Houts G E, Miyagi M, Ellis C, Beard D, Watson K F, Beard J W
J Virol. 1978 Feb;25(2):546-52. doi: 10.1128/JVI.25.2.546-552.1978.
A protein kinase associated with purified virions of avian myeloblastosis BAI strain A was partially purified by ion-exchange chromatography and gel filtration. The transfer of phosphate catalyzed by this enzyme required a divalent metal ion and ATP as phosphate donor. GTP could not be substituted for ATP, and the reaction was unaffected by either cyclic AMP or beef-heart protein-kinase inhibitor. Of the virus and nonvirus proteins tested as phosphate acceptors, only acidic proteins were phosphorylated. In particular, purified preparations of reverse transcriptase from avian myeloblastosis virus did not accept phosphate. The enzyme is a basic protein (pI = 9.3), and, on the basis of molecular sieving through Sephadex G-200 and velocity sedimentation on glycerol gradient, the protein kinase has a molecular weight of 45,000.
通过离子交换色谱法和凝胶过滤法对与禽成髓细胞瘤BAI A株纯化病毒粒子相关的一种蛋白激酶进行了部分纯化。该酶催化的磷酸转移反应需要二价金属离子和ATP作为磷酸供体。GTP不能替代ATP,且该反应不受环磷酸腺苷或牛心蛋白激酶抑制剂的影响。在作为磷酸受体测试的病毒和非病毒蛋白中,只有酸性蛋白被磷酸化。特别是,来自禽成髓细胞瘤病毒的纯化逆转录酶制剂不接受磷酸。该酶是一种碱性蛋白(等电点 = 9.3),基于通过葡聚糖G - 200的分子筛和在甘油梯度上的速度沉降,该蛋白激酶的分子量为45,000。