首页> 外文期刊>Current pharmaceutical design >In silico approaches towards the understanding of the structure-function relationships in metabotropic glutamate receptors (mGluRs) and other family C GPRCs.
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In silico approaches towards the understanding of the structure-function relationships in metabotropic glutamate receptors (mGluRs) and other family C GPRCs.

机译:在计算机上理解代谢型谷氨酸受体(mGluRs)和其他家族C GPRCs中的结构-功能关系的方法。

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摘要

Family C of the superfamily of G-protein coupled receptors is a growing family of heptahelical receptors, which includes, among others, metabotropic glutamate receptors (mGluRs) and GABA(B) receptors. A common feature of all the members of family C is a structural architecture much more complex than any other GPCRs. Computational studies, including homology modeling, pharmacophore definitions and molecular dynamics simulations have constantly flanked experimental approaches in the understanding of the receptor functioning. The present review will discuss the evolution of our perception in family C GPCRs structure and function as emerged from the critical comparison of in silico methods with molecular biology and crystallographic experiments.
机译:G蛋白偶联受体超家族的C族是越来越多的七螺旋受体家族,其中包括代谢型谷氨酸受体(mGluRs)和GABA(B)受体。 C族所有成员的共同特征是结构体系比任何其他GPCR都要复杂得多。计算研究,包括同源性建模,药效团定义和分子动力学模拟,在理解受体功能方面一直处于实验方法的旁边。本综述将讨论我们对家族C GPCR结构和功能的认识演变,这是通过计算机方法与分子生物学和晶体学实验的严格比较得出的。

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