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1mve

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(New page: 200px<br /><applet load="1mve" size="450" color="white" frame="true" align="right" spinBox="true" caption="1mve, resolution 1.70&Aring;" /> '''Crystal structure of...)
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[[Image:1mve.gif|left|200px]]<br /><applet load="1mve" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1mve.gif|left|200px]]<br /><applet load="1mve" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1mve, resolution 1.70&Aring;" />
caption="1mve, resolution 1.70&Aring;" />
'''Crystal structure of a natural circularly-permutated jellyroll protein: 1,3-1,4-beta-D-glucanase from Fibrobacter succinogenes'''<br />
'''Crystal structure of a natural circularly-permutated jellyroll protein: 1,3-1,4-beta-D-glucanase from Fibrobacter succinogenes'''<br />
==Overview==
==Overview==
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The 1,3-1,4-beta-D-glucanase from Fibrobacter succinogenes, (Fsbeta-glucanase) is classified as one of the family 16 glycosyl, hydrolases. It hydrolyzes the glycosidic bond in the mixed-linked glucans, containing beta-1,3- and beta-1,4-glycosidic linkages. We constructed a, truncated form of recombinant Fsbeta-glucanase containing the catalytic, domain from amino acid residues 1-258, which exhibited a higher thermal, stability and enzymatic activity than the full-length enzyme. The crystal, structure of the truncated Fsbeta-glucanase was solved at a resolution of, 1.7A by the multiple wavelength anomalous dispersion (MAD) method using, the anomalous signals from the seleno-methionine-labeled protein. The, overall topology of the truncated Fsbeta-glucanase consists mainly of two, eight-stranded anti-parallel beta-sheets arranged in a jellyroll, beta-sandwich, similar to the fold of many glycosyl hydrolases and, carbohydrate-binding modules. Sequence comparison with other bacterial, glucanases showed that Fsbeta-glucanase is the only naturally occurring, circularly permuted beta-glucanase with reversed sequences. Structural, comparison shows that the engineered circular-permuted Bacillus enzymes, are more similar to their parent enzymes with which they share, approximately 70% sequence identity, than to the naturally occurring, Fsbeta-glucanase of similar topology with 30% identity. This result, suggests that protein structure relies more on sequence identity than, topology. The high-resolution structure of Fsbeta-glucanase provides a, structural rationale for the different activities obtained from a series, of mutant glucanases and a basis for the development of engineered enzymes, with increased activity and structural stability.
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The 1,3-1,4-beta-D-glucanase from Fibrobacter succinogenes (Fsbeta-glucanase) is classified as one of the family 16 glycosyl hydrolases. It hydrolyzes the glycosidic bond in the mixed-linked glucans containing beta-1,3- and beta-1,4-glycosidic linkages. We constructed a truncated form of recombinant Fsbeta-glucanase containing the catalytic domain from amino acid residues 1-258, which exhibited a higher thermal stability and enzymatic activity than the full-length enzyme. The crystal structure of the truncated Fsbeta-glucanase was solved at a resolution of 1.7A by the multiple wavelength anomalous dispersion (MAD) method using the anomalous signals from the seleno-methionine-labeled protein. The overall topology of the truncated Fsbeta-glucanase consists mainly of two eight-stranded anti-parallel beta-sheets arranged in a jellyroll beta-sandwich, similar to the fold of many glycosyl hydrolases and carbohydrate-binding modules. Sequence comparison with other bacterial glucanases showed that Fsbeta-glucanase is the only naturally occurring circularly permuted beta-glucanase with reversed sequences. Structural comparison shows that the engineered circular-permuted Bacillus enzymes are more similar to their parent enzymes with which they share approximately 70% sequence identity, than to the naturally occurring Fsbeta-glucanase of similar topology with 30% identity. This result suggests that protein structure relies more on sequence identity than topology. The high-resolution structure of Fsbeta-glucanase provides a structural rationale for the different activities obtained from a series of mutant glucanases and a basis for the development of engineered enzymes with increased activity and structural stability.
==About this Structure==
==About this Structure==
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1MVE is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Fibrobacter_succinogenes Fibrobacter succinogenes] with CA as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Licheninase Licheninase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.73 3.2.1.73] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1MVE OCA].
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1MVE is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Fibrobacter_succinogenes Fibrobacter succinogenes] with <scene name='pdbligand=CA:'>CA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Licheninase Licheninase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.73 3.2.1.73] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MVE OCA].
==Reference==
==Reference==
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[[Category: Licheninase]]
[[Category: Licheninase]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Lee, S.H.]]
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[[Category: Lee, S H.]]
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[[Category: Lin, S.S.]]
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[[Category: Lin, S S.]]
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[[Category: Shyur, L.F.]]
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[[Category: Shyur, L F.]]
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[[Category: Tsai, L.C.]]
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[[Category: Tsai, L C.]]
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[[Category: Yuan, H.S.]]
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[[Category: Yuan, H S.]]
[[Category: CA]]
[[Category: CA]]
[[Category: circular-permutated jellyroll protein]]
[[Category: circular-permutated jellyroll protein]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 21:43:45 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:59:24 2008''

Revision as of 11:59, 21 February 2008


1mve, resolution 1.70Å

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Crystal structure of a natural circularly-permutated jellyroll protein: 1,3-1,4-beta-D-glucanase from Fibrobacter succinogenes

Overview

The 1,3-1,4-beta-D-glucanase from Fibrobacter succinogenes (Fsbeta-glucanase) is classified as one of the family 16 glycosyl hydrolases. It hydrolyzes the glycosidic bond in the mixed-linked glucans containing beta-1,3- and beta-1,4-glycosidic linkages. We constructed a truncated form of recombinant Fsbeta-glucanase containing the catalytic domain from amino acid residues 1-258, which exhibited a higher thermal stability and enzymatic activity than the full-length enzyme. The crystal structure of the truncated Fsbeta-glucanase was solved at a resolution of 1.7A by the multiple wavelength anomalous dispersion (MAD) method using the anomalous signals from the seleno-methionine-labeled protein. The overall topology of the truncated Fsbeta-glucanase consists mainly of two eight-stranded anti-parallel beta-sheets arranged in a jellyroll beta-sandwich, similar to the fold of many glycosyl hydrolases and carbohydrate-binding modules. Sequence comparison with other bacterial glucanases showed that Fsbeta-glucanase is the only naturally occurring circularly permuted beta-glucanase with reversed sequences. Structural comparison shows that the engineered circular-permuted Bacillus enzymes are more similar to their parent enzymes with which they share approximately 70% sequence identity, than to the naturally occurring Fsbeta-glucanase of similar topology with 30% identity. This result suggests that protein structure relies more on sequence identity than topology. The high-resolution structure of Fsbeta-glucanase provides a structural rationale for the different activities obtained from a series of mutant glucanases and a basis for the development of engineered enzymes with increased activity and structural stability.

About this Structure

1MVE is a Single protein structure of sequence from Fibrobacter succinogenes with as ligand. Active as Licheninase, with EC number 3.2.1.73 Full crystallographic information is available from OCA.

Reference

Crystal structure of a natural circularly permuted jellyroll protein: 1,3-1,4-beta-D-glucanase from Fibrobacter succinogenes., Tsai LC, Shyur LF, Lee SH, Lin SS, Yuan HS, J Mol Biol. 2003 Jul 11;330(3):607-20. PMID:12842475

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