1hgw: Difference between revisions

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[[Image:1hgw.jpg|left|200px]]
[[Image:1hgw.jpg|left|200px]]


{{Structure
<!--
|PDB= 1hgw |SIZE=350|CAPTION= <scene name='initialview01'>1hgw</scene>, resolution 2.10&Aring;
The line below this paragraph, containing "STRUCTURE_1hgw", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)  
|LIGAND= <scene name='pdbligand=CO:COBALT+(II)+ION'>CO</scene>, <scene name='pdbligand=MAN:ALPHA-D-MANNOSE'>MAN</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Cellulose_1,4-beta-cellobiosidase Cellulose 1,4-beta-cellobiosidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.91 3.2.1.91] </span>
or leave the SCENE parameter empty for the default display.
|GENE= CBH2 (D175A) ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=51453 Hypocrea jecorina])
-->
|DOMAIN=
{{STRUCTURE_1hgw| PDB=1hgw |  SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1hgw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1hgw OCA], [http://www.ebi.ac.uk/pdbsum/1hgw PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1hgw RCSB]</span>
}}


'''CEL6A D175A MUTANT'''
'''CEL6A D175A MUTANT'''
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[[Category: Jones, T A.]]
[[Category: Jones, T A.]]
[[Category: Zou, J Y.]]
[[Category: Zou, J Y.]]
[[Category: glycoprotein]]
[[Category: Glycoprotein]]
[[Category: glycosidase]]
[[Category: Glycosidase]]
[[Category: hydrolase (o-glycosyl)]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May  2 18:50:03 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:04:43 2008''

Revision as of 18:50, 2 May 2008

File:1hgw.jpg

Template:STRUCTURE 1hgw

CEL6A D175A MUTANT


OverviewOverview

Trichoderma reesei cellobiohydrolase Cel6A is an inverting glycosidase. Structural studies have established that the tunnel-shaped active site of Cel6A contains two aspartic acids, D221 and D175, that are close to the glycosidic oxygen of the scissile bond and at hydrogen-bonding distance from each other. Here, site-directed mutagenesis, X-ray crystallography, and enzyme kinetic studies have been used to confirm the role of residue D221 as the catalytic acid. D175 is shown to affect protonation of D221 and to contribute to the electrostatic stabilization of the partial positive charge in the transition state. Structural and modeling studies suggest that the single-displacement mechanism of Cel6A may not directly involve a catalytic base. The value of (D2O)(V) of 1.16 +/- 0.14 for hydrolysis of cellotriose suggests that the large direct effect expected for proton transfer from the nucleophilic water through a water chain (Grotthus mechanism) is offset by an inverse effect arising from reversibly breaking the short, tight hydrogen bond between D221 and D175 before catalysis.

About this StructureAbout this Structure

1HGW is a Single protein structure of sequence from Hypocrea jecorina. Full crystallographic information is available from OCA.

ReferenceReference

The active site of cellobiohydrolase Cel6A from Trichoderma reesei: the roles of aspartic acids D221 and D175., Koivula A, Ruohonen L, Wohlfahrt G, Reinikainen T, Teeri TT, Piens K, Claeyssens M, Weber M, Vasella A, Becker D, Sinnott ML, Zou JY, Kleywegt GJ, Szardenings M, Stahlberg J, Jones TA, J Am Chem Soc. 2002 Aug 28;124(34):10015-24. PMID:12188666 Page seeded by OCA on Fri May 2 18:50:03 2008

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