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

التفاصيل البيبلوغرافية
العنوان: Mxi2, a mitogen-activated protein kinase that recognizes and phosphorylates Max protein
المؤلفون: Lucia Faccio, Roger Brent, Antonis S. Zervos, John M. Kyriakis, Joseph P. Gatto
المصدر: Proceedings of the National Academy of Sciences of the United States of America. 92(23)
سنة النشر: 1995
مصطلحات موضوعية: MAPK/ERK pathway, Molecular Sequence Data, Polymerase Chain Reaction, p38 Mitogen-Activated Protein Kinases, Proto-Oncogene Proteins c-myc, Humans, Amino Acid Sequence, Phosphorylation, Carbohydrate-responsive element-binding protein, Peptide sequence, Calcium-Calmodulin-Dependent Protein Kinases, Multidisciplinary, Basic helix-loop-helix, biology, Base Sequence, Kinase, Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Helix-Loop-Helix Motifs, Sequence Analysis, DNA, DNA-Binding Proteins, Basic-Leucine Zipper Transcription Factors, Biochemistry, Mitogen-activated protein kinase, biology.protein, Mitogen-Activated Protein Kinases, Protein Binding, Transcription Factors, Research Article
الوصف: 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.
تدمد: 0027-8424
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a634ee8f702af1a10895c01952e442abTest
https://pubmed.ncbi.nlm.nih.gov/7479834Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....a634ee8f702af1a10895c01952e442ab
قاعدة البيانات: OpenAIRE