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2g3n

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(New page: 200px<br /><applet load="2g3n" size="450" color="white" frame="true" align="right" spinBox="true" caption="2g3n, resolution 2.55&Aring;" /> '''Crystal structure of...)
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[[Image:2g3n.gif|left|200px]]<br /><applet load="2g3n" size="350" color="white" frame="true" align="right" spinBox="true"
caption="2g3n, resolution 2.55&Aring;" />
caption="2g3n, resolution 2.55&Aring;" />
'''Crystal structure of the Sulfolobus solfataricus alpha-glucosidase MalA in complex with beta-octyl-glucopyranoside'''<br />
'''Crystal structure of the Sulfolobus solfataricus alpha-glucosidase MalA in complex with beta-octyl-glucopyranoside'''<br />
==Overview==
==Overview==
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The crystal structure of alpha-glucosidase MalA from Sulfolobus, solfataricus has been determined at 2.5Angstrom resolution. It provides a, structural model for enzymes representing the major specificity in, glycoside hydrolase family 31 (GH31), including alpha-glucosidases from, higher organisms, involved in glycogen degradation and glycoprotein, processing. The structure of MalA shows clear differences from the only, other structure known from GH31, alpha-xylosidase YicI. MalA and YicI, share only 23% sequence identity. Although the two enzymes display a, similar domain structure and both form hexamers, their structures differ, significantly in quaternary organization: MalA is a dimer of trimers, YicI, a trimer of dimers. MalA and YicI also differ in their substrate, specificities, as shown by kinetic measurements on model chromogenic, substrates. In addition, MalA has a clear preference for maltose, (Glc-alpha1,4-Glc), whereas YicI prefers isoprimeverose, (Xyl-alpha1,6-Glc). The structural origin of this difference occurs in the, -1 subsite where MalA residues Asp251 and Trp284 could interact with OH6, of the substrate. The structure of MalA in complex with, beta-octyl-glucopyranoside has been determined. It reveals Arg400, Asp87, Trp284, Met321 and Phe327 as invariant residues forming the +1 subsite in, the GH31 alpha-glucosidases. Structural comparisons with other GH families, suggest that the GH31 enzymes belong to clan GH-D.
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The crystal structure of alpha-glucosidase MalA from Sulfolobus solfataricus has been determined at 2.5Angstrom resolution. It provides a structural model for enzymes representing the major specificity in glycoside hydrolase family 31 (GH31), including alpha-glucosidases from higher organisms, involved in glycogen degradation and glycoprotein processing. The structure of MalA shows clear differences from the only other structure known from GH31, alpha-xylosidase YicI. MalA and YicI share only 23% sequence identity. Although the two enzymes display a similar domain structure and both form hexamers, their structures differ significantly in quaternary organization: MalA is a dimer of trimers, YicI a trimer of dimers. MalA and YicI also differ in their substrate specificities, as shown by kinetic measurements on model chromogenic substrates. In addition, MalA has a clear preference for maltose (Glc-alpha1,4-Glc), whereas YicI prefers isoprimeverose (Xyl-alpha1,6-Glc). The structural origin of this difference occurs in the -1 subsite where MalA residues Asp251 and Trp284 could interact with OH6 of the substrate. The structure of MalA in complex with beta-octyl-glucopyranoside has been determined. It reveals Arg400, Asp87, Trp284, Met321 and Phe327 as invariant residues forming the +1 subsite in the GH31 alpha-glucosidases. Structural comparisons with other GH families suggest that the GH31 enzymes belong to clan GH-D.
==About this Structure==
==About this Structure==
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2G3N is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Sulfolobus_solfataricus Sulfolobus solfataricus] with BOG as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Alpha-glucosidase Alpha-glucosidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.20 3.2.1.20] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2G3N OCA].
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2G3N is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Sulfolobus_solfataricus Sulfolobus solfataricus] with <scene name='pdbligand=BOG:'>BOG</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Alpha-glucosidase Alpha-glucosidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.20 3.2.1.20] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2G3N OCA].
==Reference==
==Reference==
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[[Category: Sulfolobus solfataricus]]
[[Category: Sulfolobus solfataricus]]
[[Category: Blum, P.]]
[[Category: Blum, P.]]
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[[Category: Ernst, H.A.]]
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[[Category: Ernst, H A.]]
[[Category: Larsen, S.]]
[[Category: Larsen, S.]]
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[[Category: Leggio, L.Lo.]]
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[[Category: Leggio, L Lo.]]
[[Category: Leonard, G.]]
[[Category: Leonard, G.]]
[[Category: Willemoes, M.]]
[[Category: Willemoes, M.]]
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[[Category: retaining mechanism]]
[[Category: retaining mechanism]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 10:55:56 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:27:45 2008''

Revision as of 15:27, 21 February 2008


2g3n, resolution 2.55Å

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Crystal structure of the Sulfolobus solfataricus alpha-glucosidase MalA in complex with beta-octyl-glucopyranoside

Overview

The crystal structure of alpha-glucosidase MalA from Sulfolobus solfataricus has been determined at 2.5Angstrom resolution. It provides a structural model for enzymes representing the major specificity in glycoside hydrolase family 31 (GH31), including alpha-glucosidases from higher organisms, involved in glycogen degradation and glycoprotein processing. The structure of MalA shows clear differences from the only other structure known from GH31, alpha-xylosidase YicI. MalA and YicI share only 23% sequence identity. Although the two enzymes display a similar domain structure and both form hexamers, their structures differ significantly in quaternary organization: MalA is a dimer of trimers, YicI a trimer of dimers. MalA and YicI also differ in their substrate specificities, as shown by kinetic measurements on model chromogenic substrates. In addition, MalA has a clear preference for maltose (Glc-alpha1,4-Glc), whereas YicI prefers isoprimeverose (Xyl-alpha1,6-Glc). The structural origin of this difference occurs in the -1 subsite where MalA residues Asp251 and Trp284 could interact with OH6 of the substrate. The structure of MalA in complex with beta-octyl-glucopyranoside has been determined. It reveals Arg400, Asp87, Trp284, Met321 and Phe327 as invariant residues forming the +1 subsite in the GH31 alpha-glucosidases. Structural comparisons with other GH families suggest that the GH31 enzymes belong to clan GH-D.

About this Structure

2G3N is a Single protein structure of sequence from Sulfolobus solfataricus with as ligand. Active as Alpha-glucosidase, with EC number 3.2.1.20 Full crystallographic information is available from OCA.

Reference

Structure of the Sulfolobus solfataricus alpha-glucosidase: implications for domain conservation and substrate recognition in GH31., Ernst HA, Lo Leggio L, Willemoes M, Leonard G, Blum P, Larsen S, J Mol Biol. 2006 May 12;358(4):1106-24. Epub 2006 Mar 13. PMID:16580018

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