Determinants for substrate phosphorylation by p21-activated protein kinase (γ-PAK)

Polygena T. Tuazon, William C. Spanos, Edwin L. Gump, Curtis A. Monnig, Jolinda A. Traugh

Research output: Contribution to journalArticlepeer-review

60 Scopus citations

Abstract

γ-PAK, originally designated PAK I and subsequently identified as a member of the p21-activated protein kinase family, has been shown to have cytostatic properties and to be involved in maintaining cells in a nondividing state [Rooney, R. D., et al., (1996) J. Biol. Chem. 271, 21498- 21504]. The determinants for phosphorylation of substrates by γ-PAK have been identified by examining the kinetics of phosphorylation of a series of synthetic peptides patterned after the sequence KKRKSGL, which is the site phosphorylated by γ-PAK in the Rous sarcoma virus nucleocapsid protein NC in vivo and in vitro. With these peptides, the recognition sequence for γ-PAK has been shown to contain two basic amino acids in the -2 and -3 positions, as represented by (K/R)RXS, in which the -2 position is an arginine the -3 position is an arginine or a lysine, and X can be an acidic, basic, or neutral amino acid. A basic amino acid in the -1 or -4 position improves the rate of phosphorylation by increasing the V(max) and decreasing the K(m). An acidic amino acid in the -1 position increases the rate (2.5-fold), as does an acidic residue in the -4 position, although to a lower extent (1.6-fold). Proline in the -1 or +1 position has a deleterious effect and inhibits phosphorylation by γ-PAK. The substrate requirements of protein kinases that recognize basic amino acids on the N-terminal side of the phosphorylatable residue such as cAMp-dependent protein kinase (PKA) and Ca2+/phospholipid- dependent protein kinase (PKC) have been compared with γ-PAK using the same peptides. An acidic residue in the -1 position negatively affects PKA and PKC; thus, peptides containing the sequence KRES can be used to identify γ- PAK.

Original languageEnglish (US)
Pages (from-to)16059-16064
Number of pages6
JournalBiochemistry
Volume36
Issue number51
DOIs
StatePublished - 1997
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry

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