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ProDFace:一种用于剖析蛋白质- DNA界面的网络工具。

ProDFace: A web-tool for the dissection of protein-DNA interfaces.

作者信息

Pal Arumay, Chakrabarti Pinak, Dey Sucharita

机构信息

School of Bioengineering, Vellore Institute of Technology, Bhopal, India.

Department of Biochemistry, Bose Institute, Kolkata, India.

出版信息

Front Mol Biosci. 2022 Sep 6;9:978310. doi: 10.3389/fmolb.2022.978310. eCollection 2022.

Abstract

Protein-DNA interactions play a crucial role in gene expression and regulation. Identifying the DNA binding surface of proteins has long been a challenge-in comparison to protein-protein interactions, limited progress has been made in the development of efficient DNA binding site prediction and proteinDNA docking methods. Here we present ProDFace, a web tool that characterizes the binding region of a protein-DNA complex based on amino acid propensity, hydrogen bond (HB) donor capacity (number of solvent accessible HB donor groups), sequence conservation at the interface core and rim region, and geometry. The program takes as input the structure of a protein-DNA complex in PDB (Protein Data Bank) format, and outputs various physicochemical and geometric parameters of the interface, as well as conservation of the interface residues in the protein component. Values are provided for the whole interface, and after dissecting it into core and rim regions. Details of water mediated HBs between protein and DNA, potential HB donor groups present at the binding surface of protein, and conserved interface residues are also provided as downloadable text files. These parameters can be useful in evaluating and validating protein-DNA docking solutions, structures derived from simulation as well as solutions from the available prediction tools, and facilitate the development of more efficient prediction methods. The web-tool is freely available at structbioinfo.iitj.ac.in/resources/bioinfo/pd_interface

摘要

蛋白质与DNA的相互作用在基因表达和调控中起着至关重要的作用。与蛋白质-蛋白质相互作用相比,识别蛋白质的DNA结合表面长期以来一直是一项挑战,在高效DNA结合位点预测和蛋白质-DNA对接方法的开发方面进展有限。在此,我们展示了ProDFace,这是一种网络工具,可基于氨基酸倾向、氢键(HB)供体能力(溶剂可及HB供体基团的数量)、界面核心和边缘区域的序列保守性以及几何形状来表征蛋白质-DNA复合物的结合区域。该程序以PDB(蛋白质数据库)格式的蛋白质-DNA复合物结构作为输入,并输出界面的各种物理化学和几何参数,以及蛋白质组分中界面残基的保守性。提供了整个界面以及将其分解为核心和边缘区域后的数值。还提供了蛋白质与DNA之间水介导的HB的详细信息、蛋白质结合表面存在的潜在HB供体基团以及保守的界面残基,作为可下载的文本文件。这些参数可用于评估和验证蛋白质-DNA对接解决方案、模拟衍生的结构以及现有预测工具的解决方案,并有助于开发更高效的预测方法。该网络工具可在structbioinfo.iitj.ac.in/resources/bioinfo/pd_interface上免费获取

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76d4/9486321/41dede3094ac/fmolb-09-978310-g001.jpg

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