首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Extraordinary pleiotropy of protein kinase CK2 revealed by weblogo phosphoproteome analysis.
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Extraordinary pleiotropy of protein kinase CK2 revealed by weblogo phosphoproteome analysis.

机译:通过weblogo磷酸化蛋白质组分析揭示了蛋白激酶CK2的非同质性。

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摘要

A weblogo has been generated from the sequences surrounding 433 Ser/Thr protein residues whose phosphorylation by protein kinase CK2 had been previously validated ("bona fide" CK2 phosphosites). This has been compared to the weblogo extracted from 2275 putative CK2 phosphosites displaying the motif pS/pT-x1-x2-D/E/pS (where x1 not=P) present in the human phosphoElm database including 10899 naturally occurring phosphosites. The two weblogos are strikingly similar supporting the notion that indeed the 2275 putative sites (accounting for 20.9% of the whole phosphoproteome they belong to), or at least the great majority of these are generated by CK2. This conclusion has been corroborated by the random validation of 8 of such putative CK2 sites (belonging to 5 different proteins) as real targets of CK2 in vitro and/or in cells, leading to the inclusion into the repertoire of bona fide CK2 targets of 5 new entries, namely: oxidative stress-responsive kinase-1, anthrax toxin receptor 1, hepatoma derived growth factor, EpsinR and BCL2/adenovirus E1B 19 kDa protein-interacting protein 3-like.
机译:从围绕433个Ser / Thr蛋白残基的序列产生了一个Web徽标,该序列先前已被蛋白激酶CK2磷酸化(“真正的” CK2磷酸位点)。这已与从2275个推定的CK2磷酸位点提取的weblogo进行了比较,其中显示了包含在人类phosphoElm数据库中的基序pS / pT-x1-x2-D / E / pS(其中x1不是= P),其中包括10899个天然磷酸位点。这两个网页徽标非常相似,支持以下观点:确实有2275个推定位点(占它们所属的整个磷酸化蛋白质组的20.9%),或者至少其中大部分是由CK2产生的。通过在体外和/或细胞中随机验证8个这样的推定CK2位点(属于5种不同的蛋白质)作为CK2的真实靶标,从而证实了这一结论,从而将5个真正的CK2靶标包括在库中新条目,即:氧化应激反应激酶1,炭疽毒素受体1,肝癌衍生的生长因子,EpsinR和BCL2 /腺病毒E1B 19 kDa蛋白相互作用蛋白3-like。

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