ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

Unique Utilization of a Phosphoprotein Phosphatase Fold by a Mammalian Phosphodiesterase Associated with WAGR Syndrome

Dermol, Urska and Janardan, Vishnu and Tyagi, Richa and Visweswariah, Sandhya S and Podobnik, Marjetka (2011) Unique Utilization of a Phosphoprotein Phosphatase Fold by a Mammalian Phosphodiesterase Associated with WAGR Syndrome. In: Journal of Molecular Biology, 412 (3). pp. 481-494.

[img] PDF
Unique.pdf - Published Version
Restricted to Registered users only

Download (2115Kb) | Request a copy
Official URL: http://dx.doi.org/10.1016/j.jmb.2011.07.060

Abstract

Metallophosphoesterase-domain-containing protein 2 (MPPED2) is a highly evolutionarily conserved protein with orthologs found from worms to humans. The human MPPED2 gene is found in a region of chromosome 11 that is deleted in patients with WAGR (Wilms tumor, aniridia, genitourinary anomalies, and mental retardation) syndrome, and MPPED2 may function as a tumor suppressor. However, the precise cellular roles of MPPED2 are unknown, and its low phosphodiesterase activity suggests that substrate hydrolysis may not be its prime function. We present here the structures of MPPED2 and two mutants, which show that the poor activity of MPPED2 is not only a consequence of the substitution of an active-site histidine residue by glycine but also due to binding of AMP or GMP to the active site. This feature, enhanced by structural elements of the protein, allows MPPED2 to utilize the conserved phosphoprotein-phosphatase-like fold in a unique manner, ensuring that its enzymatic activity can be combined with a possible role as a scaffolding or adaptor protein. (C) 2011 Elsevier Ltd. All rights reserved.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to Elsevier Science.
Keywords: MPPED2;WAGR syndrome;metallophosphoesterase;phosphoprotein-phosphatase-like fold;AMP/GMP binding
Department/Centre: Division of Biological Sciences > Molecular Reproduction, Development & Genetics (formed by the merger of DBGL and CRBME)
Date Deposited: 04 Nov 2011 09:17
Last Modified: 04 Nov 2011 09:17
URI: http://eprints.iisc.ernet.in/id/eprint/41645

Actions (login required)

View Item View Item