A novel protein kinase with leucine zipper-like sequences: its catalytic domain is highly homologous to that of protein kinase C

Biochem Biophys Res Commun. 1994 Mar 15;199(2):897-904. doi: 10.1006/bbrc.1994.1313.

Abstract

A novel protein kinase, designated PKN, was identified by molecular cloning from a human hippocampus cDNA library. PKN consists of 942 amino acids with a calculated molecular mass of 103,925 daltons. PKN has leucine zipper-like sequences in its amino terminal region and contains a catalytic domain that shows strong similarity to that of protein kinase C family. Northern blot analysis indicates PKN is expressed ubiquitously in human tissues. Antisera against PKN identified a 120K dalton protein on SDS polyacrylamide gel electrophoresis when PKN was expressed in the insect cells or COS7 cells. Recombinant PKN revealed an intrinsic protein kinase activity associated with a 120K protein. This activity was abolished by mutation of the lysine residue in the potential ATP binding site.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Binding Sites
  • Blotting, Northern
  • Cell Line
  • Cloning, Molecular
  • Gene Expression
  • Gene Library
  • Hippocampus / enzymology*
  • Humans
  • Leucine Zippers*
  • Molecular Sequence Data
  • Molecular Weight
  • Moths
  • Mutagenesis, Site-Directed
  • Protein Kinase C / chemistry*
  • Protein Serine-Threonine Kinases*
  • Protein-Tyrosine Kinases / biosynthesis
  • Protein-Tyrosine Kinases / chemistry*
  • Protein-Tyrosine Kinases / metabolism*
  • Sequence Homology, Amino Acid
  • Transfection

Substances

  • protein kinase N
  • Protein-Tyrosine Kinases
  • Protein Serine-Threonine Kinases
  • Protein Kinase C

Associated data

  • GENBANK/D26180
  • GENBANK/D26181