PeptiSite: A structural database of peptide binding sites in 4D

被引:10
作者
Acharya, Chayan [1 ]
Kufareva, Irina [1 ]
Ilatovskiy, Andrey V. [1 ,2 ,3 ,4 ]
Abagyan, Ruben [1 ]
机构
[1] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[2] Petersburg Nucl Phys Inst, Div Mol & Radiat Biophys, Gatchina 188300, Russia
[3] PNPI, Res & Educ Ctr Biophys, St Petersburg 195251, Russia
[4] St Petersburg State Polytech Univ, St Petersburg 195251, Russia
关键词
PeptiSite; Peptide binding site; Pocketome; Induced-fit; SiteFinder; MULTIPLE RECEPTOR CONFORMATIONS; DEPENDENT ROTAMER LIBRARY; SIDE-CHAIN FLEXIBILITY; DE-NOVO DESIGN; PROTEIN FLEXIBILITY; MOLECULAR DOCKING; INDUCED FIT; LIGAND-BINDING; DRUG DESIGN; PARTIAL AGONISTS;
D O I
10.1016/j.bbrc.2013.12.132
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We developed PeptiSite, a comprehensive and reliable database of biologically and structurally characterized peptide-binding sites, in which each site is represented by an ensemble of its complexes with protein, peptide and small molecule partners. The unique features of the database include: (1) the ensemble site representation that provides a fourth dimension to the otherwise three dimensional data, (2) comprehensive characterization of the binding site architecture that may consist of a multimeric protein assembly with cofactors and metal ions and (3) analysis of consensus interaction motifs within the ensembles and identification of conserved determinants of these interactions. Currently the database contains 585 proteins with 650 peptide-binding sites. http://peptisite.ucsd.edu/ link allows searching for the sites of interest and interactive visualization of the ensembles using the ActiveICM web-browser plugin. This structural database for protein-peptide interactions enables understanding of structural principles of these interactions and may assist the development of an efficient peptide docking benchmark. (c) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:717 / 723
页数:7
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