Space-related pharma-motifs for fast search of protein binding motifs and polypharmacological targets
Autor: | Li Zen Chang, Kai Cheng Hsu, Jinn-Moon Yang, Chih Ta Lin, Chun-Yu Lin, Yi Yuan Chiu |
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Rok vydání: | 2012 |
Předmět: |
Isoleucine-tRNA Ligase
Protein structure database lcsh:QH426-470 lcsh:Biotechnology Amino Acid Motifs Plasma protein binding Biology Proteomics Piperazines User-Computer Interface Protein structure Protein sequencing Exponential growth lcsh:TP248.13-248.65 Genetics Databases Protein Internet Drug discovery Proteins Protein Structure Tertiary Proto-Oncogene Proteins c-kit lcsh:Genetics Mupirocin Pyrimidines Proceedings Benzamides Imatinib Mesylate DNA microarray Software Protein Binding Biotechnology |
Zdroj: | BMC Genomics, Vol 13, Iss Suppl 7, p S21 (2012) BMC Genomics |
ISSN: | 1471-2164 |
Popis: | Background To discover a compound inhibiting multiple proteins (i.e. polypharmacological targets) is a new paradigm for the complex diseases (e.g. cancers and diabetes). In general, the polypharmacological proteins often share similar local binding environments and motifs. As the exponential growth of the number of protein structures, to find the similar structural binding motifs (pharma-motifs) is an emergency task for drug discovery (e.g. side effects and new uses for old drugs) and protein functions. Results We have developed a Space-Related Pharmamotifs (called SRPmotif) method to recognize the binding motifs by searching against protein structure database. SRPmotif is able to recognize conserved binding environments containing spatially discontinuous pharma-motifs which are often short conserved peptides with specific physico-chemical properties for protein functions. Among 356 pharma-motifs, 56.5% interacting residues are highly conserved. Experimental results indicate that 81.1% and 92.7% polypharmacological targets of each protein-ligand complex are annotated with same biological process (BP) and molecular function (MF) terms, respectively, based on Gene Ontology (GO). Our experimental results show that the identified pharma-motifs often consist of key residues in functional (active) sites and play the key roles for protein functions. The SRPmotif is available at http://gemdock.life.nctu.edu.tw/SRP/. Conclusions SRPmotif is able to identify similar pharma-interfaces and pharma-motifs sharing similar binding environments for polypharmacological targets by rapidly searching against the protein structure database. Pharma-motifs describe the conservations of binding environments for drug discovery and protein functions. Additionally, these pharma-motifs provide the clues for discovering new sequence-based motifs to predict protein functions from protein sequence databases. We believe that SRPmotif is useful for elucidating protein functions and drug discovery. |
Databáze: | OpenAIRE |
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