2no6

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spinqualitylabelsall models 2no6, resolution 1.90Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image

C4S dCK variant of dCK in complex with FTC+ADP

Overview

Biological molecules are predominantly enantioselective. Yet currently two, nucleoside analogue prodrugs (3TC and FTC) with opposite chirality, compared to physiological nucleosides are clinically approved for the, treatment of HIV infections. These prodrugs require conversion to their, triphosphorylated forms to achieve pharmacological activity. The first, step in the activation of these agents is catalyzed by human deoxycytidine, kinase (dCK). This enzyme possesses the ability to phosphorylate, nucleosides of the unnatural l-chirality. To understand the molecular, basis for the nonenantioselectivity of dCK, we solved the crystal, structures of the enzyme in complex with the l-enantiomer and of its, physiological substrate deoxycytidine and with the l-nucleoside analogue, FTC. These were compared to a structure solved with d-dC. Our results, highlight structural adjustments imposed on the l-nucleosides and, properties of the enzyme endowing it with the ability to phosphorylate, substrates with nonphysiological chirality. This work reveals the, molecular basis for the activation of l-nucleosides by dCK.

About this Structure

2NO6 is a Single protein structure of sequence from Homo sapiens with ADP and ETV as ligands. Active as Deoxycytidine kinase, with EC number 2.7.1.74 Full crystallographic information is available from OCA.

Reference

Nonenantioselectivity Property of Human Deoxycytidine Kinase Explained by Structures of the Enzyme in Complex with l- and d-Nucleosides., Sabini E, Hazra S, Konrad M, Lavie A, J Med Chem. 2007 Jun 28;50(13):3004-14. Epub 2007 May 27. PMID:17530837

Page seeded by OCA on Mon Nov 12 23:00:35 2007