Structural genomics aims to structurally characterize most protein sequences by an efficient combination of experiment and modeling. Central to the success of these efforts is effective target selection. There are a variety of target selection schemes, ranging from focusing on only novel folds to selecting all proteins in a model genome. Many of the target selection strategies of the Structural Genomic Consortiums are biologically based, providing a set of protein targets that are key actors in an interesting biological process. This project aims to provide a flexible tool for general target selection (in this case of Structural Genomics) based on collective knowledge. TDI registered users can vote for genes/proteins that may be promissing candidates for structural determination. The aim of the project is to generate a list of target proteins, which structure may help the advance of drug discovery for malaria. Dr. Raymond Hui, from the Structural Genomics Consortium in Toronto, and Dr Marc A. Marti-Renom, a computational bioligist, from UCSF, will analyze the gene the community voted on to have the highest potential. Results from that analysis will be posted here as well as open-access databases such as PlasmoDB. To contribute to the project you need to login with TSL. We intend to release this project in the early month of 2006.