| Literature DB >> 18331838 |
Koji Ikegami1, Daisuke Horigome, Masahiro Mukai, Itamar Livnat, Grant R MacGregor, Mitsutoshi Setou.
Abstract
Certain proteins can undergo polyglycylation and polyglutamylation. Polyglutamylases (glutamate ligases) have recently been identified in a family of tubulin tyrosine ligase-like (TTLL) proteins. However, no polyglycylase (glycine ligase) has yet been reported. Here we identify a polyglycylase in the TTLL proteins by using an anti-poly-glycine antibody. The antibody reacted with a cytoplasmic 60-kDa protein that accumulated in elongating spermatids. Using tandem mass spectrometry of trypsinized samples, immunoprecipitated by the antibody from the TTLL10-expressing cells, we identified the 60-kDa protein as nucleosome assembly protein 1 (NAP1). Recombinant TTLL10 incorporated glycine into recombinant NAP1 in vitro. Mutational analyses indicated that Glu residues at 359 and 360 in the C-terminal part of NAP1 are putative sites for the modification. Thus, TTLL10 is a polyglycylase for NAP1.Entities:
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Year: 2008 PMID: 18331838 PMCID: PMC2408875 DOI: 10.1016/j.febslet.2008.02.079
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124