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Topology Prediction of Helical Transmembrane Proteins: How Far Have We Reached?

机译:螺旋跨膜蛋白的拓扑预测:我们走了多远?

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Transmembrane protein topology prediction methods play important roles in structural biology, because the structure determination of these types of proteins is extremely difficult by the common biophysical, biochemical and molecular biological methods. The need for accurate prediction methods is high, as the number of known membrane protein structures fall far behind the estimated number of these proteins in various genomes. The accuracy of these prediction methods appears to be higher than most prediction methods applied on globular proteins, however it decreases slightly with the increasing number of structures. Unfortunately, most prediction algorithms use common machine learning techniques, and they do not reveal why topologies are predicted with such a high success rate and which biophysical or biochemical properties are important to achieve this level of accuracy. Incorporating topology data determined so far into the prediction methods as constraints helps us to reach even higher prediction accuracy, therefore collection of such topology data is also an important issue.
机译:跨膜蛋白拓扑结构预测方法在结构生物学中起着重要作用,因为通过常见的生物物理,生化和分子生物学方法很难确定这些类型的蛋白的结构。精确的预测方法的需求很高,因为已知的膜蛋白结构的数量远远落后于各种基因组中这些蛋白的估计数量。这些预测方法的准确性似乎比应用于球状蛋白质的大多数预测方法更高,但是随着结构数量的增加,其准确性会略有下降。不幸的是,大多数预测算法使用通用的机器学习技术,并且它们没有揭示为什么以如此高的成功率预测拓扑,以及哪些生物物理或生化特性对于达到此精度水平很重要。将迄今确定的拓扑数据作为约束纳入预测方法有助于我们达到更高的预测精度,因此,收集此类拓扑数据也是一个重要问题。

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