphate (PIP) or phosphatidylinositol 4,5-bisphosphate (PIP2). There is evidence that PI3K can also phosphorylate serine/threonine residues on proteins. In addition to the classes described below, further serine/threonine protein kinases, including ATM (Q13315) and mTOR (P42345), have been described to phosphorylate phosphatidylinositol and have been termed PI3K-related kinases. Structurally, PI3Ks have common motifs of at least one C2, calcium-binding domain and helical domains, alongside structurally-conserved catalytic domains. wortmannin and LY 294002 are widely-used inhibitors of PI3K activities. wortmannin is irreversible and shows modest selectivity between Class I and Class II PI3K, while LY294002 is reversible and selective for Class I compared to Class II PI3K.Class I PI3Ks (EC 2.7.1.153) phosphorylate phosphatidylinositol 4,5-bisphosphate to generate phosphatidylinositol 3,4,5-trisphosphate and are heterodimeric, matching catalytic and regulatory subunits. Class IA PI3Ks include p110α, p110β and p110δ catalytic subunits, with predominantly p85 and p55 regulatory subunits. The single catalytic subunit that forms Class IB PI3K is p110γ. Class IA PI3Ks are more associated with receptor tyrosine kinase pathways, while the Class IB PI3K is linked more with GPCR signalling.Class II PI3Ks (EC 2.7.1.154) phosphorylate phosphatidylinositol to generate phosphatidylinositol 3-phosphate (and possibly phosphatidylinositol 4-phosphate to generate phosphatidylinositol 3,4-bisphosphate). Three monomeric members exist, PI3K-C2α, β and β, and include Ras-binding, Phox homology and two C2 domains.The only class III PI3K isoform (EC 2.7.1.137) is a heterodimer formed of a catalytic subunit (VPS34) and regulatory subunit (VPS15).Phosphatidylinositol 4-kinasesPhosphatidylinositol 4-kinases (EC 2.7.1.67) generate phosphatidylinositol 4-phosphate and may be divided into higher molecular weight type III and lower molecular weight type II forms.
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GtoPdb v.2023.1中磷脂酰肌醇激酶
磷脂酰肌醇可能在肌醇环上的3位或4位分别被PI 3-激酶或PI 4-激酶磷酸化。磷脂酰肌醇3-激酶磷脂酰肌醇3-激酶(PI3K,临时命名)催化磷酸在磷脂酰肌醇(PI)、4-磷酸磷脂酰肌醇(PIP)或4,5-二磷酸磷脂酰肌醇(PIP2)的3位上引入磷酸。有证据表明,PI3K也可以磷酸化蛋白质上的丝氨酸/苏氨酸残基。除了下面描述的类别,其他丝氨酸/苏氨酸蛋白激酶,包括ATM (Q13315)和mTOR (P42345),已被描述为磷酸化磷脂酰肌醇,并被称为pi3k相关激酶。在结构上,pi3k具有至少一个C2、钙结合结构域和螺旋结构域的共同基序,以及结构保守的催化结构域。wortmannin和LY 294002是广泛使用的PI3K活性抑制剂。wortmannin是不可逆的,在I类和II类PI3K之间具有一定的选择性,而LY294002与II类PI3K相比,对I类PI3K具有可逆性和选择性。I类PI3K (EC 2.7.1.153)磷酸化磷脂酰肌醇4,5-二磷酸生成磷脂酰肌醇3,4,5-三磷酸,是异二聚体,与催化和调节亚基匹配。IA类pi3k包括p110α、p110β和p110δ催化亚基,主要是p85和p55调控亚基。形成IB类PI3K的单一催化亚基是p110γ。IA类PI3K更多地与受体酪氨酸激酶途径相关,而IB类PI3K更多地与GPCR信号通路相关。II类PI3K (EC 2.7.1.154)磷酸化磷脂酰肌醇生成3-磷酸磷脂酰肌醇(也可能磷酸化4-磷酸磷脂酰肌醇生成3,4-二磷酸磷脂酰肌醇)。PI3K-C2α、β和β三个单体成员包含Ras-binding、Phox同源性和两个C2结构域。唯一的III类PI3K异构体(EC 2.7.1.137)是由催化亚基(VPS34)和调节亚基(VPS15)组成的异源二聚体。磷脂酰肌醇4-激酶磷脂酰肌醇4-激酶(EC 2.7.1.67)产生磷酸磷脂酰肌醇,可分为高分子量III型和低分子量II型。
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