2bjh

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[[Image:2bjh.gif|left|200px]]<br /><applet load="2bjh" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:2bjh.gif|left|200px]]
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caption="2bjh, resolution 2.54&Aring;" />
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'''CRYSTAL STRUCTURE OF S133A ANFAEA-FERULIC ACID COMPLEX'''<br />
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{{Structure
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|PDB= 2bjh |SIZE=350|CAPTION= <scene name='initialview01'>2bjh</scene>, resolution 2.54&Aring;
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|SITE= <scene name='pdbsite=AC1:Fer+Binding+Site+For+Chain+C'>AC1</scene>
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|LIGAND= <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=NDG:2-(ACETYLAMINO)-2-DEOXY-A-D-GLUCOPYRANOSE'>NDG</scene> and <scene name='pdbligand=FER:3-(4-HYDROXY-3-METHOXYPHENYL)-2-PROPENOIC ACID'>FER</scene>
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|ACTIVITY= [http://en.wikipedia.org/wiki/Feruloyl_esterase Feruloyl esterase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.1.73 3.1.1.73]
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|GENE=
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}}
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'''CRYSTAL STRUCTURE OF S133A ANFAEA-FERULIC ACID COMPLEX'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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2BJH is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Aspergillus_niger Aspergillus niger] with <scene name='pdbligand=NAG:'>NAG</scene>, <scene name='pdbligand=NDG:'>NDG</scene> and <scene name='pdbligand=FER:'>FER</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Feruloyl_esterase Feruloyl esterase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.1.73 3.1.1.73] Known structural/functional Site: <scene name='pdbsite=AC1:Fer+Binding+Site+For+Chain+C'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2BJH OCA].
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2BJH is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Aspergillus_niger Aspergillus niger]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2BJH OCA].
==Reference==
==Reference==
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Probing the determinants of substrate specificity of a feruloyl esterase, AnFaeA, from Aspergillus niger., Faulds CB, Molina R, Gonzalez R, Husband F, Juge N, Sanz-Aparicio J, Hermoso JA, FEBS J. 2005 Sep;272(17):4362-71. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=16128806 16128806]
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Probing the determinants of substrate specificity of a feruloyl esterase, AnFaeA, from Aspergillus niger., Faulds CB, Molina R, Gonzalez R, Husband F, Juge N, Sanz-Aparicio J, Hermoso JA, FEBS J. 2005 Sep;272(17):4362-71. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16128806 16128806]
[[Category: Aspergillus niger]]
[[Category: Aspergillus niger]]
[[Category: Feruloyl esterase]]
[[Category: Feruloyl esterase]]
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[[Category: NAG]]
[[Category: NAG]]
[[Category: NDG]]
[[Category: NDG]]
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[[Category: degradation plant cell walls]]
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[[Category: degradation plant cell wall]]
[[Category: feruloyl esterase]]
[[Category: feruloyl esterase]]
[[Category: glycoprotein]]
[[Category: glycoprotein]]
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[[Category: xylan degradation]]
[[Category: xylan degradation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:38:27 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:02:44 2008''

Revision as of 14:02, 20 March 2008


PDB ID 2bjh

Drag the structure with the mouse to rotate
, resolution 2.54Å
Sites:
Ligands: , and
Activity: Feruloyl esterase, with EC number 3.1.1.73
Coordinates: save as pdb, mmCIF, xml



CRYSTAL STRUCTURE OF S133A ANFAEA-FERULIC ACID COMPLEX


Overview

Feruloyl esterases hydrolyse phenolic groups involved in the cross-linking of arabinoxylan to other polymeric structures. This is important for opening the cell wall structure making material more accessible to glycoside hydrolases. Here we describe the crystal structure of inactive S133A mutant of type-A feruloyl esterase from Aspergillus niger (AnFaeA) in complex with a feruloylated trisaccharide substrate. Only the ferulic acid moiety of the substrate is visible in the electron density map, showing interactions through its OH and OCH(3) groups with the hydroxyl groups of Tyr80. The importance of aromatic and polar residues in the activity of AnFaeA was also evaluated using site-directed mutagenesis. Four mutant proteins were heterologously expressed in Pichia pastoris, and their kinetic properties determined against methyl esters of ferulic, sinapic, caffeic and p-coumaric acid. The k(cat) of Y80S, Y80V, W260S and W260V was drastically reduced compared to that of the wild-type enzyme. However, the replacement of Tyr80 and Trp260 with smaller residues broadened the substrate specificity of the enzyme, allowing the hydrolysis of methyl caffeate. The role of Tyr80 and Trp260 in AnFaeA are discussed in light of the three-dimensional structure.

About this Structure

2BJH is a Single protein structure of sequence from Aspergillus niger. Full crystallographic information is available from OCA.

Reference

Probing the determinants of substrate specificity of a feruloyl esterase, AnFaeA, from Aspergillus niger., Faulds CB, Molina R, Gonzalez R, Husband F, Juge N, Sanz-Aparicio J, Hermoso JA, FEBS J. 2005 Sep;272(17):4362-71. PMID:16128806

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