1zd3

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File:1zd3.gif


1zd3, resolution 2.3Å

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Human soluble epoxide hydrolase 4-(3-cyclohexyluriedo)-butyric acid complex

OverviewOverview

X-ray crystal structures of human soluble epoxide hydrolase (sEH), complexed with four different dialkylurea inhibitors bearing pendant, carboxylate "tails" of varying length have been determined at 2.3-3.0 A, resolution. Similarities among inhibitor binding modes reinforce the, proposed roles of Y381 and/or Y465 as general acids that protonate the, epoxide ring of the substrate in concert with nucleophilic attack of D333, at the electrophilic epoxide carbon. Additionally, the binding of these, inhibitors allows us to model the binding mode of the endogenous substrate, 14,15-epoxyeicosatrienoic acid. Contrasts among inhibitor binding modes, include opposite orientations of inhibitor binding in the active-site, hydrophobic tunnel. Alternative binding orientations observed for this, series of inhibitors to human sEH, as well as the binding of certain, dialkylurea inhibitors to human sEH and murine sEH, complicate the, structure-based design of human sEH inhibitors with potential, pharmaceutical applications in the treatment of hypertension. Thus, with, regard to the optimization of inhibitor designs targeting human sEH, it is, critical that human sEH and not murine sEH be utilized for inhibitor, screening, and it is critical that structures of human sEH-inhibitor, complexes be determined to verify inhibitor binding orientations that, correlate with measured affinities.

DiseaseDisease

Known disease associated with this structure: Hypercholesterolemia, familial, due to LDLR defect, modifier of OMIM:[132811]

About this StructureAbout this Structure

1ZD3 is a Single protein structure of sequence from Homo sapiens with MG, PO4, 15P and NC4 as ligands. Active as Microsomal epoxide hydrolase, with EC number 3.3.2.9 Full crystallographic information is available from OCA.

ReferenceReference

Human soluble epoxide hydrolase: structural basis of inhibition by 4-(3-cyclohexylureido)-carboxylic acids., Gomez GA, Morisseau C, Hammock BD, Christianson DW, Protein Sci. 2006 Jan;15(1):58-64. Epub 2005 Dec 1. PMID:16322563

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