4eng

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(New page: 200px<br /><applet load="4eng" size="450" color="white" frame="true" align="right" spinBox="true" caption="4eng, resolution 1.9&Aring;" /> '''STRUCTURE OF ENDOGLUC...)
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[[Image:4eng.gif|left|200px]]<br /><applet load="4eng" size="350" color="white" frame="true" align="right" spinBox="true"
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caption="4eng, resolution 1.9&Aring;" />
'''STRUCTURE OF ENDOGLUCANASE V CELLOHEXAOSE COMPLEX'''<br />
'''STRUCTURE OF ENDOGLUCANASE V CELLOHEXAOSE COMPLEX'''<br />
==Overview==
==Overview==
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The structure of the catalytic core of the endoglucanase V (EGV) from, Humicola insolens has been determined by the method of multiple, isomorphous replacement at 1.5 A resolution. The final model, refined with, X-PLOR and PROLSQ, has a crystallographic R factor of 0.163 (R(free) =, 0.240) with deviations from stereochemical target values of 0.012 A and, 0.037 degrees for bonds and angles, respectively. The model was further, refined with SHELXL, including anisotropic modelling of the protein-atom, temperature factors, to give a final model with an R factor of 0.105 and, an R(free) of 0.154. The initial isomorphous replacement electron-density, map was poor and uninterpretable but was improved by the use of, synchrotron data collected at a wavelength chosen so as to optimize the f", contribution of the anomalous scattering from the heavy atoms. The, structure of H. insolens EGV consists of a six-stranded beta-barrel, domain, similar to that found in a family of plant defence proteins, linked by a number of disulfide-bonded loop regions. A long open groove, runs across the surface of the enzyme either side of which lie the, catalytic aspartate residues. The 9 A separation of the catalytic, carboxylate groups is consistent with the observation that EGV catalyzes, the hydrolysis of the cellulose, beta(1--&gt;4) links with inversion of, configuration at the anomeric C1 atom. This structure is the first, representative from the glycosyl hydrolase family 45.
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The structure of the catalytic core of the endoglucanase V (EGV) from Humicola insolens has been determined by the method of multiple isomorphous replacement at 1.5 A resolution. The final model, refined with X-PLOR and PROLSQ, has a crystallographic R factor of 0.163 (R(free) = 0.240) with deviations from stereochemical target values of 0.012 A and 0.037 degrees for bonds and angles, respectively. The model was further refined with SHELXL, including anisotropic modelling of the protein-atom temperature factors, to give a final model with an R factor of 0.105 and an R(free) of 0.154. The initial isomorphous replacement electron-density map was poor and uninterpretable but was improved by the use of synchrotron data collected at a wavelength chosen so as to optimize the f" contribution of the anomalous scattering from the heavy atoms. The structure of H. insolens EGV consists of a six-stranded beta-barrel domain, similar to that found in a family of plant defence proteins, linked by a number of disulfide-bonded loop regions. A long open groove runs across the surface of the enzyme either side of which lie the catalytic aspartate residues. The 9 A separation of the catalytic carboxylate groups is consistent with the observation that EGV catalyzes the hydrolysis of the cellulose, beta(1--&gt;4) links with inversion of configuration at the anomeric C1 atom. This structure is the first representative from the glycosyl hydrolase family 45.
==About this Structure==
==About this Structure==
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4ENG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Humicola_insolens Humicola insolens] with CTR as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Cellulase Cellulase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.4 3.2.1.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=4ENG OCA].
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4ENG is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Humicola_insolens Humicola insolens] with <scene name='pdbligand=CTR:'>CTR</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Cellulase Cellulase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.4 3.2.1.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4ENG OCA].
==Reference==
==Reference==
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[[Category: Humicola insolens]]
[[Category: Humicola insolens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Davies, G.J.]]
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[[Category: Davies, G J.]]
[[Category: Schulein, M.]]
[[Category: Schulein, M.]]
[[Category: CTR]]
[[Category: CTR]]
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[[Category: hydrolase]]
[[Category: hydrolase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 19:32:59 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 19:13:08 2008''

Revision as of 17:13, 21 February 2008


4eng, resolution 1.9Å

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STRUCTURE OF ENDOGLUCANASE V CELLOHEXAOSE COMPLEX

Overview

The structure of the catalytic core of the endoglucanase V (EGV) from Humicola insolens has been determined by the method of multiple isomorphous replacement at 1.5 A resolution. The final model, refined with X-PLOR and PROLSQ, has a crystallographic R factor of 0.163 (R(free) = 0.240) with deviations from stereochemical target values of 0.012 A and 0.037 degrees for bonds and angles, respectively. The model was further refined with SHELXL, including anisotropic modelling of the protein-atom temperature factors, to give a final model with an R factor of 0.105 and an R(free) of 0.154. The initial isomorphous replacement electron-density map was poor and uninterpretable but was improved by the use of synchrotron data collected at a wavelength chosen so as to optimize the f" contribution of the anomalous scattering from the heavy atoms. The structure of H. insolens EGV consists of a six-stranded beta-barrel domain, similar to that found in a family of plant defence proteins, linked by a number of disulfide-bonded loop regions. A long open groove runs across the surface of the enzyme either side of which lie the catalytic aspartate residues. The 9 A separation of the catalytic carboxylate groups is consistent with the observation that EGV catalyzes the hydrolysis of the cellulose, beta(1-->4) links with inversion of configuration at the anomeric C1 atom. This structure is the first representative from the glycosyl hydrolase family 45.

About this Structure

4ENG is a Single protein structure of sequence from Humicola insolens with as ligand. Active as Cellulase, with EC number 3.2.1.4 Full crystallographic information is available from OCA.

Reference

Structure determination and refinement of the Humicola insolens endoglucanase V at 1.5 A resolution., Davies GJ, Dodson G, Moore MH, Tolley SP, Dauter Z, Wilson KS, Rasmussen G, Schulein M, Acta Crystallogr D Biol Crystallogr. 1996 Jan 1;52(Pt 1):7-17. PMID:15299721

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