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Mxi2, a mitogen-activated protein kinase that recognizes and phosphorylates Max protein.

ABSTRACT: We describe Mxi2, a human protein that interacts with Max protein, the heterodimeric partner of the Myc oncoprotein. Mxi2 encodes a 297-residue protein whose sequence indicates that it is related to extracellular signal-regulated kinases (ERK protein kinases). Mxi2 in yeast interacts with Max and with the C terminus of c-Myc. Mxi2 phosphorylates Max both in vitro and in vivo. The Mxi2 putative substrate recognition region has sequence similarity to the helix-loop-helix region in Max and c-Myc, suggesting that substrate recognition might be mediated via this motif. Phosphorylation by Mxi2 may affect the ability of Max to oligomerize with itself and its partners, bind DNA, or regulate gene expression.

SUBMITTER: Zervos AS

PROVIDER: S-EPMC40645 | biostudies-other | 1995 Nov

REPOSITORIES: biostudies-other

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Mxi2, a mitogen-activated protein kinase that recognizes and phosphorylates Max protein.

Zervos A S AS Faccio L L Gatto J P JP Kyriakis J M JM Brent R R

Proceedings of the National Academy of Sciences of the United States of America 19951101 23

We describe Mxi2, a human protein that interacts with Max protein, the heterodimeric partner of the Myc oncoprotein. Mxi2 encodes a 297-residue protein whose sequence indicates that it is related to extracellular signal-regulated kinases (ERK protein kinases). Mxi2 in yeast interacts with Max and with the C terminus of c-Myc. Mxi2 phosphorylates Max both in vitro and in vivo. The Mxi2 putative substrate recognition region has sequence similarity to the helix-loop-helix region in Max and c-Myc, s ...[more]

PMID: 7479834

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