Niphakis_2014_Annu.Rev.Biochem_83_341

Reference

Title : Enzyme inhibitor discovery by activity-based protein profiling - Niphakis_2014_Annu.Rev.Biochem_83_341
Author(s) : Niphakis MJ , Cravatt BF
Ref : Annual Review of Biochemistry , 83 :341 , 2014
Abstract :

Eukaryotic and prokaryotic organisms possess huge numbers of uncharacterized enzymes. Selective inhibitors offer powerful probes for assigning functions to enzymes in native biological systems. Here, we discuss how the chemical proteomic platform activity-based protein profiling (ABPP) can be implemented to discover selective and in vivo-active inhibitors for enzymes. We further describe how these inhibitors have been used to delineate the biochemical and cellular functions of enzymes, leading to the discovery of metabolic and signaling pathways that make important contributions to human physiology and disease. These studies demonstrate the value of selective chemical probes as drivers of biological inquiry.

PubMedSearch : Niphakis_2014_Annu.Rev.Biochem_83_341
PubMedID: 24905785

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Citations formats

Niphakis MJ, Cravatt BF (2014)
Enzyme inhibitor discovery by activity-based protein profiling
Annual Review of Biochemistry 83 :341

Niphakis MJ, Cravatt BF (2014)
Annual Review of Biochemistry 83 :341