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Systems-level identification of PKA-dependent signaling in epithelial cells.系统水平鉴定上皮细胞中 PKA 依赖性信号转导。
Proc Natl Acad Sci U S A. 2017 Oct 17;114(42):E8875-E8884. doi: 10.1073/pnas.1709123114. Epub 2017 Oct 2.
2
dbPTM 2016: 10-year anniversary of a resource for post-translational modification of proteins.dbPTM 2016:蛋白质翻译后修饰资源十周年纪念
Nucleic Acids Res. 2016 Jan 4;44(D1):D435-46. doi: 10.1093/nar/gkv1240. Epub 2015 Nov 17.
3
The iceLogo web server and SOAP service for determining protein consensus sequences.用于确定蛋白质共有序列的iceLogo网络服务器和SOAP服务。
Nucleic Acids Res. 2015 Jul 1;43(W1):W543-6. doi: 10.1093/nar/gkv385. Epub 2015 Apr 20.
4
PhosphoSitePlus, 2014: mutations, PTMs and recalibrations.磷酸化位点Plus,2014:突变、翻译后修饰与重新校准。
Nucleic Acids Res. 2015 Jan;43(Database issue):D512-20. doi: 10.1093/nar/gku1267. Epub 2014 Dec 16.
5
Ultradeep human phosphoproteome reveals a distinct regulatory nature of Tyr and Ser/Thr-based signaling.超深度人类磷酸化蛋白质组揭示了基于酪氨酸和丝氨酸/苏氨酸的信号传导的独特调控性质。
Cell Rep. 2014 Sep 11;8(5):1583-94. doi: 10.1016/j.celrep.2014.07.036. Epub 2014 Aug 21.
6
Endogenous carbamylation of renal medullary proteins.肾髓质蛋白的内源性氨甲酰化
PLoS One. 2013 Dec 26;8(12):e82655. doi: 10.1371/journal.pone.0082655. eCollection 2013.
7
Identifying protein kinase target preferences using mass spectrometry.利用质谱技术鉴定蛋白激酶的靶标偏好。
Am J Physiol Cell Physiol. 2012 Oct 1;303(7):C715-27. doi: 10.1152/ajpcell.00166.2012. Epub 2012 Jun 20.
8
Seq2Logo: a method for construction and visualization of amino acid binding motifs and sequence profiles including sequence weighting, pseudo counts and two-sided representation of amino acid enrichment and depletion.Seq2Logo:一种构建和可视化氨基酸结合基序和序列特征的方法,包括序列加权、伪计数以及氨基酸丰度和匮乏的双边表示。
Nucleic Acids Res. 2012 Jul;40(Web Server issue):W281-7. doi: 10.1093/nar/gks469. Epub 2012 May 25.
9
Large-scale phosphoproteomic analysis of membrane proteins in renal proximal and distal tubule.大规模磷酸化蛋白质组学分析肾近端和远端小管中的膜蛋白。
Am J Physiol Cell Physiol. 2011 Apr;300(4):C755-70. doi: 10.1152/ajpcell.00360.2010. Epub 2011 Jan 5.
10
Systematic discovery of in vivo phosphorylation networks.体内磷酸化网络的系统性发现。
Cell. 2007 Jun 29;129(7):1415-26. doi: 10.1016/j.cell.2007.05.052. Epub 2007 Jun 14.

PTM-Logo:一个基于位置特异性背景氨基酸概率生成序列 logo 的程序。

PTM-Logo: a program for generation of sequence logos based on position-specific background amino-acid probabilities.

机构信息

Center of Excellence in Systems Biology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Department of Computer Science, Kasetsart University, Bangkok, Thailand.

出版信息

Bioinformatics. 2019 Dec 15;35(24):5313-5314. doi: 10.1093/bioinformatics/btz568.

DOI:10.1093/bioinformatics/btz568
PMID:31318409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7500089/
Abstract

SUMMARY

Identification of the amino-acid motifs in proteins that are targeted for post-translational modifications (PTMs) is of great importance in understanding regulatory networks. Information about targeted motifs can be derived from mass spectrometry data that identify peptides containing specific PTMs such as phosphorylation, ubiquitylation and acetylation. Comparison of input data against a standardized 'background' set allows identification of over- and under-represented amino acids surrounding the modified site. Conventionally, calculation of targeted motifs assumes a random background distribution of amino acids surrounding the modified position. However, we show that probabilities of amino acids depend on (i) the type of the modification and (ii) their positions relative to the modified site. Thus, software that identifies such over- and under-represented amino acids should make appropriate adjustments for these effects. Here we present a new program, PTM-Logo, that generates representations of these amino acid preferences ('logos') based on position-specific amino-acid probability backgrounds calculated either from user-input data or curated databases.

AVAILABILITY AND IMPLEMENTATION

PTM-Logo is freely available online at http://sysbio.chula.ac.th/PTMLogo/ or https://hpcwebapps.cit.nih.gov/PTMLogo/.

SUPPLEMENTARY INFORMATION

Supplementary data are available at Bioinformatics online.

摘要

摘要

鉴定蛋白质中受翻译后修饰(PTM)靶向的氨基酸基序对于理解调控网络非常重要。关于靶向基序的信息可以从鉴定含有特定 PTM(如磷酸化、泛素化和乙酰化)的肽的质谱数据中获得。将输入数据与标准化的“背景”集进行比较,可以鉴定修饰位点周围过度和不足的氨基酸。传统上,靶向基序的计算假设修饰位置周围的氨基酸具有随机背景分布。然而,我们表明,氨基酸的概率取决于(i)修饰的类型和(ii)它们相对于修饰位点的位置。因此,识别这些过度和不足的氨基酸的软件应该对这些影响进行适当的调整。在这里,我们提出了一个新的程序,PTM-Logo,它根据从用户输入数据或经过整理的数据库计算的位置特异性氨基酸概率背景,生成这些氨基酸偏好的表示(“标志”)。

可用性和实现

PTM-Logo 可在 http://sysbio.chula.ac.th/PTMLogo/ 或 https://hpcwebapps.cit.nih.gov/PTMLogo/ 在线免费获得。

补充信息

补充数据可在 Bioinformatics 在线获得。