期刊文献+

PepBind: A Comprehensive Database and Computational Tool for Analysis of Protein-peptide Interactions 被引量:1

原文传递
导出
摘要 Protein-peptide interactions, where one partner is a globular protein (domain) and the other is a flexible linear peptide, are key components of cellular processes predominantly in signal- ing and regulatory networks, hence are prime targets for drug design. To derive the details of the protein-peptide interaction mechanism is often a cumbersome task, though it can be made easier with the availability of specific databases and tools. The Peptide Binding Protein Database (Pep- Bind) is a curated and searchable repository of the structures, sequences and experimental observa- tions of 3100 protein^eptide complexes. The web interface contains a computational tool, protein inter-chain interaction (PICI), for computing several types of weak or strong interactions at the pro- tein peptide interaction interface and visualizing the identified interactions between residues in Jmol viewer. This initial database release focuses on providing protein-peptide interface informa- tion along with structure and sequence information for protein-peptide complexes deposited in the Protein Data Bank (PDB). Structures in PepBind are classified based on their cellular activity. More than 40% of the structures in the database are found to be involved in different regulatory pathways and nearly 20% in the immune system. These data indicate the importance of protein- peptide complexes in the regulation of cellular processes. PepBind is freely accessible at http:// pepbind.bicpu.edu.in/. Protein-peptide interactions, where one partner is a globular protein (domain) and the other is a flexible linear peptide, are key components of cellular processes predominantly in signal- ing and regulatory networks, hence are prime targets for drug design. To derive the details of the protein-peptide interaction mechanism is often a cumbersome task, though it can be made easier with the availability of specific databases and tools. The Peptide Binding Protein Database (Pep- Bind) is a curated and searchable repository of the structures, sequences and experimental observa- tions of 3100 protein^eptide complexes. The web interface contains a computational tool, protein inter-chain interaction (PICI), for computing several types of weak or strong interactions at the pro- tein peptide interaction interface and visualizing the identified interactions between residues in Jmol viewer. This initial database release focuses on providing protein-peptide interface informa- tion along with structure and sequence information for protein-peptide complexes deposited in the Protein Data Bank (PDB). Structures in PepBind are classified based on their cellular activity. More than 40% of the structures in the database are found to be involved in different regulatory pathways and nearly 20% in the immune system. These data indicate the importance of protein- peptide complexes in the regulation of cellular processes. PepBind is freely accessible at http:// pepbind.bicpu.edu.in/.
出处 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2013年第4期241-246,共6页 基因组蛋白质组与生物信息学报(英文版)
基金 the Department of Biotechnology (Grant No. BT/BI/03/015/2002) Department of Information Technology (Grant No. DIT/R&D/15 (9)2007), Government of India
关键词 Peptide-binding proteinsdatabase PepBind Protein-peptide complex Protein-peptide interface Protein-peptide interactiontool Protein inter-chaininteraction Peptide-binding proteinsdatabase PepBind Protein-peptide complex Protein-peptide interface Protein-peptide interactiontool Protein inter-chaininteraction
  • 相关文献

参考文献48

  • 1Neduva V, Russell RB. Peptides mediating interaction networks: new leads at last. Curr Opin Biotechnol 2006;17:465-71.
  • 2Stanfield RL, Wilson IA. Protein-peptide interactions. Curr Opin Struct Biol 1995;5:103-13.
  • 3Parthasarathi L, Casey F, Stein A, Aloy P, Shields DC. Approved drug mimics of short peptide ligands from protein interaction motifs. J Chem Inf Model 2008;48:1943-8.
  • 4Zhao L, Chmielewski J. Inhibiting protein-protein interactions using designed molecules. Curr Opin Struct Biol 2005;15:31-4.
  • 5Kim JE, Chen J, Lou Z. DBC1 is a negative regulator of SIRT1. Nature 2008;451:583-6.
  • 6Petsalaki E, Russell RB. Peptide-mediated interactions in biolog- ical systems: new discoveries and applications. Curr Opin Biotechnol 2008;19:344-50.
  • 7Vagner J, Qu H, Hruby VJ. Peptidomimetics, a synthetic tool of drug discovery. Curr Opin Chem Biol 2008;12:292-6.
  • 8. Berman HM, Kleywegt G J, Nakamura H, Markley JL. The protein data bank at 40: reflecting on the past to prepare for the future. Structure 2012;20:391-6.
  • 9Dinkel H, Michael S, Weatheritt RJ, Davey NE, Van Roey K, Altenberg B, et al. ELM-the database of eukaryotic linear motifs. Nucleic Acids Res 2012;40:D242-51.
  • 10Dinkel H, Chica C, Via A, Gould CM, Jensen L J, Gibson TJ, et al. Phospho.ELM: a database of phosphorylation sites-update 2011. Nucleic Acids Res 2011;39:D261-7.

同被引文献3

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部