Gowthaman Ragul, Silvester A Johnwin, Saranya K, Kanya K S Rathna, Archana N R
Department of Bioinformatics, School of Chemical and Biotechnology, Shanmugha Arts Science Technology & Research Academy (SASTRA), SASTRA UNIVERSITY, Tanjore, Tamilnadu, India.
Bioinformation. 2006 Dec 2;1(7):269-75. doi: 10.6026/97320630001269.
Autism is a developmental disability causing learning and memory disorder. The heart of the search for a cure for this syndrome is the need to understand dendrite branch patterning, a process crucial for proper synaptic transmission. Due to the association of snapin with the SNARE complex and its role in synaptic transmission it is reported as a potential drug target for autism therapies. We wish to impart the noesis of the 3D structure of the snapin protein, and in this chase we predict the native structure from its sequence of amino acid residues using the classical Comparative protein structure modeling methods. The predicted protein model can be of great assistance in understanding the structural insights, which is necessary to understand the protein function. Understanding the interactions between snapin and SNARE complex is crucial in studying its role in the neurotransmitter release process. We also presented a computational model that shows the interaction between the snapin and SNAP-25 protein, a part of the larger SNARE complex.
自闭症是一种导致学习和记忆障碍的发育性残疾。寻找该综合征治愈方法的核心在于需要了解树突分支模式,这一过程对正常的突触传递至关重要。由于Snapin与SNARE复合体相关联且在突触传递中发挥作用,它被报道为自闭症治疗的潜在药物靶点。我们希望传递Snapin蛋白三维结构的知识,在此过程中,我们使用经典的比较蛋白质结构建模方法从其氨基酸残基序列预测天然结构。预测的蛋白质模型对理解结构见解有很大帮助,而这对于理解蛋白质功能是必要的。了解Snapin与SNARE复合体之间的相互作用对于研究其在神经递质释放过程中的作用至关重要。我们还提出了一个计算模型,展示了Snapin与SNAP - 25蛋白(更大的SNARE复合体的一部分)之间的相互作用。