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Updated: Aug 8, 2026

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
Published on: May 22, 2018
A genomic perspective on human proteases as drug targets
1Head of Computational Biology, Gemini Genomics (UK), 162 Science Park, Milton Road, CB4 0GH, tel.: +44 (0) 1223-435342; fax: +44 (0) 1223-435301, Cambridge, UK
Abstract:
Of the approximately 400 known human proteases, approximately 14% are under investigation as drug targets. Although the total is certain to rise during the finishing phase of the human genome project, the initial annotation of the approximately 30,000 human proteome set includes approximately 500 proteases. Bioinformatic analysis can now be performed on complete human protease families and will soon include comparisons with mice and fish. New sequences will require evaluation of their function in normal physiology and human disease. By revealing details such as splice variants and population polymorphisms, genomic sequence information will have a central role in the validation of protease drug targets.
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