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Proc Natl Acad Sci U S A. 2013 Jun 25;110(26):10574-9. doi: 10.1073/pnas.1309211110. Epub 2013 Jun 10.

Crystal structure of the Golgi casein kinase.

Author information

1
Department of Pharmacology, University of California at San Diego, La Jolla, CA 92093, USA.

Abstract

The family with sequence similarity 20 (Fam20) kinases phosphorylate extracellular substrates and play important roles in biomineralization. Fam20C is the Golgi casein kinase that phosphorylates secretory pathway proteins within Ser-x-Glu/pSer motifs. Mutations in Fam20C cause Raine syndrome, an osteosclerotic bone dysplasia. Here we report the crystal structure of the Fam20C ortholog from Caenorhabditis elegans. The nucleotide-free and Mn/ADP-bound structures unveil an atypical protein kinase-like fold and highlight residues critical for activity. The position of the regulatory αC helix and the lack of an activation loop indicate an architecture primed for efficient catalysis. Furthermore, several distinct elements, including the presence of disulfide bonds, suggest that the Fam20 family diverged early in the evolution of the protein kinase superfamily. Our results reinforce the structural diversity of protein kinases and have important implications for patients with disorders of biomineralization.

KEYWORDS:

Fam20A; Fam20B; amelogenesis imperfecta; enamel renal syndrome; hypophosphatemia

PMID:
23754375
PMCID:
PMC3696822
DOI:
10.1073/pnas.1309211110
[Indexed for MEDLINE]
Free PMC Article

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