首页> 美国卫生研究院文献>Journal of Ocular Biology Diseases and Informatics >Comparative modeling of retinol-binding protein-3 and retinal S-antigen in Eales’ disease and prediction of their binding sites using computational methods
【2h】

Comparative modeling of retinol-binding protein-3 and retinal S-antigen in Eales’ disease and prediction of their binding sites using computational methods

机译:Eales病中视黄醇结合蛋白3和视网膜S抗原的比较模型和使用计算方法预测其结合位点

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Retinal S-antigen and interphotoreceptor retinoid-binding protein-3 play a significant role in the etiopathogenesis of Eales' disease. Protein 3D structures are functionally very important and play a significant role in progression of the disease, hence these 3D structures are better target for further drug designing and relative studies. We developed 3D model structure of retinol-binding protein-3 and retinal S-antigen protein of human involved in Eales' disease. Functional site prediction is a very important and related step; hence, in the current course of analysis, we predicted putative functional site residues in the target proteins. Molecular models of these proteins of Eales' disease as documented in this study may provide a valuable aid for designing an inhibitor or better ligand against Eales' disease and could play a significant role in drug design.
机译:视网膜S抗原和感光体类维生素A结合蛋白3在Eales病的发病机理中起重要作用。蛋白质3D结构在功能上非常重要,并且在疾病进展中起着重要作用,因此这些3D结构是进一步药物设计和相关研究的更好靶标。我们开发了参与Eales病的人的视黄醇结合蛋白3和视网膜S抗原蛋白的3D模型结构。功能部位预测是非常重要且相关的步骤;因此,在当前的分析过程中,我们预测了目标蛋白中假定的功能位点残基。本研究中记录的这些Eales病蛋白的分子模型可能为设计针对Eales病的抑制剂或更好的配体提供有价值的帮助,并且可能在药物设计中发挥重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号