2rb9

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[[Image:2rb9.jpg|left|200px]]<br /><applet load="2rb9" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:2rb9.jpg|left|200px]]
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caption="2rb9, resolution 2.000&Aring;" />
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'''Crystal structure of E.coli HypE'''<br />
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{{Structure
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|PDB= 2rb9 |SIZE=350|CAPTION= <scene name='initialview01'>2rb9</scene>, resolution 2.000&Aring;
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|SITE=
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|LIGAND=
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|ACTIVITY=
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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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}}
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'''Crystal structure of E.coli HypE'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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2RB9 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli_o157:h7 Escherichia coli o157:h7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2RB9 OCA].
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2RB9 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli_o157:h7 Escherichia coli o157:h7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2RB9 OCA].
==Reference==
==Reference==
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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:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=18065529 18065529]
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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:[http://www.ncbi.nlm.nih.gov/pubmed/18065529 18065529]
[[Category: Escherichia coli o157:h7]]
[[Category: Escherichia coli o157:h7]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: hydrogenase maturation]]
[[Category: hydrogenase maturation]]
[[Category: montreal-kingston bacterial structural genomics initiative]]
[[Category: montreal-kingston bacterial structural genomics initiative]]
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[[Category: structural genomics]]
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[[Category: structural genomic]]
[[Category: unknown function]]
[[Category: unknown function]]
[[Category: x-ray crystallography]]
[[Category: x-ray crystallography]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:46:03 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 18:34:21 2008''

Revision as of 16:34, 20 March 2008


PDB ID 2rb9

Drag the structure with the mouse to rotate
, resolution 2.000Å
Gene: hypE, ECs3586 (Escherichia coli O157:H7)
Coordinates: save as pdb, mmCIF, xml



Crystal structure of E.coli HypE


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.

About this Structure

2RB9 is a Single protein structure of sequence from Escherichia coli o157:h7. Full crystallographic information is available from OCA.

Reference

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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