FEBS Letters 1999-11-19

Kinetic mechanism and ATP-binding site reactivity of p38gamma MAP kinase.

T Fox, M J Fitzgibbon, M A Fleming, H M Hsiao, C L Brummel, M S Su

Index: FEBS Lett. 461(3) , 323-8, (1999)

Full Text: HTML

Abstract

Activated p38gamma MAP kinase exhibited significant basal ATPase activity in the absence of a kinase substrate, and addition of a phosphoacceptor substrate increased k(cat)/K(m)20-fold. AMP-PCP was competitive with ATP binding and non-competitive with phosphoacceptor substrate binding. The nucleotide binding site affinity label 5'-(p-fluorosulfonylbenzoyl)adenosine (FSBA) bound stoichiometrically at Lys-56 in the ATP site of both unphosphorylated and activated p38gamma. AMP-PCP only protected the activated enzyme from FSBA inactivation, implying that AMP-PCP does not bind unphosphorylated p38gamma. Basal ATPase activities were also observed for activated p38alpha, ERK2 and JNK3 suggesting that the enzymatic mechanism may be similar for all classes of MAP kinases.


Related Compounds

  • FSBA

Related Articles:

Radioresistant Sf9 insect cells undergo an atypical form of Bax-dependent apoptosis at very high doses of γ-radiation.

2013-12-01

[Int. J. Radiat. Biol. 89(12) , 1017-27, (2013)]

Wortmannin inactivates phosphoinositide 3-kinase by covalent modification of Lys-802, a residue involved in the phosphate transfer reaction.

1996-04-01

[Mol. Cell. Biol. 16 , 1722-1733, (1996)]

Vesicular transport and apotransferrin in intestinal iron absorption, as shown in the Caco-2 cell model.

2006-02-01

[Am. J. Physiol. Gastrointest. Liver Physiol. 290 , G301-G309, (2006)]

The ATP-binding site of brain phosphatidylinositol 4-kinase PI4K230 as revealed by 5'-p-fluorosulfonylbenzoyladenosine.

2001-03-01

[Int. J. Biochem. Cell Biol. 33(3) , 249-59, (2001)]

5'-p-Fluorosulfonylbenzoyl adenosine inhibits progesterone synthesis in human placental mitochondria.

2002-11-08

[Biochim. Biophys. Acta 1585(1) , 11-8, (2002)]

More Articles...