Akter Nurun Nahar, Uddin Md Moin, Uddin Nesar, Asha Israt Jahan, Uddin Md Soyeb, Hossain Md Arju, Alam Fahadul, Shifat Siratul Kubra, Zihad Md Abu, Rahman Md Habibur
Department of Biotechnology and Genetic Engineering, Noakhali Science and Technology University, Noakhali, Bangladesh.
Department of Biotechnology, Bangladesh Agricultural University, Mymensingh, Bangladesh.
Evol Bioinform Online. 2025 Mar 31;21:11769343251327660. doi: 10.1177/11769343251327660. eCollection 2025.
, a foodborne pathogen with a fatality rate of 33%, is a rod-shaped, Gram-negative, non-spore-forming bacterium responsible for causing meningitis, bacteremia, and necrotizing enterocolitis. Despite many unknown functions of hypothetical proteins in bacterial genomes, bioinformatic techniques have successfully annotated their roles in various pathogens.
The aim of this investigation is to identify and annotate the structural and functional properties of a hypothetical protein (HP) from 7G strain (accession no. WP_004386962.1, 277 residues) using computational tools.
Multiple bioinformatic tools were used to identify the homologous protein and to construct and validate its 3D structure. A 3D model was generated using SWISS-MODEL and validated using tools, developing a reliable 3D structure. The STRING and CASTp servers provided information on protein-protein interactions and active sites, identifying functional partners.
The putative protein was soluble, stable, and localized in the cytoplasmic membranes, indicating its biological activity. Functional annotation identified TagJ (HsiE1) within the protein, a member of the ImpE superfamily involved in the transport of toxins and a part of the bacterial type VI secretion system (T6SS). The 3-dimensional structure of this protein was validated through molecular docking involving 6 different compounds. Among these, ceforanide demonstrated the strongest binding scores, -7.5 kcal/mol for the hypothetical protein and -7.2 kcal/mol for its main template protein (PDB ID: 4UQX.1).
Comparative genomics study suggests that the protein found in may be a viable therapeutic target because it seems distinctive and different from human proteins. The results of multiple sequence alignment (MSA) and molecular docking supported HP's potential involvement as a T6SS. These in silico results represent that the examined HP could be valuable for studying infections and creating medicines to treat -mediated disorders.
[病原体名称]是一种食源性病原体,致死率为33%,是一种杆状、革兰氏阴性、不形成芽孢的细菌,可导致脑膜炎、菌血症和坏死性小肠结肠炎。尽管细菌基因组中的假设蛋白有许多未知功能,但生物信息学技术已成功注释了它们在各种病原体中的作用。
本研究的目的是使用计算工具鉴定和注释来自[病原体名称]7G菌株(登录号WP_004386962.1,277个氨基酸残基)的一种假设蛋白(HP)的结构和功能特性。
使用多种生物信息学工具鉴定同源蛋白,并构建和验证其三维结构。使用SWISS-MODEL生成三维模型,并使用工具进行验证,从而开发出可靠的三维结构。STRING和CASTp服务器提供了蛋白质-蛋白质相互作用和活性位点的信息,确定了功能伙伴。
推测的蛋白是可溶的、稳定的,且定位于细胞质膜中,表明其具有生物活性。功能注释在该蛋白中鉴定出TagJ(HsiE1),它是ImpE超家族的成员,参与毒素运输,是细菌VI型分泌系统(T6SS)的一部分。该蛋白的三维结构通过涉及6种不同化合物的分子对接进行了验证。其中,头孢乙腈显示出最强的结合分数,假设蛋白为-7.5千卡/摩尔,其主要模板蛋白(PDB ID:4UQX.1)为-7.2千卡/摩尔。
比较基因组学研究表明,在[病原体名称]中发现的这种蛋白可能是一个可行的治疗靶点,因为它似乎与人类蛋白不同。多序列比对(MSA)和分子对接的结果支持了HP作为T6SS的潜在作用。这些计算机模拟结果表明,所研究的HP对于研究[病原体名称]感染和开发治疗[病原体名称]介导疾病的药物可能具有重要价值。