Identification and structural characterization of two 14-3-3 binding sites in the human peptidylarginine deiminase type VI.

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Citation

Rose R, Rose M, Ottmann C

Identification and structural characterization of two 14-3-3 binding sites in the human peptidylarginine deiminase type VI.

J Struct Biol. 2012 Oct;180(1):65-72. doi: 10.1016/j.jsb.2012.05.010. Epub 2012 May 24.

PubMed ID
22634725 [ View in PubMed
]
Abstract

The regulation and function of peptidylarginine deiminase isoform VI (PAD6), which is a highly abundant protein associated with the cytoplasmic lattices in mammalian oocytes, is poorly understood so far. It has been shown previously, that 14-3-3 proteins, a class of regulatory adapter proteins ubiquitous in eukaryotes, bind to PAD6 in vivo in a phosphorylation dependent manner. Here we identify possible 14-3-3 binding sites in human PAD6 by in silico methods, looking for conserved, surface exposed serine residues. Two of these sites were confirmed as 14-3-3 binding sites by fluorescence polarization competition and X-ray crystallography. We furthermore suggest a role of RSK-type kinases in the phosphorylation of one of these two binding sites and provide evidence in the form of in vitro kinase assays with p70S6 kinase and RSK1.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Protein-arginine deiminase type-6Q6TGC4Details