Biomedical Informatics Center, PGIMER, Chandigarh-160012, India.
BMC Biochem. 2011 May 13;12:20. doi: 10.1186/1471-2091-12-20.
Adenine and guanine phosphates are involved in a number of biological processes such as cell signaling, metabolism and enzymatic cofactor functions. Binding sites in proteins for these ligands are often detected by looking for a previously known motif by alignment based search. This is likely to miss those where a similar binding site has not been previously characterized and when the binding sites do not follow the rule described by predefined motif. Also, it is intriguing how proteins select between adenine and guanine derivative with high specificity.
Residue preferences for AMP, GMP, ADP, GDP, ATP and GTP have been investigated in details with additional comparison with cyclic variants cAMP and cGMP. We also attempt to predict residues interacting with these nucleotides using information derived from local sequence and evolutionary profiles. Results indicate that subtle differences exist between single residue preferences for specific nucleotides and taking neighbor environment and evolutionary context into account, successful models of their binding site prediction can be developed.
In this work, we explore how single amino acid propensities for these nucleotides play a role in the affinity and specificity of this set of nucleotides. This is expected to be helpful in identifying novel binding sites for adenine and guanine phosphates, especially when a known binding motif is not detectable.
腺嘌呤和鸟嘌呤磷酸盐参与许多生物过程,如细胞信号转导、代谢和酶辅助因子功能。通过基于比对的搜索寻找先前已知的模体,可以检测蛋白质中这些配体的结合位点。这种方法可能会错过那些尚未被先前表征的结合位点,以及那些结合位点不符合预定义模体描述的规则的情况。此外,令人好奇的是,蛋白质如何以高特异性在腺嘌呤和鸟嘌呤衍生物之间进行选择。
详细研究了 AMP、GMP、ADP、GDP、ATP 和 GTP 的残基偏好,并与环状变体 cAMP 和 cGMP 进行了额外比较。我们还尝试使用局部序列和进化轮廓信息来预测与这些核苷酸相互作用的残基。结果表明,特定核苷酸的单个残基偏好之间存在细微差异,并且考虑到相邻环境和进化背景,可以开发出它们结合位点预测的成功模型。
在这项工作中,我们探讨了这些核苷酸的单个氨基酸倾向如何在这组核苷酸的亲和力和特异性中发挥作用。这有望有助于识别腺嘌呤和鸟嘌呤磷酸盐的新结合位点,特别是在无法检测到已知结合模体时。