دورية أكاديمية

In silico assessment of the possible pathogenetic effect of the missense variant c.441G>A p.(Met147Ile) of the SLC26A4 gene on the function/structure of the pendrin protein using the AlfhаFold neural network algorithm ; In silico оценка возможного патогенетического влияния миссенс варианта c.441G>A p.(Met147Ile) гена SLC26A4 на функцию/структуру белка пендрина с применением нейросетевого алгоритма AlfhаFold

التفاصيل البيبلوغرافية
العنوان: In silico assessment of the possible pathogenetic effect of the missense variant c.441G>A p.(Met147Ile) of the SLC26A4 gene on the function/structure of the pendrin protein using the AlfhаFold neural network algorithm ; In silico оценка возможного патогенетического влияния миссенс варианта c.441G>A p.(Met147Ile) гена SLC26A4 на функцию/структуру белка пендрина с применением нейросетевого алгоритма AlfhаFold
المؤلفون: V. G. Pshennikova, G. P. Romanov, L. A. Klarov, N. A. Barashkov, В. Г. Пшенникова, Г. П. Романов, Л. А. Кларов, Н. А. Барашков
المصدر: Medical Genetics; Том 21, № 6 (2022); 37-48 ; Медицинская генетика; Том 21, № 6 (2022); 37-48 ; 2073-7998
بيانات النشر: Publishing House «Genius Media» LLC
سنة النشر: 2022
المجموعة: Medical Genetics (E-Journal) / Медицинская генетика
مصطلحات موضوعية: Якутия, missense variant, SLC26A4 gene, pendrin protein (SLC26A4), AlfhaFold system, Yakutia, миссенс-замена, ген SLC26A4, белок пендрин (SLC26A4), система AlfhаFold
الوصف: In this work, for the first time, an in silico evaluation of the possible pathogenic effect of the c.441G>A p.(Met147Ile) variant of uncertain significance of the SLC26A4 gene on the function/structure of the pendrin (SLC26A4) protein was performed using the AlphaFold neural network algorithm, which predicts the spatial structure of the protein when such a structure is unknown. Based on the predicted model of the human pendrin tertiary structure, the alignment of the mutant (p.Met147Ile) and native protein structures was carried out using the PyMOL graphics program. As a result, the calculated similarity index of the two structures RMSD (root-mean-square deviation of atomic positions) was less than 2 Å, which indicates that the missense p.(Met147Ile) substitution theoretically does not violate the structural stability of the protein. Probably, the pathogenic effect of the mutation occurs at the functional level, since the analyzed p.(Met147Ile) is located in a critical region of the core domain (an evolutionarily conserved α3-helix region of the TMD), the disruption of which can lead to incorrect substrate transport or the appearance of toxic conformations in the transmembrane region. ; В работе впервые проведена in silico оценка возможного патогенетического влияния варианта c.441G>A p.(Met147Ile) гена SLC26A4, имеющего в настоящее время статус -вариант неопределенного значения (US - uncertain significance), на функцию/структуру белка пендрина (SLC26A4), выполненного при помощи нейросетевого алгоритма AlphaFold, предсказывающего пространственную структуру белка, когда подобная структура неизвестна. На основе предсказанной модели третичной структуры пендрина человека, было проведено выравнивание мутантной (p.Met147Ile) и нативной структуры белка с помощью графической программы PyMOL. В результате рассчитанный показатель сходства двух структур RMSD (среднеквадратичное отклонение положения атомов) составил меньше 2 Å, то есть миссенс замена p.(Met147Ile) теоретически не нарушает структурную стабильность ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: Russian
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DOI: 10.25557/2073-7998.2022.06.37-48
الإتاحة: https://doi.org/10.25557/2073-7998.2022.06.37-48Test
https://doi.org/10.1152/ajpcell.2000.278.1.C207Test
https://doi.org/10.1210/endo.141.2.7303Test
https://doi.org/10.1097/00041552-200109000-00020Test
https://doi.org/10.1159/000335103Test
https://doi.org/10.1681/ASN.2012080787Test
https://doi.org/10.1073/pnas.82.18.6362Test
https://doi.org/10.1371/journal.pone.0014041Test
https://doi.org/10.25557/2073-7998.2021.09.14-25Test
https://doi.org/10.1016/j.ijporl.2010.06.002Test
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رقم الانضمام: edsbas.AC431B00
قاعدة البيانات: BASE