RT Journal Article
SR Electronic
T1 HMMER Cut-off Threshold Tool (HMMERCTTER): Supervised Classification of Superfamily Protein Sequences with a reliable Cut-off Threshold
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 130443
DO 10.1101/130443
A1 Inti Anabela Pagnuco
A1 María Victoria Revuelta
A1 Hernán Gabriel Bondino
A1 Marcel Brun
A1 Arjen ten Have
YR 2017
UL http://biorxiv.org/content/early/2017/04/24/130443.abstract
AB Protein superfamilies can be divided into subfamilies of proteins with different functional characteristics. Their sequences can be classified hierarchically, which is part of sequence function assignation. Typically, there are no clear subfamily hallmarks that would allow pattern-based function assignation by which this task is mostly achieved based on the similarity principle. This is hampered by the lack of a score cut-off that is both sensitive and specific.HMMER Cut-off Threshold Tool (HMMERCTTER) adds a reliable cut-off threshold to the popular HMMER. Using a high quality superfamily phylogeny, it clusters a set of training sequences such that the cluster-specific HMMER profiles show 100% precision and recall (P&R), thereby generating a specific threshold as inclusion cut-off. Profiles and threshold are then used as classifiers to screen a target dataset. Iterative inclusion of novel sequences to clusters and the corresponding HMMER profiles results in high sensitivity while specificity is maintained by imposing 100% P&R. In three presented case studies of protein superfamilies, classification of large datasets with 100% P&R was achieved with over 95% coverage. Limits and caveats are presented and explained.HMMERCTTER is a promising protein superfamily sequence classifier provided high quality training datasets are used. It provides a decision support system that aids in the difficult task of sequence function assignation in the twilight zone of sequence similarity.Author summary The enormous amount of genome sequences made available in the last decade provide new challenges for scientists. An important step in genome sequence processing is function assignation of the encoded protein sequences, typically based on the similarity principle: The more similar sequences are, the more likely they encode the same function. However, evolution generated many protein superfamilies that consist of various subfamilies with different functional characteristics, such as substrate specificity, optimal activity conditions or the catalyzed reaction. The classification of superfamily sequences to their respective subfamilies can be performed based on similarity but since the different subfamilies also remain similar, it requires a reliable similarity score cut-off.We present a tool that clusters training sequences and describes them in profiles that identify cluster members with higher similarity scores than non-cluster members, i.e. with 100% precision and recall. This defines a score cut-off threshold. Profiles and thresholds are then used to classify other sequences. Classified sequences are included in the profiles in order to improve sensitivity while maintaining specificity by imposing 100% precision and recall. Results on three case studies show that the tool can correctly classify complex superfamilies with over 95% coverage.