John Capra
Last active: 3/3/2020

Predicting functionally important residues from sequence conservation.

Capra JA, Singh M
Bioinformatics. 2007 23 (15): 1875-82

PMID: 17519246 · DOI:10.1093/bioinformatics/btm270

MOTIVATION - All residues in a protein are not equally important. Some are essential for the proper structure and function of the protein, whereas others can be readily replaced. Conservation analysis is one of the most widely used methods for predicting these functionally important residues in protein sequences.

RESULTS - We introduce an information-theoretic approach for estimating sequence conservation based on Jensen-Shannon divergence. We also develop a general heuristic that considers the estimated conservation of sequentially neighboring sites. In large-scale testing, we demonstrate that our combined approach outperforms previous conservation-based measures in identifying functionally important residues; in particular, it is significantly better than the commonly used Shannon entropy measure. We find that considering conservation at sequential neighbors improves the performance of all methods tested. Our analysis also reveals that many existing methods that attempt to incorporate the relationships between amino acids do not lead to better identification of functionally important sites. Finally, we find that while conservation is highly predictive in identifying catalytic sites and residues near bound ligands, it is much less effective in identifying residues in protein-protein interfaces.

AVAILABILITY - Data sets and code for all conservation measures evaluated are available at

MeSH Terms (11)

Algorithms Amino Acids Amino Acid Sequence Conserved Sequence Evolution, Molecular Molecular Sequence Data Proteins Sequence Alignment Sequence Analysis, Protein Sequence Homology, Nucleic Acid Structure-Activity Relationship

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