2jer

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2jer, resolution 1.65Å

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AGMATINE DEIMINASE OF ENTEROCOCCUS FAECALIS CATALYZING ITS REACTION.

Overview

Enterococcus faecalis makes ATP from agmatine in three steps catalyzed by, agmatine deiminase (AgDI), putrescine transcarbamylase (PTC), and, carbamate kinase (CK). An antiporter exchanges putrescine for agmatine. We, have cloned the E. faecalis ef0732 and ef0734 genes of the reported gene, cluster for agmatine catabolism, overexpressed them in Escherichia coli, purified the products, characterized them functionally as PTC and AgDI, and crystallized and X-ray diffracted them. The 1.65-Angstroms-resolution, structure of AgDI forming a covalent adduct with an agmatine-derived, amidine reactional intermediate is described. We provide definitive, identification of the gene cluster for agmatine catabolism and confirm, that ornithine is a genuine but poor PTC substrate, suggesting that PTC, (found here to be trimeric) evolved from ornithine transcarbamylase., N-(Phosphonoacetyl)-putrescine was prepared and shown to strongly (K(i) =, 10 nM) and selectively inhibit PTC and to improve PTC crystallization. We, find that E. faecalis AgDI, which is committed to ATP generation, closely, resembles the AgDIs involved in making polyamines, suggesting the, recruitment of a polyamine-synthesizing AgDI into the AgDI pathway. The, arginine deiminase (ADI) pathway of arginine catabolism probably supplied, the genes for PTC and CK but not those for the agmatine/putrescine, antiporter, and thus the AgDI and ADI pathways are not related by a single, "en bloc" duplication event. The AgDI crystal structure reveals a tetramer, with a five-blade propeller subunit fold, proves that AgDI closely, resembles ADI despite a lack of sequence identity, and explains substrate, affinity, selectivity, and Cys357-mediated-covalent catalysis. A, three-tongued agmatine-triggered gating opens or blocks access to the, active center.

About this Structure

2JER is a Single protein structure of sequence from Enterococcus faecalis with and as ligands. This structure superseeds the now removed PDB entry 2J2T. Active as Agmatine deiminase, with EC number 3.5.3.12 Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

The gene cluster for agmatine catabolism of Enterococcus faecalis: study of recombinant putrescine transcarbamylase and agmatine deiminase and a snapshot of agmatine deiminase catalyzing its reaction., Llacer JL, Polo LM, Tavarez S, Alarcon B, Hilario R, Rubio V, J Bacteriol. 2007 Feb;189(4):1254-65. Epub 2006 Oct 6. PMID:17028272

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