Revealing Unexplored Sequence-Function Space Using Sequence Similarity Networks
Author(s) -
Janine N. Copp,
Eyal Akiva,
Patricia C. Babbitt,
Nobuhiko Tokuriki
Publication year - 2018
Publication title -
biochemistry
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.43
H-Index - 253
eISSN - 1520-4995
pISSN - 0006-2960
DOI - 10.1021/acs.biochem.8b00473
Subject(s) - computational biology , sequence (biology) , function (biology) , similarity (geometry) , protein sequencing , sequence space , biology , protein function , repertoire , sequence alignment , protein structure database , alignment free sequence analysis , peptide sequence , computer science , genetics , sequence database , artificial intelligence , gene , mathematics , physics , acoustics , pure mathematics , banach space , image (mathematics)
The rapidly expanding number of protein sequences found in public databases can improve our understanding of how protein functions evolve. However, our current knowledge of protein function likely represents a small fraction of the diverse repertoire that exists in nature. Integrative computational methods can facilitate the discovery of new protein functions and enzymatic reactions through the observation and investigation of the complex sequence-structure-function relationships within protein superfamilies. Here, we highlight the use of sequence similarity networks (SSNs) to identify previously unexplored sequence and function space. We exemplify this approach using the nitroreductase (NTR) superfamily. We demonstrate that SSN investigations can provide a rapid and effective means to classify groups of proteins, therefore exposing experimentally unexplored sequences that may exhibit novel functionality. Integration of such approaches with systematic experimental characterization will expand our understanding of the functional diversity of enzymes and their associated physiological roles.
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