4.4 Article

Discovery of protein-palmitoylating enzymes

期刊

PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
卷 456, 期 6, 页码 1199-1206

出版社

SPRINGER
DOI: 10.1007/s00424-008-0465-x

关键词

protein palmitoylation; DHHC protein; lipid modification; protein targeting; palmitoyl-acyl transferase

资金

  1. Japan Society for the Promotion of Science
  2. Human Frontier Science Program (HFSP)
  3. Ministry of Education, Culture, Sports, Science and Technology (MEXT) [18700376]
  4. HFSP, MEXT [18022054, 18057032, 18687008]
  5. Ministry of Health, Labour and Welfare of Japan [17C-2]

向作者/读者索取更多资源

Posttranslational modification provides proteins with additional function and regulatory control beyond genomic information, allowing cells to maintain homeostasis and respond to extracellular signals. Protein palmitoylation, the common posttranslational modification with the lipid palmitate, plays a pivotal role in protein trafficking and function. Palmitoylation is unique in that it is reversible and dynamically regulated by specific extracellular signals. The reversible nature of protein palmitoylation enables proteins to shuttle between intracellular compartments upon extracellular signals. However, the molecular mechanisms of protein palmitoylation have long been elusive, mostly because the enzymes responsible for protein palmitoylation were unknown. Recently, genetically conserved DHHC family proteins have emerged as palmitoyl-acyl transferases. With the identification of specific enzymes for palmitoylated proteins, including H-Ras, PSD-95, and eNOS, the specificity and regulatory mechanism of DHHC enzymes are beginning to be clarified.

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