2i6r: Difference between revisions

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[[Image:2i6r.jpg|left|200px]]
[[Image:2i6r.jpg|left|200px]]


{{Structure
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|GENE= hypE, ECs3586 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=83334 Escherichia coli O157:H7])
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|DOMAIN=
{{STRUCTURE_2i6r| PDB=2i6r |  SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2i6r FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2i6r OCA], [http://www.ebi.ac.uk/pdbsum/2i6r PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2i6r RCSB]</span>
}}


'''Crystal structure of E. coli HypE, a hydrogenase maturation protein'''
'''Crystal structure of E. coli HypE, a hydrogenase maturation protein'''
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[[Category: Proteau, A.]]
[[Category: Proteau, A.]]
[[Category: Rangarajan, E S.]]
[[Category: Rangarajan, E S.]]
[[Category: bsgi]]
[[Category: Bsgi]]
[[Category: hydrogenase maturation protein]]
[[Category: Hydrogenase maturation protein]]
[[Category: hype]]
[[Category: Hype]]
[[Category: montreal-kingston bacterial structural genomics initiative]]
[[Category: Montreal-kingston bacterial structural genomics initiative]]
[[Category: structural genomic]]
[[Category: Structural genomic]]
[[Category: unknown function]]
[[Category: Unknown function]]
 
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Revision as of 07:08, 4 May 2008

File:2i6r.jpg

Template:STRUCTURE 2i6r

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


OverviewOverview

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.

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 Page seeded by OCA on Sun May 4 07:08:43 2008

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