ADAPTABLE: a comprehensive web platform of antimicrobial peptides tailored to the user's research

被引:32
作者
Ramos-Martin, Francisco [1 ]
Annaval, Thibault [1 ]
Buchoux, Sebastien [1 ]
Sarazin, Catherine [1 ]
D'Amelio, Nicola [1 ]
机构
[1] Univ Picardie Jules Verne, CNRS, Unite Mixte Rech 7025, Genie Enzymat & Cellulaire, Amiens, France
关键词
PROTEIN-STRUCTURE; I-TASSER; DATABASE; PREDICTION; SEQUENCES; CONOSERVER; DIVERSITY; DESIGN; TOOL;
D O I
10.26508/lsa.201900512
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antimicrobial peptides (AMPs) are part of the innate immune response to pathogens in all of the kingdoms of life. They have received significant attention because of their extraordinary variety of activities, in particular, as candidate drugs against the threat of super-bacteria. A systematic study of the relation between the sequence and the mechanism of action is urgently needed, given the thousands of sequences already in multiple web resources. ADAPTABLE web platform (http://gec.u-picardie.fr/adaptable) introduces the concept of "property alignment" to create families of property and sequence-related peptides (SR families). This feature provides the researcher with a tool to select those AMPs meaningful to their research from among more than 40,000 nonredundant sequences. Selectable properties include the target organism and experimental activity concentration, allowing selection of peptides with multiple simultaneous actions. This is made possible by ADAPTABLE because it not only merges sequences of AMP databases but also merges their data, thereby standardizing values and handling non-proteinogenic amino acids. In this unified platform, SR families allow the creation of peptide scaffolds based on common traits in peptides with similar activity, independently of their source.
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页数:11
相关论文
共 89 条
[1]   CPPsite 2.0: a repository of experimentally validated cell-penetrating peptides [J].
Agrawal, Piyush ;
Bhalla, Sherry ;
Usmani, Salman Sadullah ;
Singh, Sandeep ;
Chaudhary, Kumardeep ;
Raghava, Gajendra P. S. ;
Gautam, Ankur .
NUCLEIC ACIDS RESEARCH, 2016, 44 (D1) :D1098-D1103
[2]   Overlap and diversity in antimicrobial peptide databases: compiling a non-redundant set of sequences [J].
Aguilera-Mendoza, Longendri ;
Marrero-Ponce, Yovani ;
Tellez-Ibarra, Roberto ;
Llorente-Quesada, Monica T. ;
Salgado, Jesus ;
Barigye, Stephen J. ;
Liu, Jun .
BIOINFORMATICS, 2015, 31 (15) :2553-2559
[3]   The Mechanisms of Action of Cationic Antimicrobial Peptides Refined by Novel Concepts from Biophysical Investigations [J].
Aisenbrey, Christopher ;
Marquette, Arnaud ;
Bechinger, Burkhard .
ANTIMICROBIAL PEPTIDES: BASICS FOR CLINICAL APPLICATION, 2019, 1117 :33-64
[4]   Peptide consensus sequence determination for the enhancement of the antimicrobial activity and selectivity of antimicrobial peptides [J].
Almaaytah, Ammar ;
Ajingi, Ya'u ;
Abualhaijaa, Ahmad ;
Tarazi, Shadi ;
Alshar'i, Nizar ;
Al-Balas, Qosay .
INFECTION AND DRUG RESISTANCE, 2017, 10 :1-17
[5]  
[Anonymous], 2015, DEV COMP IMMUNOL, DOI DOI 10.1016/j.dci.2014.05.020
[6]  
[Anonymous], HOST DEFENSE PEPTIDE
[7]  
[Anonymous], 2015, BASH 4 3 REFERENCE M
[8]  
[Anonymous], GAWK EFFECTIVE AWK P
[9]  
[Anonymous], 2019, NUCLEIC ACIDS RES, DOI DOI 10.1093/nar/gky1033
[10]  
[Anonymous], SCIENCE