Department of Biological Sciences and Bioengineering, Indian Institute of Technology Kanpur, Kanpur, Uttar Pradesh 208016, India.
Mehta Family Centre for Engineering in Medicine, Indian Institute of Technology Kanpur, Kanpur, Uttar Pradesh 208026, India.
Database (Oxford). 2023 Mar 13;2023. doi: 10.1093/database/baad012.
Aquaporins and aquaglyceroporins belong to the superfamily of major intrinsic proteins (MIPs), and they transport water and other neutral solutes such as glycerol. These channel proteins are involved in vital physiological processes and are implicated in several human diseases. Experimentally determined structures of MIPs from diverse organisms reveal a unique hour-glass fold with six transmembrane helices and two half-helices. MIP channels have two constrictions formed by Asn-Pro-Ala (NPA) motifs and aromatic/arginine selectivity filters (Ar/R SFs). Several reports have found associations among single-nucleotide polymorphisms (SNPs) in human aquaporins (AQPs) with diseases in specific populations. In this study, we have compiled 2798 SNPs that give rise to missense mutations in 13 human AQPs. To understand the nature of missense substitutions, we have systematically analyzed the pattern of substitutions. We found several examples in which substitutions could be considered as non-conservative that include small to big or hydrophobic to charged residues. We also analyzed these substitutions in the context of structure. We have identified SNPs that occur in NPA motifs or Ar/R SFs, and they will most certainly disrupt the structure and/or transport properties of human AQPs. We found 22 examples in which missense SNP substitutions that are mostly non-conservative in nature have given rise to pathogenic conditions as found in the Online Mendelian Inheritance in Man database. It is most likely that not all missense SNPs in human AQPs will result in diseases. However, understanding the effect of missense SNPs on the structure and function of human AQPs is important. In this direction, we have developed a database dbAQP-SNP that contains information about all 2798 SNPs. This database has several features and search options that can help the user to find SNPs in specific positions of human AQPs including the functionally and/or structurally important regions. dbAQP-SNP (http://bioinfo.iitk.ac.in/dbAQP-SNP) is freely available to the academic community. Database URL http://bioinfo.iitk.ac.in/dbAQP-SNP.
水通道蛋白和甘油通道蛋白属于主要内在蛋白 (MIP) 超家族,它们运输水和其他中性溶质,如甘油。这些通道蛋白参与重要的生理过程,并与几种人类疾病有关。来自不同生物体的 MIP 的实验确定结构揭示了一种独特的沙漏折叠,具有六个跨膜螺旋和两个半螺旋。MIP 通道有两个由 Asn-Pro-Ala (NPA) 基序和芳香族/精氨酸选择性过滤器 (Ar/R SF) 形成的收缩。有几项报道发现,人类水通道蛋白 (AQP) 中的单核苷酸多态性 (SNP) 与特定人群的疾病之间存在关联。在这项研究中,我们汇编了导致 13 个人类 AQP 产生错义突变的 2798 个 SNP。为了了解错义替换的性质,我们系统地分析了替换模式。我们发现了几个可以被认为是非保守的替换的例子,包括从小到大和从疏水性到带电荷的残基。我们还在结构的背景下分析了这些替换。我们确定了发生在 NPA 基序或 Ar/R SF 中的 SNPs,它们肯定会破坏人类 AQP 的结构和/或运输特性。我们发现了 22 个例子,其中错义 SNP 替换在性质上主要是非保守的,导致了在线孟德尔遗传数据库中发现的致病条件。很可能并非所有人类 AQP 中的错义 SNP 都会导致疾病。然而,了解错义 SNP 对人类 AQP 的结构和功能的影响很重要。在这方面,我们开发了一个包含所有 2798 个 SNP 信息的数据库 dbAQP-SNP。该数据库具有几个功能和搜索选项,可以帮助用户在人类 AQP 的特定位置找到 SNPs,包括功能和/或结构上重要的区域。dbAQP-SNP(http://bioinfo.iitk.ac.in/dbAQP-SNP)可供学术界免费使用。数据库网址 http://bioinfo.iitk.ac.in/dbAQP-SNP。