Literature DB >> 29024246

PixelDB: Protein-peptide complexes annotated with structural conservation of the peptide binding mode.

Vincent Frappier1, Madeleine Duran1, Amy E Keating1,2.   

Abstract

PixelDB, the Peptide Exosite Location Database, compiles 1966 non-redundant, high-resolution structures of protein-peptide complexes filtered to minimize the impact of crystal packing on peptide conformation. The database is organized to facilitate study of structurally conserved versus non-conserved elements of protein-peptide engagement. PixelDB clusters complexes based on the structural similarity of the peptide-binding protein, and by comparing complexes within a cluster highlights examples of domains that engage peptides using more than one binding mode. PixelDB also identifies conserved peptide core structural motifs characteristic of each binding mode. Peptide regions that flank core motifs often make non-structurally conserved interactions with the protein surface in regions we call exosites. Many examples establish that exosite contacts can be important for enhancing protein binding and interaction specificity. PixelDB provides a resource for computational and structural biologists to study, model, and predict core-motif and exosite-contacting peptide interactions. PixelDB is available to the community without restriction in a convenient flat-file format with accompanying visualization tools.
© 2017 The Protein Society.

Keywords:  exosites; peptide binding motifs; peptide docking; protein-peptide interactions; structural biology database

Mesh:

Substances:

Year:  2017        PMID: 29024246      PMCID: PMC5734312          DOI: 10.1002/pro.3320

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


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