SynLinker
SynLinker identifies candidate linker peptide sequences for designing recombinant fusion proteins to enable appropriate domain connectivity while preserving structural integrity and functional activity.
Key Features:
- Linker database: A compiled set of 2,260 linker peptide sequences derived from natural linkers extracted from non-redundant multi-domain proteins in the Protein Data Bank (PDB) and artificial/empirical linkers sourced from scientific literature and patents.
- Selection and filtering: Supports selection of linker candidates based on specific selection criteria.
- Fusion assembly and structure prediction: Combines a selected linker with two domain structures appended at the N- and C-terminals and enables prediction of a de novo structure for the resultant fusion protein.
- Multi-domain focus: Targets linker identification for recombinant fusion proteins that connect multiple protein domains to maintain structural integrity and functional activity.
Scientific Applications:
- Synthetic fusion protein design: Identification of optimal linker sequences for engineering recombinant fusion proteins.
- Structural biology: Modeling and prediction of linker effects on domain arrangement and structural stability.
- Biotechnology and (bio)pharmaceutical development: Engineering multi-domain proteins for specific functionalities and therapeutic applications.
Methodology:
Compilation of a database of 2,260 linker sequences from natural linkers extracted from non-redundant multi-domain proteins in the Protein Data Bank (PDB) and artificial/empirical linkers from literature and patents; appended selected linkers between two domain structures at the N- and C-terminals and predicted a de novo structure for the fusion protein.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 8/3/2017
- Last Updated:
- 11/24/2024
Operations
Publications
Liu C, Chin JX, Lee D. SynLinker: an integrated system for designing linkers and synthetic fusion proteins. Bioinformatics. 2015;31(22):3700-3702. doi:10.1093/bioinformatics/btv447. PMID:26227144.