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1fo6

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(New page: 200px<br /><applet load="1fo6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fo6, resolution 1.95&Aring;" /> '''CRYSTAL STRUCTURE AN...)
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[[Image:1fo6.jpg|left|200px]]<br /><applet load="1fo6" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1fo6, resolution 1.95&Aring;" />
caption="1fo6, resolution 1.95&Aring;" />
'''CRYSTAL STRUCTURE ANALYSIS OF N-CARBAMoYL-D-AMINO-ACID AMIDOHYDROLASE'''<br />
'''CRYSTAL STRUCTURE ANALYSIS OF N-CARBAMoYL-D-AMINO-ACID AMIDOHYDROLASE'''<br />
==Overview==
==Overview==
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The N-carbamoyl-D-amino-acid amidohydrolase (D-NCAase) is used on an, industrial scale for the production of D-amino acids. The crystal, structure of D-NCAase was solved by multiple isomorphous replacement with, anomalous scattering using xenon and gold derivatives, and refined to 1.95, A resolution, to an R-factor of 18.6 %. The crystal structure shows a, four-layer alpha/beta fold with two six-stranded beta sheets packed on, either side by two alpha helices. One exterior layer faces the solvent, whereas the other one is buried and involved in the tight intersubunit, contacts. A long C-terminal fragment extends from a monomer to a site near, a dyad axis, and associates with another monomer to form a small and, hydrophobic cavity, where a xenon atom can bind. Site-directed mutagenesis, of His129, His144 and His215 revealed strict geometric requirements of, these conserved residues to maintain a stable conformation of a putative, catalytic cleft. A region located within this cleft involving Cys172, Glu47, and Lys127 is proposed for D-NCAase catalysis and is similar to the, Cys-Asp-Lys site of N-carbamoylsarcosine amidohydrolase. The homologous, active-site framework of these enzymes with distinct structures suggests, convergent evolution of a common catalytic mechanism.
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The N-carbamoyl-D-amino-acid amidohydrolase (D-NCAase) is used on an industrial scale for the production of D-amino acids. The crystal structure of D-NCAase was solved by multiple isomorphous replacement with anomalous scattering using xenon and gold derivatives, and refined to 1.95 A resolution, to an R-factor of 18.6 %. The crystal structure shows a four-layer alpha/beta fold with two six-stranded beta sheets packed on either side by two alpha helices. One exterior layer faces the solvent, whereas the other one is buried and involved in the tight intersubunit contacts. A long C-terminal fragment extends from a monomer to a site near a dyad axis, and associates with another monomer to form a small and hydrophobic cavity, where a xenon atom can bind. Site-directed mutagenesis of His129, His144 and His215 revealed strict geometric requirements of these conserved residues to maintain a stable conformation of a putative catalytic cleft. A region located within this cleft involving Cys172, Glu47, and Lys127 is proposed for D-NCAase catalysis and is similar to the Cys-Asp-Lys site of N-carbamoylsarcosine amidohydrolase. The homologous active-site framework of these enzymes with distinct structures suggests convergent evolution of a common catalytic mechanism.
==About this Structure==
==About this Structure==
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1FO6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Agrobacterium_tumefaciens Agrobacterium tumefaciens] with XE as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Gamma-glutamyl_hydrolase Gamma-glutamyl hydrolase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.19.9 3.4.19.9] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1FO6 OCA].
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1FO6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Agrobacterium_tumefaciens Agrobacterium tumefaciens] with <scene name='pdbligand=XE:'>XE</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Gamma-glutamyl_hydrolase Gamma-glutamyl hydrolase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.19.9 3.4.19.9] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FO6 OCA].
==Reference==
==Reference==
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[[Category: Gamma-glutamyl hydrolase]]
[[Category: Gamma-glutamyl hydrolase]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Chen, C.Y.]]
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[[Category: Chen, C Y.]]
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[[Category: Chien, F.T.]]
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[[Category: Chien, F T.]]
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[[Category: Hsu, W.H.]]
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[[Category: Hsu, W H.]]
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[[Category: Wang, W.C.]]
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[[Category: Wang, W C.]]
[[Category: XE]]
[[Category: XE]]
[[Category: four layer a/b fold]]
[[Category: four layer a/b fold]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 15:05:10 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:40:46 2008''

Revision as of 10:40, 21 February 2008


1fo6, resolution 1.95Å

Drag the structure with the mouse to rotate

CRYSTAL STRUCTURE ANALYSIS OF N-CARBAMoYL-D-AMINO-ACID AMIDOHYDROLASE

Overview

The N-carbamoyl-D-amino-acid amidohydrolase (D-NCAase) is used on an industrial scale for the production of D-amino acids. The crystal structure of D-NCAase was solved by multiple isomorphous replacement with anomalous scattering using xenon and gold derivatives, and refined to 1.95 A resolution, to an R-factor of 18.6 %. The crystal structure shows a four-layer alpha/beta fold with two six-stranded beta sheets packed on either side by two alpha helices. One exterior layer faces the solvent, whereas the other one is buried and involved in the tight intersubunit contacts. A long C-terminal fragment extends from a monomer to a site near a dyad axis, and associates with another monomer to form a small and hydrophobic cavity, where a xenon atom can bind. Site-directed mutagenesis of His129, His144 and His215 revealed strict geometric requirements of these conserved residues to maintain a stable conformation of a putative catalytic cleft. A region located within this cleft involving Cys172, Glu47, and Lys127 is proposed for D-NCAase catalysis and is similar to the Cys-Asp-Lys site of N-carbamoylsarcosine amidohydrolase. The homologous active-site framework of these enzymes with distinct structures suggests convergent evolution of a common catalytic mechanism.

About this Structure

1FO6 is a Single protein structure of sequence from Agrobacterium tumefaciens with as ligand. Active as Gamma-glutamyl hydrolase, with EC number 3.4.19.9 Full crystallographic information is available from OCA.

Reference

Crystal structure and site-directed mutagenesis studies of N-carbamoyl-D-amino-acid amidohydrolase from Agrobacterium radiobacter reveals a homotetramer and insight into a catalytic cleft., Wang WC, Hsu WH, Chien FT, Chen CY, J Mol Biol. 2001 Feb 16;306(2):251-61. PMID:11237598

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