PROTEIN-PROFEN INTERACTION: THE ROLE OF CARBON IN DEALING ACTIVE SITE INTERACTION

Rajasekaran Ekambaram
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Abstract

Nano force coming from carbon alone was part of our discussions in the earlier calculations. It is found out to be the predominant role of carbon coming from adequacy principle governed from carbon value. Here it is extended to protein-ibuprofen interaction as case study for demonstrating the role played by value of carbon in dealing with internal healing of newly developed situation arising from carbon value. Well all of us sudden take place that the internal carbon demonstrated to be in par with cohesiveness arising out of healing path of drug action. Very well done with interaction and associated movement of atoms in dealing cohesiveness in the protein to accommodate incoming drug of action. Whereas it is noticed that the internal carbon optimized domain (COD) adjusted to be the main part of the dealing with drug delivery to active site rather than van der Waals and electrostatic forces of interaction. Only those that are in accordance are adjusted to new development and all that are rigid are unaltered during intercourse of action. It is noticed that the interaction arising from carbon role will be the main part of interaction that needed to be measured from bond of all atoms involved. In this context, whether or not the measurable quantity may be deviation of the position of individual atoms before and after. We have tested that too and noticed the deviation of internal COD forming elements. That is discussed as part of this new formation of cohesive force and adjustments arising from drug alone are interpreted. With this advancement we might even think of alternative elements to be considered for healing and all. It is going to be the new beginning of alternative treatment for the suffering coming from carbon role and all. force explains all phenomena that are in material which holds strong bond of all forces of attraction: A case study with carbon material.
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蛋白质-洛芬相互作用:碳在处理活性位点相互作用中的作用
来自碳的纳米力是我们在早期计算中讨论的一部分。从碳价值支配的充分性原则中发现了碳的主导作用。这里将其扩展到蛋白质-布洛芬相互作用作为案例研究,以证明碳价值在处理由碳价值引起的新发展情况的内部愈合中所起的作用。我们所有人都突然发现体内的碳与药物作用的愈合过程中产生的凝聚力是一样的。很好地处理了相互作用和相关的原子运动,以处理蛋白质的内聚性,以适应进入的药物作用。然而,注意到内部碳优化结构域(COD)调整为处理药物传递到活性位点的主要部分,而不是相互作用的范德华力和静电力。只有那些符合的才能适应新的发展,而所有死板的东西在行动的交往中是不变的。注意到,碳作用引起的相互作用将是相互作用的主要部分,需要从所有参与的原子的键来测量。在这种情况下,可测量的量是否可能是前后单个原子位置的偏差。我们也进行了测试,注意到内部COD形成元素的偏差。这是作为这种新形成的凝聚力的一部分进行讨论的,并且解释了单独由药物引起的调整。有了这一进步,我们甚至可以考虑治疗等其他因素。这将是替代疗法的新开端,以治疗碳排放带来的痛苦。力解释了所有的现象,在材料中,所有的吸引力的强键:以碳材料为例研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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