iCTX-type: a sequence-based predictor for identifying the types of conotoxins in targeting ion channels.

Conotoxins are small disulfide-rich neurotoxic peptides, which can bind to ion channels with very high specificity and modulate their activities. Over the last few decades, conotoxins have been the drug candidates for treating chronic pain, epilepsy, spasticity, and cardiovascular diseases. According to their functions and targets, conotoxins are generally categorized into three types: potassium-channel type, sodium-channel type, and calcium-channel types.

Using over-represented tetrapeptides to predict protein submitochondria locations.

The mitochondrion is a key organelle of eukaryotic cell that provides the energy for cellular activities. Correctly identifying submitochondria locations of proteins can provide plentiful information for understanding their functions. However, using web-experimental methods to recognize submitochondria locations of proteins are time-consuming and costly.

Prediction of the types of ion channel-targeted conotoxins based on radial basis function network.

Conotoxins are small disulfide-rich peptide toxins, which have the exceptional diversity of sequences. Because conotoxins are able to specifically bind to ion channels and interfere with neurotransmission, they are considered as the excellent pharmacological candidates in drug design. Appropriate type assignment of newly sequenced mature ion channel-targeted conotoxins with computational method is conducive to explore the biological and pharmacological functions of conotoxins.

Identification of mycobacterial membrane proteins and their types using over-represented tripeptide compositions.

Mycobacterium can cause many serious diseases, such as tuberculosis and leprosy. Its membrane proteins play a critical role for multidrug-resistance and its tenacious survival ability. Knowing the types of membrane proteins will provide novel insights into understanding their functions and facilitate drug target discovery.