Beitz Eric
Dept. of Pharmaceutical Chemistry, University of Tübingen, Morgenstelle 8, 72076 Tübingen, Germany.
BMC Bioinformatics. 2006 Jun 21;7:313. doi: 10.1186/1471-2105-7-313.
Recognition of relevant sequence deviations can be valuable for elucidating functional differences between protein subfamilies. Interesting residues at highly conserved positions can then be mutated and experimentally analyzed. However, identification of such sites is tedious because automated approaches are scarce.
Subfamily logos visualize subfamily-specific sequence deviations. The display is similar to classical sequence logos but extends into the negative range. Positive, upright characters correspond to residues which are characteristic for the subfamily, negative, upside-down characters to residues typical for the remaining sequences. The symbol height is adjusted to the information content of the alignment position. Residues which are conserved throughout do not appear.
Subfamily logos provide an intuitive display of relevant sequence deviations. The method has proven to be valid using a set of 135 aligned aquaporin sequences in which established subfamily-specific positions were readily identified by the algorithm.
识别相关的序列偏差对于阐明蛋白质亚家族之间的功能差异可能很有价值。然后可以对高度保守位置上有趣的残基进行突变并进行实验分析。然而,由于自动化方法稀缺,识别这些位点很繁琐。
亚家族标识可视化亚家族特异性序列偏差。其显示类似于经典序列标识,但延伸到负值范围。正向、直立的字符对应于该亚家族特有的残基,负向、倒置的字符对应于其余序列典型的残基。符号高度根据比对位置的信息含量进行调整。完全保守的残基不会出现。
亚家族标识直观地展示了相关的序列偏差。使用一组135个比对的水通道蛋白序列进行验证,该算法能够轻松识别已确定的亚家族特异性位置,证明了该方法的有效性。