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使用PEPTIDEMASS进行详细的肽段表征——一个可通过万维网访问的工具。

Detailed peptide characterization using PEPTIDEMASS--a World-Wide-Web-accessible tool.

作者信息

Wilkins M R, Lindskog I, Gasteiger E, Bairoch A, Sanchez J C, Hochstrasser D F, Appel R D

机构信息

Central Clinical Chemistry Laboratory, Geneva University Hospital, Switzerland.

出版信息

Electrophoresis. 1997 Mar-Apr;18(3-4):403-8. doi: 10.1002/elps.1150180314.

Abstract

In peptide mass fingerprinting, there are frequently peptides whose masses cannot be explained. These are usually attributed to either a missed cleavage site during the chemical or enzymatic cutting process, the lack of reduction and alkylation of a protein, protein modifications like the oxidation of methionine, or the presence of protein post-translational modifications. However, they could equally be due to database errors, unusual splicing events, variants of a protein in a population, or artifactual protein modifications. Unfortunately the verification of each of these possibilities can be tedious and time-consuming. To better utilize annotated protein databases for the understanding of peptide mass fingerprinting data, we have written the program "PEPTIDEMASS". This program generates the theoretical peptide masses of any protein in the SWISS-PROT database, or of any sequence specified by the user. If the sequence is derived from the SWISS-PROT database, the program takes into account any annotations for that protein in order to generate the peptide masses. In this manner, the user can obtain the predicted masses of peptides from proteins which are known to have signal sequences, propeptides, transit peptides, simple post-translational modifications, and disulfide bonds. Users are also warned if any peptide masses are subject to change from protein isoforms, database conflicts, or an mRNA splicing variation. The program is freely accessible to the scientific community via the ExPASy World Wide Web server, at the URL address: http://www.expasy.ch/www/tools.html.

摘要

在肽质量指纹图谱中,经常会出现一些肽段,其质量无法得到解释。这些通常归因于化学或酶切过程中遗漏的切割位点、蛋白质还原和烷基化的缺失、蛋白质修饰(如甲硫氨酸氧化)或蛋白质翻译后修饰的存在。然而,它们同样可能是由于数据库错误、异常剪接事件、群体中蛋白质的变体或人为的蛋白质修饰。不幸的是,对这些可能性逐一进行验证可能既繁琐又耗时。为了更好地利用注释的蛋白质数据库来理解肽质量指纹图谱数据,我们编写了“PEPTIDEMASS”程序。该程序可生成SWISS-PROT数据库中任何蛋白质或用户指定的任何序列的理论肽质量。如果序列来自SWISS-PROT数据库,程序会考虑该蛋白质的任何注释以生成肽质量。通过这种方式,用户可以从已知具有信号序列、前肽、转运肽、简单翻译后修饰和二硫键的蛋白质中获得预测的肽质量。如果任何肽质量因蛋白质异构体、数据库冲突或mRNA剪接变异而可能发生变化,程序也会向用户发出警告。科学界可通过ExPASy万维网服务器免费访问该程序,网址为:http://www.expasy.ch/www/tools.html。

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