The C-terminal Conserved Domain of MARCKS Is Phosphorylated in Vivo by Proline-directed Protein Kinase
Open Access
- 1 February 1998
- journal article
- Published by Elsevier BV
- Vol. 273 (8), 4367-4371
- https://doi.org/10.1074/jbc.273.8.4367
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- GFAP Transgenic MiceMethods, 1996
- Myristoylated Alanine-rich C Kinase Substrate (MARCKS) Produces Reversible Inhibition of Phospholipase C by Sequestering Phosphatidylinositol 4,5-Bisphosphate in Lateral DomainsJournal of Biological Chemistry, 1996
- Site-specific Phosphorylation of Synapsin I by Mitogen-activated Protein Kinase and Cdk5 and Its Effects on Physiological FunctionsJournal of Biological Chemistry, 1996
- [15] Protein structure analysis by mass spectrometryMethods in enzymology, 1996
- MARCKS deficiency in mice leads to abnormal brain development and perinatal death.Proceedings of the National Academy of Sciences of the United States of America, 1995
- The Marcks brothers: A family of protein kinase C substratesCell, 1992
- Relationship between the major protein kinase C substrates acidic 80‐kDa protein‐kinase‐C substrate (80K) and myristoylated alanine‐rich C‐kinase substrate (MARCKS)European Journal of Biochemistry, 1992
- MASS SPECTROMETRY OF PEPTIDES AND PROTEINSAnnual Review of Biochemistry, 1992
- [12] Mass spectrometry of peptides and proteins by matrix-assisted ultraviolet laser desorption/ionizationMethods in enzymology, 1990
- Selective conservation of GAP-43 structure in vertebrate evolutionNeuron, 1989