2i6r: Difference between revisions

Revision as of 02:16, 28 July 2008

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:2i6r.png

Template:STRUCTURE 2i6r

Crystal structure of E. coli HypE, a hydrogenase maturation proteinCrystal structure of E. coli HypE, a hydrogenase maturation protein

Template:ABSTRACT PUBMED 18065529

About this StructureAbout this Structure

2I6R is a Single protein structure of sequence from Escherichia coli o157:h7. Full crystallographic information is available from OCA.

ReferenceReference

Structure of [NiFe] hydrogenase maturation protein HypE from Escherichia coli and its interaction with HypF., Rangarajan ES, Asinas A, Proteau A, Munger C, Baardsnes J, Iannuzzi P, Matte A, Cygler M, J Bacteriol. 2008 Feb;190(4):1447-58. Epub 2007 Dec 7. PMID:18065529

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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

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-'''Crystal structure of E. coli HypE, a hydrogenase maturation protein'''
+===Crystal structure of E. coli HypE, a hydrogenase maturation protein===
-==Overview==
+<!--
-Hydrogenases are enzymes involved in hydrogen metabolism, utilizing H2 as an electron source. [NiFe] hydrogenases are heterodimeric Fe-S proteins, with a large subunit containing the reaction center involving Fe and Ni metal ions and a small subunit containing one or more Fe-S clusters. Maturation of the [NiFe] hydrogenase involves assembly of nonproteinaceous ligands on the large subunit by accessory proteins encoded by the hyp operon. HypE is an essential accessory protein and participates in the synthesis of two cyano groups found in the large subunit. We report the crystal structure of Escherichia coli HypE at 2.0-A resolution. HypE exhibits a fold similar to that of PurM and ThiL and forms dimers. The C-terminal catalytically essential Cys336 is internalized at the dimer interface between the N- and C-terminal domains. A mechanism for dehydration of the thiocarbamate to the thiocyanate is proposed, involving Asp83 and Glu272. The interactions of HypE and HypF were characterized in detail by surface plasmon resonance and isothermal titration calorimetry, revealing a Kd (dissociation constant) of approximately 400 nM. The stoichiometry and molecular weights of the complex were verified by size exclusion chromatography and gel scanning densitometry. These experiments reveal that HypE and HypF associate to form a stoichiometric, hetero-oligomeric complex predominantly consisting of a [EF]2 heterotetramer which exists in a dynamic equilibrium with the EF heterodimer. The surface plasmon resonance results indicate that a conformational change occurs upon heterodimerization which facilitates formation of a productive complex as part of the carbamate transfer reaction.
+The line below this paragraph, {{ABSTRACT_PUBMED_18065529}}, adds the Publication Abstract to the page
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+{{ABSTRACT_PUBMED_18065529}}
 ==About this Structure==
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 [[Category: Structural genomic]]
 [[Category: Unknown function]]
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