Eisenhaber Birgit, Eisenhaber Frank
Experimental Therapeutic Centre, Bioinformatics Institute, Agency for science, Technology, and Research, Singapore.
Methods Mol Biol. 2010;609:365-84. doi: 10.1007/978-1-60327-241-4_21.
If posttranslational modifications (PTMs) are chemical alterations of the protein primary structure during the protein's life cycle as a result of an enzymatic reaction, then the motif in the substrate protein sequence that is recognized by the enzyme can serve as basis for predictor construction that recognizes PTM sites in database sequences. The recognition motif consists generally of two regions: first, a small, central segment that enters the catalytic cleft of the enzyme and that is specific for this type of PTM and, second, a sequence environment of about 10 or more residues with linker characteristics (a trend for small and polar residues with flexible backbone) on either side of the central part that are needed to provide accessibility of the central segment to the enzyme's catalytic site. In this review, we consider predictors for cleavage of targeting signals, lipid PTMs, phosphorylation, and glycosylation.
如果翻译后修饰(PTMs)是蛋白质生命周期中由于酶促反应导致的蛋白质一级结构的化学改变,那么酶所识别的底物蛋白质序列中的基序可以作为构建识别数据库序列中PTM位点的预测器的基础。识别基序通常由两个区域组成:第一,一个小的中央片段,它进入酶的催化裂隙,并且对于这种类型的PTM是特异性的;第二,中央部分两侧各有一个约10个或更多具有连接子特征(具有柔性主链的小的极性残基的趋势)的残基的序列环境,这是使中央片段能够接近酶的催化位点所必需的。在本综述中,我们考虑了靶向信号切割、脂质PTM、磷酸化和糖基化的预测器。