The Croonian Lecture 1997. The phosphorylation of proteins on tyrosine: its role in cell growth and disease

Philos Trans R Soc Lond B Biol Sci. 1998 Apr 29;353(1368):583-605. doi: 10.1098/rstb.1998.0228.

Abstract

The reversible phosphorylation of tyrosines in proteins plays a key role in regulating many different processes in eukaryotic organisms, such as growth control, cell cycle control, differentiation cell shape and movement, gene transcription, synaptic transmission, and insulin action. Phosphorylation of proteins is brought about by enzymes called protein-tyrosine kinases that add phosphate to specific tyrosines in target proteins; phosphate is removed from phosphorylated tyrosines by enzymes called protein-tyrosine phosphatases. Phosphorylated tyrosines are recognized by specialized binding domains on other proteins, and such interactions are used to initiate intracellular signaling pathways. Currently, more than 95 protein-tyrosine kinases and more than 55 protein-tyrosine phosphatase genes are known in Homo sapiens. Aberrant tyrosine phosphorylation is a hallmark of many types of cancer and other human diseases. Drugs are being developed that antagonize the responsible protein-tyrosine kinases and phosphatases in order to combat these diseases.

Publication types

  • Historical Article
  • Lecture
  • Review

MeSH terms

  • Animals
  • Cell Division / physiology*
  • Disease / etiology
  • Drug Design
  • Enzyme Inhibitors / pharmacology
  • History, 20th Century
  • Humans
  • Mutation
  • Phosphorylation
  • Protein Tyrosine Phosphatases / chemistry
  • Protein Tyrosine Phosphatases / genetics
  • Protein Tyrosine Phosphatases / metabolism
  • Protein-Tyrosine Kinases / chemistry
  • Protein-Tyrosine Kinases / genetics
  • Protein-Tyrosine Kinases / metabolism
  • Proteins / metabolism*
  • Receptor Protein-Tyrosine Kinases / chemistry
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Research / history
  • Signal Transduction
  • Tyrosine / metabolism*

Substances

  • Enzyme Inhibitors
  • Proteins
  • Tyrosine
  • Protein-Tyrosine Kinases
  • Receptor Protein-Tyrosine Kinases
  • Protein Tyrosine Phosphatases